Using genomics to predict disease risk / en Genetic risk prediction for 10 chronic diseases moves closer to the clinic /news/genetic-risk-prediction-10-chronic-diseases-moves-closer-clinic <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> <span class="field field--name-uid field--type-entity-reference field--label-hidden"> <span>By Corie Lok</span> </span> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" class="datetime">February 19, 2024</time> </span> <div class="hero-section container"> <div class="hero-section__row row"> <div class="hero-section__content hero-section__content_left col-6"> <div class="hero-section__breadcrumbs"> <div class="block block-system block-system-breadcrumb-block"> <nav class="breadcrumb" role="navigation" aria-labelledby="system-breadcrumb"> <h2 id="system-breadcrumb" class="visually-hidden">Breadcrumb</h2> <ol> <li> <a href="/">Home</a> </li> <li> <a href="/news">News</a> </li> </ol> </nav> </div> </div> <div class="hero-section__title"> <div class="block block-layout-builder block-field-blocknodelong-storytitle"> <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> </div> </div> <div class="hero-section__description"> <div class="block block-layout-builder block-field-blocknodelong-storybody"> <div class="clearfix text-formatted field field--name-body field--type-text-with-summary field--label-hidden field__item"><p>As part of a nationwide collaboration, ӳý Clinical Labs researchers have optimized 10 polygenic scores for use in clinical research as part of a study on how to implement genetic risk prediction for patients.</p> </div> </div> </div> <div class="hero-section__author"> <div class="block block-layout-builder block-extra-field-blocknodelong-storyextra-field-author-custom"> By Sarah C.P. Williams </div> </div> <div class="hero-section__date"> <div class="block block-layout-builder block-field-blocknodelong-storycreated"> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" title="Monday, February 19, 2024 - 11:00" class="datetime">February 19, 2024</time> </span> </div> </div> </div> <div class="hero-section__right col-6"> <div class="hero-section__image"> <div class="block block-layout-builder block-field-blocknodelong-storyfield-image"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"> <article class="media media--type-image media--view-mode-multiple-content-types-header"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <picture> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1921px)" type="image/png" 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class="field__item"><article about="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=v0H61Dlb 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=v0H61Dlb 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=Ed2K9V55 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW" width="220" height="186" alt="Polygenic scores for heart disease" title="Polygenic scores for heart disease" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">More diverse datasets lead to better genetic risk prediction for heart disease </span> </a> </div> </article> </div> <div class="field__item"><article about="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=45Sone65 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0" width="220" height="186" alt="Niall Lennon, chief scientific officer and chair of the board of BCL" title="Niall Lennon, chief scientific officer and chair of the board of BCL" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">Q&amp;A: ӳý’s newly renamed clinical lab marks a turning point for the institute’s Genomics Platform</span> </a> </div> </article> </div> </div> </div> </div> </div> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>By analyzing millions of small genetic differences across a person’s genome, researchers can calculate a polygenic risk score to estimate someone’s lifetime odds of developing a certain disease. Over the past decade, scientists have developed these risk scores for dozens of diseases, including heart disease, kidney disease, diabetes, and cancer, with the hope that patients could one day use this information to lower any heightened risk of disease. But determining whether such tests work effectively across all populations, and how they can guide clinical decision-making, has been a challenge.</p> <p>Now, a team of researchers at the ӳý of MIT and Harvard, in collaboration with 10 academic medical centers across the US, has implemented 10 such tests for use in clinical research. In a study published today in <a href="https://www.nature.com/articles/s41591-024-02796-z"><em>Nature Medicine</em></a>, the team outlined how they selected, optimized, and validated the tests for 10 common diseases, including heart disease, breast cancer, and type 2 diabetes. They also calibrated the tests for use in people with non-European ancestries.</p> <p>The scientists worked in collaboration with the national <a href="https://emerge-network.org/">Electronic Medical Records and Genomics (eMERGE) network</a>, which is funded by the National Human Genome Research Institute to study how patients’ genetic data can be integrated with their electronic medical records to improve clinical care and health outcomes. The 10 collaborating medical centers are part of the project and enrolling 25,000 participants for it, while researchers at <a href="https://broadclinicallabs.org/">ӳý Clinical Labs</a>, a subsidiary of the ӳý, carry out the polygenic risk score testing for those participants.</p> <p>“There have been a lot of ongoing conversations and debates about polygenic risk scores and their utility and applicability in the clinical setting,” said <a href="/bios/niall-lennon">Niall Lennon</a>, chief scientific officer of ӳý Clinical Labs, an institute scientist at ӳý, and first author of the new paper. “With this work, we’ve taken the first steps toward showing the potential strength and power of these scores across a diverse population. We hope in the future this kind of information can be used in preventive medicine to help people take actions that lower their risk of disease.”</p> <h2>What’s the score?</h2> <p>Most polygenic risk scores have been developed based on genetic data largely from people of European ancestry, raising questions about whether the scores are applicable to people of other ancestries.</p> <p>To optimize polygenic risk scores for a diversity of people, Lennon and his colleagues first combed the literature looking for polygenic risk scores that had been tested in people from at least two different genetic ancestries. They also searched for scores that indicate a disease risk that patients could reduce with medical treatments, screening, and/or lifestyle changes. &nbsp;</p> <p>“It was important that we weren’t giving people results that they couldn’t do anything about,” said Lennon.</p> <p>The team selected 10 conditions to focus on for polygenic risk scores: atrial fibrillation, breast cancer, chronic kidney disease, coronary heart disease, hypercholesterolemia, prostate cancer, asthma, type 1 diabetes, obesity, and type 2 diabetes.&nbsp;</p> <p>For each condition, the researchers identified the exact spots in the genome that they would analyze to calculate the risk score. They verified that all those spots could be accurately genotyped, by comparing the results of their tests with whole genome sequences from each patient’s blood sample.</p> <p>Finally, the researchers wanted to make polygenic risk scores work across different genetic ancestries. They studied how genetic variants differ across populations by analyzing data from the National Institutes of Health’s All of Us research program, which is collecting health information from one million people from diverse backgrounds across the U.S. The team used that information to create a model to calibrate a person’s polygenic risk score according to that individual’s genetic ancestry.</p> <p>“We can’t fix all biases in the risk scores, but we can make sure that if a person is in a high-risk group for a disease, they’ll get identified as high risk regardless of what their genetic ancestry is,” explained Lennon.</p> <p>With that optimization complete, Lennon’s team at ӳý Clinical Labs ended up with 10 tests that they are now using to calculate risk scores for the 25,000 people enrolled in the eMERGE study. With their eMERGE collaborators, they are also planning detailed follow-up studies to analyze how polygenic risk scores might influence patients’ health care.</p> <p>“Ultimately, the network wants to know what it means for a person to receive information that says they’re at high risk for one of these diseases,” Lennon said.<br> &nbsp;</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro paragraph--view-mode--default"> <div class="field field--name-field-paragraph field--type-entity-reference-revisions field--label-hidden field__items"> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Funding</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>This phase of the eMERGE Network was initiated and funded by the National Human Genome Research Institute.</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Paper cited:</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>Lennon, NJ. et al. <a href="https://www.nature.com/articles/s41591-024-02796-z">Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations</a>. <em>Nature Medicine</em>. Online February 19, 2024. DOI: 10.1038/s41591-024-02796-z</p> </div> </div> </div> </div> </div> </div> </div> </div> </div> </div> <div class="content-section container"> <div class="content-section__main"> <div class="block-node-broad-tags block block-layout-builder block-field-blocknodelong-storyfield-broad-tags"> <div class="block-node-broad-tags__row"> <div class="block-node-broad-tags__title">Tags:</div> <div class="field field--name-field-broad-tags field--type-entity-reference field--label-hidden field__items"> <div class="field__item"><a href="/broad-tags/broad-clinical-labs" hreflang="en">ӳý Clinical Labs</a></div> <div class="field__item"><a href="/broad-tags/using-genomics-predict-disease-risk" hreflang="en">Using genomics to predict disease risk</a></div> </div> </div> </div> </div> </div> Mon, 19 Feb 2024 16:00:28 +0000 Corie Lok 5556476 at A scientist devotes her career to tackling inequity in genomics /news/scientist-devotes-her-career-tackling-inequity-genomics <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> <span class="field field--name-uid field--type-entity-reference field--label-hidden"> <span>By Corie Lok</span> </span> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" class="datetime">February 19, 2024</time> </span> <div class="hero-section container"> <div class="hero-section__row row"> <div class="hero-section__content hero-section__content_left col-6"> <div class="hero-section__breadcrumbs"> <div class="block block-system block-system-breadcrumb-block"> <nav class="breadcrumb" role="navigation" aria-labelledby="system-breadcrumb"> <h2 id="system-breadcrumb" class="visually-hidden">Breadcrumb</h2> <ol> <li> <a href="/">Home</a> </li> <li> <a href="/news">News</a> </li> </ol> </nav> </div> </div> <div class="hero-section__title"> <div class="block block-layout-builder block-field-blocknodelong-storytitle"> <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> </div> </div> <div class="hero-section__description"> <div class="block block-layout-builder block-field-blocknodelong-storybody"> <div class="clearfix text-formatted field field--name-body field--type-text-with-summary field--label-hidden field__item"><p>As part of a nationwide collaboration, ӳý Clinical Labs researchers have optimized 10 polygenic scores for use in clinical research as part of a study on how to implement genetic risk prediction for patients.</p> </div> </div> </div> <div class="hero-section__author"> <div class="block block-layout-builder block-extra-field-blocknodelong-storyextra-field-author-custom"> By Sarah C.P. Williams </div> </div> <div class="hero-section__date"> <div class="block block-layout-builder block-field-blocknodelong-storycreated"> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" title="Monday, February 19, 2024 - 11:00" class="datetime">February 19, 2024</time> </span> </div> </div> </div> <div class="hero-section__right col-6"> <div class="hero-section__image"> <div class="block block-layout-builder block-field-blocknodelong-storyfield-image"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"> <article class="media media--type-image media--view-mode-multiple-content-types-header"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <picture> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1921px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop/public/longstory/PRS_image.png?itok=2jyY3u4P 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="736" height="520"> <source srcset="/files/styles/multiple_ct_header_laptop/public/longstory/PRS_image.png?itok=pkoJbldP 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="641" height="451"> <source srcset="/files/styles/multiple_ct_header_tablet/public/longstory/PRS_image.png?itok=eKNyOfkD 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="706" height="417"> <source srcset="/files/styles/multiple_ct_header_phone/public/longstory/PRS_image.png?itok=drWXPi5h 1x" media="all and (max-width: 539px)" 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class="field__item"><article about="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=v0H61Dlb 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=v0H61Dlb 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=Ed2K9V55 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW" width="220" height="186" alt="Polygenic scores for heart disease" title="Polygenic scores for heart disease" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">More diverse datasets lead to better genetic risk prediction for heart disease </span> </a> </div> </article> </div> <div class="field__item"><article about="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=45Sone65 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0" width="220" height="186" alt="Niall Lennon, chief scientific officer and chair of the board of BCL" title="Niall Lennon, chief scientific officer and chair of the board of BCL" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">Q&amp;A: ӳý’s newly renamed clinical lab marks a turning point for the institute’s Genomics Platform</span> </a> </div> </article> </div> </div> </div> </div> </div> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>By analyzing millions of small genetic differences across a person’s genome, researchers can calculate a polygenic risk score to estimate someone’s lifetime odds of developing a certain disease. Over the past decade, scientists have developed these risk scores for dozens of diseases, including heart disease, kidney disease, diabetes, and cancer, with the hope that patients could one day use this information to lower any heightened risk of disease. But determining whether such tests work effectively across all populations, and how they can guide clinical decision-making, has been a challenge.</p> <p>Now, a team of researchers at the ӳý of MIT and Harvard, in collaboration with 10 academic medical centers across the US, has implemented 10 such tests for use in clinical research. In a study published today in <a href="https://www.nature.com/articles/s41591-024-02796-z"><em>Nature Medicine</em></a>, the team outlined how they selected, optimized, and validated the tests for 10 common diseases, including heart disease, breast cancer, and type 2 diabetes. They also calibrated the tests for use in people with non-European ancestries.</p> <p>The scientists worked in collaboration with the national <a href="https://emerge-network.org/">Electronic Medical Records and Genomics (eMERGE) network</a>, which is funded by the National Human Genome Research Institute to study how patients’ genetic data can be integrated with their electronic medical records to improve clinical care and health outcomes. The 10 collaborating medical centers are part of the project and enrolling 25,000 participants for it, while researchers at <a href="https://broadclinicallabs.org/">ӳý Clinical Labs</a>, a subsidiary of the ӳý, carry out the polygenic risk score testing for those participants.</p> <p>“There have been a lot of ongoing conversations and debates about polygenic risk scores and their utility and applicability in the clinical setting,” said <a href="/bios/niall-lennon">Niall Lennon</a>, chief scientific officer of ӳý Clinical Labs, an institute scientist at ӳý, and first author of the new paper. “With this work, we’ve taken the first steps toward showing the potential strength and power of these scores across a diverse population. We hope in the future this kind of information can be used in preventive medicine to help people take actions that lower their risk of disease.”</p> <h2>What’s the score?</h2> <p>Most polygenic risk scores have been developed based on genetic data largely from people of European ancestry, raising questions about whether the scores are applicable to people of other ancestries.</p> <p>To optimize polygenic risk scores for a diversity of people, Lennon and his colleagues first combed the literature looking for polygenic risk scores that had been tested in people from at least two different genetic ancestries. They also searched for scores that indicate a disease risk that patients could reduce with medical treatments, screening, and/or lifestyle changes. &nbsp;</p> <p>“It was important that we weren’t giving people results that they couldn’t do anything about,” said Lennon.</p> <p>The team selected 10 conditions to focus on for polygenic risk scores: atrial fibrillation, breast cancer, chronic kidney disease, coronary heart disease, hypercholesterolemia, prostate cancer, asthma, type 1 diabetes, obesity, and type 2 diabetes.&nbsp;</p> <p>For each condition, the researchers identified the exact spots in the genome that they would analyze to calculate the risk score. They verified that all those spots could be accurately genotyped, by comparing the results of their tests with whole genome sequences from each patient’s blood sample.</p> <p>Finally, the researchers wanted to make polygenic risk scores work across different genetic ancestries. They studied how genetic variants differ across populations by analyzing data from the National Institutes of Health’s All of Us research program, which is collecting health information from one million people from diverse backgrounds across the U.S. The team used that information to create a model to calibrate a person’s polygenic risk score according to that individual’s genetic ancestry.</p> <p>“We can’t fix all biases in the risk scores, but we can make sure that if a person is in a high-risk group for a disease, they’ll get identified as high risk regardless of what their genetic ancestry is,” explained Lennon.</p> <p>With that optimization complete, Lennon’s team at ӳý Clinical Labs ended up with 10 tests that they are now using to calculate risk scores for the 25,000 people enrolled in the eMERGE study. With their eMERGE collaborators, they are also planning detailed follow-up studies to analyze how polygenic risk scores might influence patients’ health care.</p> <p>“Ultimately, the network wants to know what it means for a person to receive information that says they’re at high risk for one of these diseases,” Lennon said.<br> &nbsp;</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro paragraph--view-mode--default"> <div class="field field--name-field-paragraph field--type-entity-reference-revisions field--label-hidden field__items"> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Funding</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>This phase of the eMERGE Network was initiated and funded by the National Human Genome Research Institute.</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Paper cited:</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>Lennon, NJ. et al. <a href="https://www.nature.com/articles/s41591-024-02796-z">Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations</a>. <em>Nature Medicine</em>. Online February 19, 2024. DOI: 10.1038/s41591-024-02796-z</p> </div> </div> </div> </div> </div> </div> </div> </div> </div> </div> <div class="content-section container"> <div class="content-section__main"> <div class="block-node-broad-tags block block-layout-builder block-field-blocknodelong-storyfield-broad-tags"> <div class="block-node-broad-tags__row"> <div class="block-node-broad-tags__title">Tags:</div> <div class="field field--name-field-broad-tags field--type-entity-reference field--label-hidden field__items"> <div class="field__item"><a href="/broad-tags/broad-clinical-labs" hreflang="en">ӳý Clinical Labs</a></div> <div class="field__item"><a href="/broad-tags/using-genomics-predict-disease-risk" hreflang="en">Using genomics to predict disease risk</a></div> </div> </div> </div> </div> </div> Mon, 10 Jul 2023 15:00:00 +0000 adicorat 1282196 at More diverse datasets lead to better genetic risk prediction for heart disease /news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> <span class="field field--name-uid field--type-entity-reference field--label-hidden"> <span>By Corie Lok</span> </span> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" class="datetime">February 19, 2024</time> </span> <div class="hero-section container"> <div class="hero-section__row row"> <div class="hero-section__content hero-section__content_left col-6"> <div class="hero-section__breadcrumbs"> <div class="block block-system block-system-breadcrumb-block"> <nav class="breadcrumb" role="navigation" aria-labelledby="system-breadcrumb"> <h2 id="system-breadcrumb" class="visually-hidden">Breadcrumb</h2> <ol> <li> <a href="/">Home</a> </li> <li> <a href="/news">News</a> </li> </ol> </nav> </div> </div> <div class="hero-section__title"> <div class="block block-layout-builder block-field-blocknodelong-storytitle"> <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> </div> </div> <div class="hero-section__description"> <div class="block block-layout-builder block-field-blocknodelong-storybody"> <div class="clearfix text-formatted field field--name-body field--type-text-with-summary field--label-hidden field__item"><p>As part of a nationwide collaboration, ӳý Clinical Labs researchers have optimized 10 polygenic scores for use in clinical research as part of a study on how to implement genetic risk prediction for patients.</p> </div> </div> </div> <div class="hero-section__author"> <div class="block block-layout-builder block-extra-field-blocknodelong-storyextra-field-author-custom"> By Sarah C.P. Williams </div> </div> <div class="hero-section__date"> <div class="block block-layout-builder block-field-blocknodelong-storycreated"> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" title="Monday, February 19, 2024 - 11:00" class="datetime">February 19, 2024</time> </span> </div> </div> </div> <div class="hero-section__right col-6"> <div class="hero-section__image"> <div class="block block-layout-builder block-field-blocknodelong-storyfield-image"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"> <article class="media media--type-image media--view-mode-multiple-content-types-header"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <picture> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1921px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop/public/longstory/PRS_image.png?itok=2jyY3u4P 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="736" height="520"> <source srcset="/files/styles/multiple_ct_header_laptop/public/longstory/PRS_image.png?itok=pkoJbldP 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="641" height="451"> <source srcset="/files/styles/multiple_ct_header_tablet/public/longstory/PRS_image.png?itok=eKNyOfkD 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="706" height="417"> <source srcset="/files/styles/multiple_ct_header_phone/public/longstory/PRS_image.png?itok=drWXPi5h 1x" media="all and (max-width: 539px)" 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type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=Ed2K9V55 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW" width="220" height="186" alt="Polygenic scores for heart disease" title="Polygenic scores for heart disease" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">More diverse datasets lead to better genetic risk prediction for heart disease </span> </a> </div> </article> </div> <div class="field__item"><article about="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=45Sone65 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0" width="220" height="186" alt="Niall Lennon, chief scientific officer and chair of the board of BCL" title="Niall Lennon, chief scientific officer and chair of the board of BCL" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">Q&amp;A: ӳý’s newly renamed clinical lab marks a turning point for the institute’s Genomics Platform</span> </a> </div> </article> </div> </div> </div> </div> </div> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>By analyzing millions of small genetic differences across a person’s genome, researchers can calculate a polygenic risk score to estimate someone’s lifetime odds of developing a certain disease. Over the past decade, scientists have developed these risk scores for dozens of diseases, including heart disease, kidney disease, diabetes, and cancer, with the hope that patients could one day use this information to lower any heightened risk of disease. But determining whether such tests work effectively across all populations, and how they can guide clinical decision-making, has been a challenge.</p> <p>Now, a team of researchers at the ӳý of MIT and Harvard, in collaboration with 10 academic medical centers across the US, has implemented 10 such tests for use in clinical research. In a study published today in <a href="https://www.nature.com/articles/s41591-024-02796-z"><em>Nature Medicine</em></a>, the team outlined how they selected, optimized, and validated the tests for 10 common diseases, including heart disease, breast cancer, and type 2 diabetes. They also calibrated the tests for use in people with non-European ancestries.</p> <p>The scientists worked in collaboration with the national <a href="https://emerge-network.org/">Electronic Medical Records and Genomics (eMERGE) network</a>, which is funded by the National Human Genome Research Institute to study how patients’ genetic data can be integrated with their electronic medical records to improve clinical care and health outcomes. The 10 collaborating medical centers are part of the project and enrolling 25,000 participants for it, while researchers at <a href="https://broadclinicallabs.org/">ӳý Clinical Labs</a>, a subsidiary of the ӳý, carry out the polygenic risk score testing for those participants.</p> <p>“There have been a lot of ongoing conversations and debates about polygenic risk scores and their utility and applicability in the clinical setting,” said <a href="/bios/niall-lennon">Niall Lennon</a>, chief scientific officer of ӳý Clinical Labs, an institute scientist at ӳý, and first author of the new paper. “With this work, we’ve taken the first steps toward showing the potential strength and power of these scores across a diverse population. We hope in the future this kind of information can be used in preventive medicine to help people take actions that lower their risk of disease.”</p> <h2>What’s the score?</h2> <p>Most polygenic risk scores have been developed based on genetic data largely from people of European ancestry, raising questions about whether the scores are applicable to people of other ancestries.</p> <p>To optimize polygenic risk scores for a diversity of people, Lennon and his colleagues first combed the literature looking for polygenic risk scores that had been tested in people from at least two different genetic ancestries. They also searched for scores that indicate a disease risk that patients could reduce with medical treatments, screening, and/or lifestyle changes. &nbsp;</p> <p>“It was important that we weren’t giving people results that they couldn’t do anything about,” said Lennon.</p> <p>The team selected 10 conditions to focus on for polygenic risk scores: atrial fibrillation, breast cancer, chronic kidney disease, coronary heart disease, hypercholesterolemia, prostate cancer, asthma, type 1 diabetes, obesity, and type 2 diabetes.&nbsp;</p> <p>For each condition, the researchers identified the exact spots in the genome that they would analyze to calculate the risk score. They verified that all those spots could be accurately genotyped, by comparing the results of their tests with whole genome sequences from each patient’s blood sample.</p> <p>Finally, the researchers wanted to make polygenic risk scores work across different genetic ancestries. They studied how genetic variants differ across populations by analyzing data from the National Institutes of Health’s All of Us research program, which is collecting health information from one million people from diverse backgrounds across the U.S. The team used that information to create a model to calibrate a person’s polygenic risk score according to that individual’s genetic ancestry.</p> <p>“We can’t fix all biases in the risk scores, but we can make sure that if a person is in a high-risk group for a disease, they’ll get identified as high risk regardless of what their genetic ancestry is,” explained Lennon.</p> <p>With that optimization complete, Lennon’s team at ӳý Clinical Labs ended up with 10 tests that they are now using to calculate risk scores for the 25,000 people enrolled in the eMERGE study. With their eMERGE collaborators, they are also planning detailed follow-up studies to analyze how polygenic risk scores might influence patients’ health care.</p> <p>“Ultimately, the network wants to know what it means for a person to receive information that says they’re at high risk for one of these diseases,” Lennon said.<br> &nbsp;</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro paragraph--view-mode--default"> <div class="field field--name-field-paragraph field--type-entity-reference-revisions field--label-hidden field__items"> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Funding</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>This phase of the eMERGE Network was initiated and funded by the National Human Genome Research Institute.</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Paper cited:</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>Lennon, NJ. et al. <a href="https://www.nature.com/articles/s41591-024-02796-z">Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations</a>. <em>Nature Medicine</em>. Online February 19, 2024. DOI: 10.1038/s41591-024-02796-z</p> </div> </div> </div> </div> </div> </div> </div> </div> </div> </div> <div class="content-section container"> <div class="content-section__main"> <div class="block-node-broad-tags block block-layout-builder block-field-blocknodelong-storyfield-broad-tags"> <div class="block-node-broad-tags__row"> <div class="block-node-broad-tags__title">Tags:</div> <div class="field field--name-field-broad-tags field--type-entity-reference field--label-hidden field__items"> <div class="field__item"><a href="/broad-tags/broad-clinical-labs" hreflang="en">ӳý Clinical Labs</a></div> <div class="field__item"><a href="/broad-tags/using-genomics-predict-disease-risk" hreflang="en">Using genomics to predict disease risk</a></div> </div> </div> </div> </div> </div> Thu, 06 Jul 2023 15:00:00 +0000 leah@broadinstitute.org 1282446 at Rare genetic variants can reveal much about disease biology /news/rare-genetic-variants-can-reveal-much-about-disease-biology <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> <span class="field field--name-uid field--type-entity-reference field--label-hidden"> <span>By Corie Lok</span> </span> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" class="datetime">February 19, 2024</time> </span> <div class="hero-section container"> <div class="hero-section__row row"> <div class="hero-section__content hero-section__content_left col-6"> <div class="hero-section__breadcrumbs"> <div class="block block-system block-system-breadcrumb-block"> <nav class="breadcrumb" role="navigation" aria-labelledby="system-breadcrumb"> <h2 id="system-breadcrumb" class="visually-hidden">Breadcrumb</h2> <ol> <li> <a href="/">Home</a> </li> <li> <a href="/news">News</a> </li> </ol> </nav> </div> </div> <div class="hero-section__title"> <div class="block block-layout-builder block-field-blocknodelong-storytitle"> <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> </div> </div> <div class="hero-section__description"> <div class="block block-layout-builder block-field-blocknodelong-storybody"> <div class="clearfix text-formatted field field--name-body field--type-text-with-summary field--label-hidden field__item"><p>As part of a nationwide collaboration, ӳý Clinical Labs researchers have optimized 10 polygenic scores for use in clinical research as part of a study on how to implement genetic risk prediction for patients.</p> </div> </div> </div> <div class="hero-section__author"> <div class="block block-layout-builder block-extra-field-blocknodelong-storyextra-field-author-custom"> By Sarah C.P. Williams </div> </div> <div class="hero-section__date"> <div class="block block-layout-builder block-field-blocknodelong-storycreated"> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" title="Monday, February 19, 2024 - 11:00" class="datetime">February 19, 2024</time> </span> </div> </div> </div> <div class="hero-section__right col-6"> <div class="hero-section__image"> <div class="block block-layout-builder block-field-blocknodelong-storyfield-image"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"> <article class="media media--type-image media--view-mode-multiple-content-types-header"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <picture> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1921px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop/public/longstory/PRS_image.png?itok=2jyY3u4P 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="736" height="520"> <source srcset="/files/styles/multiple_ct_header_laptop/public/longstory/PRS_image.png?itok=pkoJbldP 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="641" height="451"> <source srcset="/files/styles/multiple_ct_header_tablet/public/longstory/PRS_image.png?itok=eKNyOfkD 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="706" height="417"> <source srcset="/files/styles/multiple_ct_header_phone/public/longstory/PRS_image.png?itok=drWXPi5h 1x" media="all and (max-width: 539px)" 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class="field__item"><article about="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=v0H61Dlb 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=v0H61Dlb 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" 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(max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW" width="220" height="186" alt="Polygenic scores for heart disease" title="Polygenic scores for heart disease" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">More diverse datasets lead to better genetic risk prediction for heart disease </span> </a> </div> </article> </div> <div class="field__item"><article about="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=45Sone65 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0" width="220" height="186" alt="Niall Lennon, chief scientific officer and chair of the board of BCL" title="Niall Lennon, chief scientific officer and chair of the board of BCL" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">Q&amp;A: ӳý’s newly renamed clinical lab marks a turning point for the institute’s Genomics Platform</span> </a> </div> </article> </div> </div> </div> </div> </div> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>By analyzing millions of small genetic differences across a person’s genome, researchers can calculate a polygenic risk score to estimate someone’s lifetime odds of developing a certain disease. Over the past decade, scientists have developed these risk scores for dozens of diseases, including heart disease, kidney disease, diabetes, and cancer, with the hope that patients could one day use this information to lower any heightened risk of disease. But determining whether such tests work effectively across all populations, and how they can guide clinical decision-making, has been a challenge.</p> <p>Now, a team of researchers at the ӳý of MIT and Harvard, in collaboration with 10 academic medical centers across the US, has implemented 10 such tests for use in clinical research. In a study published today in <a href="https://www.nature.com/articles/s41591-024-02796-z"><em>Nature Medicine</em></a>, the team outlined how they selected, optimized, and validated the tests for 10 common diseases, including heart disease, breast cancer, and type 2 diabetes. They also calibrated the tests for use in people with non-European ancestries.</p> <p>The scientists worked in collaboration with the national <a href="https://emerge-network.org/">Electronic Medical Records and Genomics (eMERGE) network</a>, which is funded by the National Human Genome Research Institute to study how patients’ genetic data can be integrated with their electronic medical records to improve clinical care and health outcomes. The 10 collaborating medical centers are part of the project and enrolling 25,000 participants for it, while researchers at <a href="https://broadclinicallabs.org/">ӳý Clinical Labs</a>, a subsidiary of the ӳý, carry out the polygenic risk score testing for those participants.</p> <p>“There have been a lot of ongoing conversations and debates about polygenic risk scores and their utility and applicability in the clinical setting,” said <a href="/bios/niall-lennon">Niall Lennon</a>, chief scientific officer of ӳý Clinical Labs, an institute scientist at ӳý, and first author of the new paper. “With this work, we’ve taken the first steps toward showing the potential strength and power of these scores across a diverse population. We hope in the future this kind of information can be used in preventive medicine to help people take actions that lower their risk of disease.”</p> <h2>What’s the score?</h2> <p>Most polygenic risk scores have been developed based on genetic data largely from people of European ancestry, raising questions about whether the scores are applicable to people of other ancestries.</p> <p>To optimize polygenic risk scores for a diversity of people, Lennon and his colleagues first combed the literature looking for polygenic risk scores that had been tested in people from at least two different genetic ancestries. They also searched for scores that indicate a disease risk that patients could reduce with medical treatments, screening, and/or lifestyle changes. &nbsp;</p> <p>“It was important that we weren’t giving people results that they couldn’t do anything about,” said Lennon.</p> <p>The team selected 10 conditions to focus on for polygenic risk scores: atrial fibrillation, breast cancer, chronic kidney disease, coronary heart disease, hypercholesterolemia, prostate cancer, asthma, type 1 diabetes, obesity, and type 2 diabetes.&nbsp;</p> <p>For each condition, the researchers identified the exact spots in the genome that they would analyze to calculate the risk score. They verified that all those spots could be accurately genotyped, by comparing the results of their tests with whole genome sequences from each patient’s blood sample.</p> <p>Finally, the researchers wanted to make polygenic risk scores work across different genetic ancestries. They studied how genetic variants differ across populations by analyzing data from the National Institutes of Health’s All of Us research program, which is collecting health information from one million people from diverse backgrounds across the U.S. The team used that information to create a model to calibrate a person’s polygenic risk score according to that individual’s genetic ancestry.</p> <p>“We can’t fix all biases in the risk scores, but we can make sure that if a person is in a high-risk group for a disease, they’ll get identified as high risk regardless of what their genetic ancestry is,” explained Lennon.</p> <p>With that optimization complete, Lennon’s team at ӳý Clinical Labs ended up with 10 tests that they are now using to calculate risk scores for the 25,000 people enrolled in the eMERGE study. With their eMERGE collaborators, they are also planning detailed follow-up studies to analyze how polygenic risk scores might influence patients’ health care.</p> <p>“Ultimately, the network wants to know what it means for a person to receive information that says they’re at high risk for one of these diseases,” Lennon said.<br> &nbsp;</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro paragraph--view-mode--default"> <div class="field field--name-field-paragraph field--type-entity-reference-revisions field--label-hidden field__items"> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Funding</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>This phase of the eMERGE Network was initiated and funded by the National Human Genome Research Institute.</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Paper cited:</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>Lennon, NJ. et al. <a href="https://www.nature.com/articles/s41591-024-02796-z">Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations</a>. <em>Nature Medicine</em>. Online February 19, 2024. DOI: 10.1038/s41591-024-02796-z</p> </div> </div> </div> </div> </div> </div> </div> </div> </div> </div> <div class="content-section container"> <div class="content-section__main"> <div class="block-node-broad-tags block block-layout-builder block-field-blocknodelong-storyfield-broad-tags"> <div class="block-node-broad-tags__row"> <div class="block-node-broad-tags__title">Tags:</div> <div class="field field--name-field-broad-tags field--type-entity-reference field--label-hidden field__items"> <div class="field__item"><a href="/broad-tags/broad-clinical-labs" hreflang="en">ӳý Clinical Labs</a></div> <div class="field__item"><a href="/broad-tags/using-genomics-predict-disease-risk" hreflang="en">Using genomics to predict disease risk</a></div> </div> </div> </div> </div> </div> Wed, 08 Feb 2023 22:39:07 +0000 tulrich@broadinstitute.org 1281666 at ӳý Discovery Center in Cambridge opens to the public this October /news/broad-discovery-center-cambridge-opens-public-october <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> <span class="field field--name-uid field--type-entity-reference field--label-hidden"> <span>By Corie Lok</span> </span> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" class="datetime">February 19, 2024</time> </span> <div class="hero-section container"> <div class="hero-section__row row"> <div class="hero-section__content hero-section__content_left col-6"> <div class="hero-section__breadcrumbs"> <div class="block block-system block-system-breadcrumb-block"> <nav class="breadcrumb" role="navigation" aria-labelledby="system-breadcrumb"> <h2 id="system-breadcrumb" class="visually-hidden">Breadcrumb</h2> <ol> <li> <a href="/">Home</a> </li> <li> <a href="/news">News</a> </li> </ol> </nav> </div> </div> <div class="hero-section__title"> <div class="block block-layout-builder block-field-blocknodelong-storytitle"> <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> </div> </div> <div class="hero-section__description"> <div class="block block-layout-builder block-field-blocknodelong-storybody"> <div class="clearfix text-formatted field field--name-body field--type-text-with-summary field--label-hidden field__item"><p>As part of a nationwide collaboration, ӳý Clinical Labs researchers have optimized 10 polygenic scores for use in clinical research as part of a study on how to implement genetic risk prediction for patients.</p> </div> </div> </div> <div class="hero-section__author"> <div class="block block-layout-builder block-extra-field-blocknodelong-storyextra-field-author-custom"> By Sarah C.P. Williams </div> </div> <div class="hero-section__date"> <div class="block block-layout-builder block-field-blocknodelong-storycreated"> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" title="Monday, February 19, 2024 - 11:00" class="datetime">February 19, 2024</time> </span> </div> </div> </div> <div class="hero-section__right col-6"> <div class="hero-section__image"> <div class="block block-layout-builder block-field-blocknodelong-storyfield-image"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"> <article class="media media--type-image media--view-mode-multiple-content-types-header"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <picture> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1921px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop/public/longstory/PRS_image.png?itok=2jyY3u4P 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="736" height="520"> <source srcset="/files/styles/multiple_ct_header_laptop/public/longstory/PRS_image.png?itok=pkoJbldP 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="641" height="451"> <source srcset="/files/styles/multiple_ct_header_tablet/public/longstory/PRS_image.png?itok=eKNyOfkD 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="706" height="417"> <source srcset="/files/styles/multiple_ct_header_phone/public/longstory/PRS_image.png?itok=drWXPi5h 1x" media="all and (max-width: 539px)" 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class="field__item"><article about="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=v0H61Dlb 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=v0H61Dlb 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=Ed2K9V55 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW" width="220" height="186" alt="Polygenic scores for heart disease" title="Polygenic scores for heart disease" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">More diverse datasets lead to better genetic risk prediction for heart disease </span> </a> </div> </article> </div> <div class="field__item"><article about="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=45Sone65 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0" width="220" height="186" alt="Niall Lennon, chief scientific officer and chair of the board of BCL" title="Niall Lennon, chief scientific officer and chair of the board of BCL" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">Q&amp;A: ӳý’s newly renamed clinical lab marks a turning point for the institute’s Genomics Platform</span> </a> </div> </article> </div> </div> </div> </div> </div> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>By analyzing millions of small genetic differences across a person’s genome, researchers can calculate a polygenic risk score to estimate someone’s lifetime odds of developing a certain disease. Over the past decade, scientists have developed these risk scores for dozens of diseases, including heart disease, kidney disease, diabetes, and cancer, with the hope that patients could one day use this information to lower any heightened risk of disease. But determining whether such tests work effectively across all populations, and how they can guide clinical decision-making, has been a challenge.</p> <p>Now, a team of researchers at the ӳý of MIT and Harvard, in collaboration with 10 academic medical centers across the US, has implemented 10 such tests for use in clinical research. In a study published today in <a href="https://www.nature.com/articles/s41591-024-02796-z"><em>Nature Medicine</em></a>, the team outlined how they selected, optimized, and validated the tests for 10 common diseases, including heart disease, breast cancer, and type 2 diabetes. They also calibrated the tests for use in people with non-European ancestries.</p> <p>The scientists worked in collaboration with the national <a href="https://emerge-network.org/">Electronic Medical Records and Genomics (eMERGE) network</a>, which is funded by the National Human Genome Research Institute to study how patients’ genetic data can be integrated with their electronic medical records to improve clinical care and health outcomes. The 10 collaborating medical centers are part of the project and enrolling 25,000 participants for it, while researchers at <a href="https://broadclinicallabs.org/">ӳý Clinical Labs</a>, a subsidiary of the ӳý, carry out the polygenic risk score testing for those participants.</p> <p>“There have been a lot of ongoing conversations and debates about polygenic risk scores and their utility and applicability in the clinical setting,” said <a href="/bios/niall-lennon">Niall Lennon</a>, chief scientific officer of ӳý Clinical Labs, an institute scientist at ӳý, and first author of the new paper. “With this work, we’ve taken the first steps toward showing the potential strength and power of these scores across a diverse population. We hope in the future this kind of information can be used in preventive medicine to help people take actions that lower their risk of disease.”</p> <h2>What’s the score?</h2> <p>Most polygenic risk scores have been developed based on genetic data largely from people of European ancestry, raising questions about whether the scores are applicable to people of other ancestries.</p> <p>To optimize polygenic risk scores for a diversity of people, Lennon and his colleagues first combed the literature looking for polygenic risk scores that had been tested in people from at least two different genetic ancestries. They also searched for scores that indicate a disease risk that patients could reduce with medical treatments, screening, and/or lifestyle changes. &nbsp;</p> <p>“It was important that we weren’t giving people results that they couldn’t do anything about,” said Lennon.</p> <p>The team selected 10 conditions to focus on for polygenic risk scores: atrial fibrillation, breast cancer, chronic kidney disease, coronary heart disease, hypercholesterolemia, prostate cancer, asthma, type 1 diabetes, obesity, and type 2 diabetes.&nbsp;</p> <p>For each condition, the researchers identified the exact spots in the genome that they would analyze to calculate the risk score. They verified that all those spots could be accurately genotyped, by comparing the results of their tests with whole genome sequences from each patient’s blood sample.</p> <p>Finally, the researchers wanted to make polygenic risk scores work across different genetic ancestries. They studied how genetic variants differ across populations by analyzing data from the National Institutes of Health’s All of Us research program, which is collecting health information from one million people from diverse backgrounds across the U.S. The team used that information to create a model to calibrate a person’s polygenic risk score according to that individual’s genetic ancestry.</p> <p>“We can’t fix all biases in the risk scores, but we can make sure that if a person is in a high-risk group for a disease, they’ll get identified as high risk regardless of what their genetic ancestry is,” explained Lennon.</p> <p>With that optimization complete, Lennon’s team at ӳý Clinical Labs ended up with 10 tests that they are now using to calculate risk scores for the 25,000 people enrolled in the eMERGE study. With their eMERGE collaborators, they are also planning detailed follow-up studies to analyze how polygenic risk scores might influence patients’ health care.</p> <p>“Ultimately, the network wants to know what it means for a person to receive information that says they’re at high risk for one of these diseases,” Lennon said.<br> &nbsp;</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro paragraph--view-mode--default"> <div class="field field--name-field-paragraph field--type-entity-reference-revisions field--label-hidden field__items"> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Funding</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>This phase of the eMERGE Network was initiated and funded by the National Human Genome Research Institute.</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Paper cited:</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>Lennon, NJ. et al. <a href="https://www.nature.com/articles/s41591-024-02796-z">Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations</a>. <em>Nature Medicine</em>. Online February 19, 2024. DOI: 10.1038/s41591-024-02796-z</p> </div> </div> </div> </div> </div> </div> </div> </div> </div> </div> <div class="content-section container"> <div class="content-section__main"> <div class="block-node-broad-tags block block-layout-builder block-field-blocknodelong-storyfield-broad-tags"> <div class="block-node-broad-tags__row"> <div class="block-node-broad-tags__title">Tags:</div> <div class="field field--name-field-broad-tags field--type-entity-reference field--label-hidden field__items"> <div class="field__item"><a href="/broad-tags/broad-clinical-labs" hreflang="en">ӳý Clinical Labs</a></div> <div class="field__item"><a href="/broad-tags/using-genomics-predict-disease-risk" hreflang="en">Using genomics to predict disease risk</a></div> </div> </div> </div> </div> </div> Mon, 19 Sep 2022 14:53:09 +0000 kzusi@broadinstitute.org 1195701 at A tool for more accurate disease risk prediction across diverse populations /news/tool-more-accurate-disease-risk-prediction-across-diverse-populations <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> <span class="field field--name-uid field--type-entity-reference field--label-hidden"> <span>By Corie Lok</span> </span> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" class="datetime">February 19, 2024</time> </span> <div class="hero-section container"> <div class="hero-section__row row"> <div class="hero-section__content hero-section__content_left col-6"> <div class="hero-section__breadcrumbs"> <div class="block block-system block-system-breadcrumb-block"> <nav class="breadcrumb" role="navigation" aria-labelledby="system-breadcrumb"> <h2 id="system-breadcrumb" class="visually-hidden">Breadcrumb</h2> <ol> <li> <a href="/">Home</a> </li> <li> <a href="/news">News</a> </li> </ol> </nav> </div> </div> <div class="hero-section__title"> <div class="block block-layout-builder block-field-blocknodelong-storytitle"> <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> </div> </div> <div class="hero-section__description"> <div class="block block-layout-builder block-field-blocknodelong-storybody"> <div class="clearfix text-formatted field field--name-body field--type-text-with-summary field--label-hidden field__item"><p>As part of a nationwide collaboration, ӳý Clinical Labs researchers have optimized 10 polygenic scores for use in clinical research as part of a study on how to implement genetic risk prediction for patients.</p> </div> </div> </div> <div class="hero-section__author"> <div class="block block-layout-builder block-extra-field-blocknodelong-storyextra-field-author-custom"> By Sarah C.P. Williams </div> </div> <div class="hero-section__date"> <div class="block block-layout-builder block-field-blocknodelong-storycreated"> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" title="Monday, February 19, 2024 - 11:00" class="datetime">February 19, 2024</time> </span> </div> </div> </div> <div class="hero-section__right col-6"> <div class="hero-section__image"> <div class="block block-layout-builder block-field-blocknodelong-storyfield-image"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"> <article class="media media--type-image media--view-mode-multiple-content-types-header"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <picture> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1921px)" type="image/png" 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class="field__item"><article about="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=v0H61Dlb 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=v0H61Dlb 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=Ed2K9V55 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW" width="220" height="186" alt="Polygenic scores for heart disease" title="Polygenic scores for heart disease" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">More diverse datasets lead to better genetic risk prediction for heart disease </span> </a> </div> </article> </div> <div class="field__item"><article about="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=45Sone65 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0" width="220" height="186" alt="Niall Lennon, chief scientific officer and chair of the board of BCL" title="Niall Lennon, chief scientific officer and chair of the board of BCL" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">Q&amp;A: ӳý’s newly renamed clinical lab marks a turning point for the institute’s Genomics Platform</span> </a> </div> </article> </div> </div> </div> </div> </div> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>By analyzing millions of small genetic differences across a person’s genome, researchers can calculate a polygenic risk score to estimate someone’s lifetime odds of developing a certain disease. Over the past decade, scientists have developed these risk scores for dozens of diseases, including heart disease, kidney disease, diabetes, and cancer, with the hope that patients could one day use this information to lower any heightened risk of disease. But determining whether such tests work effectively across all populations, and how they can guide clinical decision-making, has been a challenge.</p> <p>Now, a team of researchers at the ӳý of MIT and Harvard, in collaboration with 10 academic medical centers across the US, has implemented 10 such tests for use in clinical research. In a study published today in <a href="https://www.nature.com/articles/s41591-024-02796-z"><em>Nature Medicine</em></a>, the team outlined how they selected, optimized, and validated the tests for 10 common diseases, including heart disease, breast cancer, and type 2 diabetes. They also calibrated the tests for use in people with non-European ancestries.</p> <p>The scientists worked in collaboration with the national <a href="https://emerge-network.org/">Electronic Medical Records and Genomics (eMERGE) network</a>, which is funded by the National Human Genome Research Institute to study how patients’ genetic data can be integrated with their electronic medical records to improve clinical care and health outcomes. The 10 collaborating medical centers are part of the project and enrolling 25,000 participants for it, while researchers at <a href="https://broadclinicallabs.org/">ӳý Clinical Labs</a>, a subsidiary of the ӳý, carry out the polygenic risk score testing for those participants.</p> <p>“There have been a lot of ongoing conversations and debates about polygenic risk scores and their utility and applicability in the clinical setting,” said <a href="/bios/niall-lennon">Niall Lennon</a>, chief scientific officer of ӳý Clinical Labs, an institute scientist at ӳý, and first author of the new paper. “With this work, we’ve taken the first steps toward showing the potential strength and power of these scores across a diverse population. We hope in the future this kind of information can be used in preventive medicine to help people take actions that lower their risk of disease.”</p> <h2>What’s the score?</h2> <p>Most polygenic risk scores have been developed based on genetic data largely from people of European ancestry, raising questions about whether the scores are applicable to people of other ancestries.</p> <p>To optimize polygenic risk scores for a diversity of people, Lennon and his colleagues first combed the literature looking for polygenic risk scores that had been tested in people from at least two different genetic ancestries. They also searched for scores that indicate a disease risk that patients could reduce with medical treatments, screening, and/or lifestyle changes. &nbsp;</p> <p>“It was important that we weren’t giving people results that they couldn’t do anything about,” said Lennon.</p> <p>The team selected 10 conditions to focus on for polygenic risk scores: atrial fibrillation, breast cancer, chronic kidney disease, coronary heart disease, hypercholesterolemia, prostate cancer, asthma, type 1 diabetes, obesity, and type 2 diabetes.&nbsp;</p> <p>For each condition, the researchers identified the exact spots in the genome that they would analyze to calculate the risk score. They verified that all those spots could be accurately genotyped, by comparing the results of their tests with whole genome sequences from each patient’s blood sample.</p> <p>Finally, the researchers wanted to make polygenic risk scores work across different genetic ancestries. They studied how genetic variants differ across populations by analyzing data from the National Institutes of Health’s All of Us research program, which is collecting health information from one million people from diverse backgrounds across the U.S. The team used that information to create a model to calibrate a person’s polygenic risk score according to that individual’s genetic ancestry.</p> <p>“We can’t fix all biases in the risk scores, but we can make sure that if a person is in a high-risk group for a disease, they’ll get identified as high risk regardless of what their genetic ancestry is,” explained Lennon.</p> <p>With that optimization complete, Lennon’s team at ӳý Clinical Labs ended up with 10 tests that they are now using to calculate risk scores for the 25,000 people enrolled in the eMERGE study. With their eMERGE collaborators, they are also planning detailed follow-up studies to analyze how polygenic risk scores might influence patients’ health care.</p> <p>“Ultimately, the network wants to know what it means for a person to receive information that says they’re at high risk for one of these diseases,” Lennon said.<br> &nbsp;</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro paragraph--view-mode--default"> <div class="field field--name-field-paragraph field--type-entity-reference-revisions field--label-hidden field__items"> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Funding</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>This phase of the eMERGE Network was initiated and funded by the National Human Genome Research Institute.</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Paper cited:</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>Lennon, NJ. et al. <a href="https://www.nature.com/articles/s41591-024-02796-z">Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations</a>. <em>Nature Medicine</em>. Online February 19, 2024. DOI: 10.1038/s41591-024-02796-z</p> </div> </div> </div> </div> </div> </div> </div> </div> </div> </div> <div class="content-section container"> <div class="content-section__main"> <div class="block-node-broad-tags block block-layout-builder block-field-blocknodelong-storyfield-broad-tags"> <div class="block-node-broad-tags__row"> <div class="block-node-broad-tags__title">Tags:</div> <div class="field field--name-field-broad-tags field--type-entity-reference field--label-hidden field__items"> <div class="field__item"><a href="/broad-tags/broad-clinical-labs" hreflang="en">ӳý Clinical Labs</a></div> <div class="field__item"><a href="/broad-tags/using-genomics-predict-disease-risk" hreflang="en">Using genomics to predict disease risk</a></div> </div> </div> </div> </div> </div> Thu, 05 May 2022 18:00:00 +0000 tulrich@broadinstitute.org 1131901 at New genetic test for heart attack risk launched for patients at Mass General /news/new-genetic-test-heart-attack-risk-launched-patients-mass-general <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> <span class="field field--name-uid field--type-entity-reference field--label-hidden"> <span>By Corie Lok</span> </span> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" class="datetime">February 19, 2024</time> </span> <div class="hero-section container"> <div class="hero-section__row row"> <div class="hero-section__content hero-section__content_left col-6"> <div class="hero-section__breadcrumbs"> <div class="block block-system block-system-breadcrumb-block"> <nav class="breadcrumb" role="navigation" aria-labelledby="system-breadcrumb"> <h2 id="system-breadcrumb" class="visually-hidden">Breadcrumb</h2> <ol> <li> <a href="/">Home</a> </li> <li> <a href="/news">News</a> </li> </ol> </nav> </div> </div> <div class="hero-section__title"> <div class="block block-layout-builder block-field-blocknodelong-storytitle"> <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> </div> </div> <div class="hero-section__description"> <div class="block block-layout-builder block-field-blocknodelong-storybody"> <div class="clearfix text-formatted field field--name-body field--type-text-with-summary field--label-hidden field__item"><p>As part of a nationwide collaboration, ӳý Clinical Labs researchers have optimized 10 polygenic scores for use in clinical research as part of a study on how to implement genetic risk prediction for patients.</p> </div> </div> </div> <div class="hero-section__author"> <div class="block block-layout-builder block-extra-field-blocknodelong-storyextra-field-author-custom"> By Sarah C.P. Williams </div> </div> <div class="hero-section__date"> <div class="block block-layout-builder block-field-blocknodelong-storycreated"> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" title="Monday, February 19, 2024 - 11:00" class="datetime">February 19, 2024</time> </span> </div> </div> </div> <div class="hero-section__right col-6"> <div class="hero-section__image"> <div class="block block-layout-builder block-field-blocknodelong-storyfield-image"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"> <article class="media media--type-image media--view-mode-multiple-content-types-header"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <picture> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1921px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop/public/longstory/PRS_image.png?itok=2jyY3u4P 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="736" height="520"> <source srcset="/files/styles/multiple_ct_header_laptop/public/longstory/PRS_image.png?itok=pkoJbldP 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="641" height="451"> <source srcset="/files/styles/multiple_ct_header_tablet/public/longstory/PRS_image.png?itok=eKNyOfkD 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="706" height="417"> <source srcset="/files/styles/multiple_ct_header_phone/public/longstory/PRS_image.png?itok=drWXPi5h 1x" media="all and (max-width: 539px)" 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class="field__item"><article about="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=v0H61Dlb 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=v0H61Dlb 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=Ed2K9V55 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW" width="220" height="186" alt="Polygenic scores for heart disease" title="Polygenic scores for heart disease" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">More diverse datasets lead to better genetic risk prediction for heart disease </span> </a> </div> </article> </div> <div class="field__item"><article about="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=45Sone65 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0" width="220" height="186" alt="Niall Lennon, chief scientific officer and chair of the board of BCL" title="Niall Lennon, chief scientific officer and chair of the board of BCL" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">Q&amp;A: ӳý’s newly renamed clinical lab marks a turning point for the institute’s Genomics Platform</span> </a> </div> </article> </div> </div> </div> </div> </div> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>By analyzing millions of small genetic differences across a person’s genome, researchers can calculate a polygenic risk score to estimate someone’s lifetime odds of developing a certain disease. Over the past decade, scientists have developed these risk scores for dozens of diseases, including heart disease, kidney disease, diabetes, and cancer, with the hope that patients could one day use this information to lower any heightened risk of disease. But determining whether such tests work effectively across all populations, and how they can guide clinical decision-making, has been a challenge.</p> <p>Now, a team of researchers at the ӳý of MIT and Harvard, in collaboration with 10 academic medical centers across the US, has implemented 10 such tests for use in clinical research. In a study published today in <a href="https://www.nature.com/articles/s41591-024-02796-z"><em>Nature Medicine</em></a>, the team outlined how they selected, optimized, and validated the tests for 10 common diseases, including heart disease, breast cancer, and type 2 diabetes. They also calibrated the tests for use in people with non-European ancestries.</p> <p>The scientists worked in collaboration with the national <a href="https://emerge-network.org/">Electronic Medical Records and Genomics (eMERGE) network</a>, which is funded by the National Human Genome Research Institute to study how patients’ genetic data can be integrated with their electronic medical records to improve clinical care and health outcomes. The 10 collaborating medical centers are part of the project and enrolling 25,000 participants for it, while researchers at <a href="https://broadclinicallabs.org/">ӳý Clinical Labs</a>, a subsidiary of the ӳý, carry out the polygenic risk score testing for those participants.</p> <p>“There have been a lot of ongoing conversations and debates about polygenic risk scores and their utility and applicability in the clinical setting,” said <a href="/bios/niall-lennon">Niall Lennon</a>, chief scientific officer of ӳý Clinical Labs, an institute scientist at ӳý, and first author of the new paper. “With this work, we’ve taken the first steps toward showing the potential strength and power of these scores across a diverse population. We hope in the future this kind of information can be used in preventive medicine to help people take actions that lower their risk of disease.”</p> <h2>What’s the score?</h2> <p>Most polygenic risk scores have been developed based on genetic data largely from people of European ancestry, raising questions about whether the scores are applicable to people of other ancestries.</p> <p>To optimize polygenic risk scores for a diversity of people, Lennon and his colleagues first combed the literature looking for polygenic risk scores that had been tested in people from at least two different genetic ancestries. They also searched for scores that indicate a disease risk that patients could reduce with medical treatments, screening, and/or lifestyle changes. &nbsp;</p> <p>“It was important that we weren’t giving people results that they couldn’t do anything about,” said Lennon.</p> <p>The team selected 10 conditions to focus on for polygenic risk scores: atrial fibrillation, breast cancer, chronic kidney disease, coronary heart disease, hypercholesterolemia, prostate cancer, asthma, type 1 diabetes, obesity, and type 2 diabetes.&nbsp;</p> <p>For each condition, the researchers identified the exact spots in the genome that they would analyze to calculate the risk score. They verified that all those spots could be accurately genotyped, by comparing the results of their tests with whole genome sequences from each patient’s blood sample.</p> <p>Finally, the researchers wanted to make polygenic risk scores work across different genetic ancestries. They studied how genetic variants differ across populations by analyzing data from the National Institutes of Health’s All of Us research program, which is collecting health information from one million people from diverse backgrounds across the U.S. The team used that information to create a model to calibrate a person’s polygenic risk score according to that individual’s genetic ancestry.</p> <p>“We can’t fix all biases in the risk scores, but we can make sure that if a person is in a high-risk group for a disease, they’ll get identified as high risk regardless of what their genetic ancestry is,” explained Lennon.</p> <p>With that optimization complete, Lennon’s team at ӳý Clinical Labs ended up with 10 tests that they are now using to calculate risk scores for the 25,000 people enrolled in the eMERGE study. With their eMERGE collaborators, they are also planning detailed follow-up studies to analyze how polygenic risk scores might influence patients’ health care.</p> <p>“Ultimately, the network wants to know what it means for a person to receive information that says they’re at high risk for one of these diseases,” Lennon said.<br> &nbsp;</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro paragraph--view-mode--default"> <div class="field field--name-field-paragraph field--type-entity-reference-revisions field--label-hidden field__items"> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Funding</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>This phase of the eMERGE Network was initiated and funded by the National Human Genome Research Institute.</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Paper cited:</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>Lennon, NJ. et al. <a href="https://www.nature.com/articles/s41591-024-02796-z">Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations</a>. <em>Nature Medicine</em>. Online February 19, 2024. DOI: 10.1038/s41591-024-02796-z</p> </div> </div> </div> </div> </div> </div> </div> </div> </div> </div> <div class="content-section container"> <div class="content-section__main"> <div class="block-node-broad-tags block block-layout-builder block-field-blocknodelong-storyfield-broad-tags"> <div class="block-node-broad-tags__row"> <div class="block-node-broad-tags__title">Tags:</div> <div class="field field--name-field-broad-tags field--type-entity-reference field--label-hidden field__items"> <div class="field__item"><a href="/broad-tags/broad-clinical-labs" hreflang="en">ӳý Clinical Labs</a></div> <div class="field__item"><a href="/broad-tags/using-genomics-predict-disease-risk" hreflang="en">Using genomics to predict disease risk</a></div> </div> </div> </div> </div> </div> Wed, 27 Jan 2021 18:29:13 +0000 AnnaFiorentinoWriter 742806 at A Schizophrenia Study in Africa is Boosting Equity in Global Genetics Research /schizophrenia-study-africa-boosting-equity-global-genetics-research <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> <span class="field field--name-uid field--type-entity-reference field--label-hidden"> <span>By Corie Lok</span> </span> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" class="datetime">February 19, 2024</time> </span> <div class="hero-section container"> <div class="hero-section__row row"> <div class="hero-section__content hero-section__content_left col-6"> <div class="hero-section__breadcrumbs"> <div class="block block-system block-system-breadcrumb-block"> <nav class="breadcrumb" role="navigation" aria-labelledby="system-breadcrumb"> <h2 id="system-breadcrumb" class="visually-hidden">Breadcrumb</h2> <ol> <li> <a href="/">Home</a> </li> <li> <a href="/news">News</a> </li> </ol> </nav> </div> </div> <div class="hero-section__title"> <div class="block block-layout-builder block-field-blocknodelong-storytitle"> <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> </div> </div> <div class="hero-section__description"> <div class="block block-layout-builder block-field-blocknodelong-storybody"> <div class="clearfix text-formatted field field--name-body field--type-text-with-summary field--label-hidden field__item"><p>As part of a nationwide collaboration, ӳý Clinical Labs researchers have optimized 10 polygenic scores for use in clinical research as part of a study on how to implement genetic risk prediction for patients.</p> </div> </div> </div> <div class="hero-section__author"> <div class="block block-layout-builder block-extra-field-blocknodelong-storyextra-field-author-custom"> By Sarah C.P. Williams </div> </div> <div class="hero-section__date"> <div class="block block-layout-builder block-field-blocknodelong-storycreated"> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" title="Monday, February 19, 2024 - 11:00" class="datetime">February 19, 2024</time> </span> </div> </div> </div> <div class="hero-section__right col-6"> <div class="hero-section__image"> <div class="block block-layout-builder block-field-blocknodelong-storyfield-image"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"> <article class="media media--type-image media--view-mode-multiple-content-types-header"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <picture> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1921px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop/public/longstory/PRS_image.png?itok=2jyY3u4P 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="736" height="520"> <source srcset="/files/styles/multiple_ct_header_laptop/public/longstory/PRS_image.png?itok=pkoJbldP 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="641" height="451"> <source srcset="/files/styles/multiple_ct_header_tablet/public/longstory/PRS_image.png?itok=eKNyOfkD 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="706" height="417"> <source srcset="/files/styles/multiple_ct_header_phone/public/longstory/PRS_image.png?itok=drWXPi5h 1x" media="all and (max-width: 539px)" 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type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=Ed2K9V55 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW" width="220" height="186" alt="Polygenic scores for heart disease" title="Polygenic scores for heart disease" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">More diverse datasets lead to better genetic risk prediction for heart disease </span> </a> </div> </article> </div> <div class="field__item"><article about="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=45Sone65 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0" width="220" height="186" alt="Niall Lennon, chief scientific officer and chair of the board of BCL" title="Niall Lennon, chief scientific officer and chair of the board of BCL" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">Q&amp;A: ӳý’s newly renamed clinical lab marks a turning point for the institute’s Genomics Platform</span> </a> </div> </article> </div> </div> </div> </div> </div> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>By analyzing millions of small genetic differences across a person’s genome, researchers can calculate a polygenic risk score to estimate someone’s lifetime odds of developing a certain disease. Over the past decade, scientists have developed these risk scores for dozens of diseases, including heart disease, kidney disease, diabetes, and cancer, with the hope that patients could one day use this information to lower any heightened risk of disease. But determining whether such tests work effectively across all populations, and how they can guide clinical decision-making, has been a challenge.</p> <p>Now, a team of researchers at the ӳý of MIT and Harvard, in collaboration with 10 academic medical centers across the US, has implemented 10 such tests for use in clinical research. In a study published today in <a href="https://www.nature.com/articles/s41591-024-02796-z"><em>Nature Medicine</em></a>, the team outlined how they selected, optimized, and validated the tests for 10 common diseases, including heart disease, breast cancer, and type 2 diabetes. They also calibrated the tests for use in people with non-European ancestries.</p> <p>The scientists worked in collaboration with the national <a href="https://emerge-network.org/">Electronic Medical Records and Genomics (eMERGE) network</a>, which is funded by the National Human Genome Research Institute to study how patients’ genetic data can be integrated with their electronic medical records to improve clinical care and health outcomes. The 10 collaborating medical centers are part of the project and enrolling 25,000 participants for it, while researchers at <a href="https://broadclinicallabs.org/">ӳý Clinical Labs</a>, a subsidiary of the ӳý, carry out the polygenic risk score testing for those participants.</p> <p>“There have been a lot of ongoing conversations and debates about polygenic risk scores and their utility and applicability in the clinical setting,” said <a href="/bios/niall-lennon">Niall Lennon</a>, chief scientific officer of ӳý Clinical Labs, an institute scientist at ӳý, and first author of the new paper. “With this work, we’ve taken the first steps toward showing the potential strength and power of these scores across a diverse population. We hope in the future this kind of information can be used in preventive medicine to help people take actions that lower their risk of disease.”</p> <h2>What’s the score?</h2> <p>Most polygenic risk scores have been developed based on genetic data largely from people of European ancestry, raising questions about whether the scores are applicable to people of other ancestries.</p> <p>To optimize polygenic risk scores for a diversity of people, Lennon and his colleagues first combed the literature looking for polygenic risk scores that had been tested in people from at least two different genetic ancestries. They also searched for scores that indicate a disease risk that patients could reduce with medical treatments, screening, and/or lifestyle changes. &nbsp;</p> <p>“It was important that we weren’t giving people results that they couldn’t do anything about,” said Lennon.</p> <p>The team selected 10 conditions to focus on for polygenic risk scores: atrial fibrillation, breast cancer, chronic kidney disease, coronary heart disease, hypercholesterolemia, prostate cancer, asthma, type 1 diabetes, obesity, and type 2 diabetes.&nbsp;</p> <p>For each condition, the researchers identified the exact spots in the genome that they would analyze to calculate the risk score. They verified that all those spots could be accurately genotyped, by comparing the results of their tests with whole genome sequences from each patient’s blood sample.</p> <p>Finally, the researchers wanted to make polygenic risk scores work across different genetic ancestries. They studied how genetic variants differ across populations by analyzing data from the National Institutes of Health’s All of Us research program, which is collecting health information from one million people from diverse backgrounds across the U.S. The team used that information to create a model to calibrate a person’s polygenic risk score according to that individual’s genetic ancestry.</p> <p>“We can’t fix all biases in the risk scores, but we can make sure that if a person is in a high-risk group for a disease, they’ll get identified as high risk regardless of what their genetic ancestry is,” explained Lennon.</p> <p>With that optimization complete, Lennon’s team at ӳý Clinical Labs ended up with 10 tests that they are now using to calculate risk scores for the 25,000 people enrolled in the eMERGE study. With their eMERGE collaborators, they are also planning detailed follow-up studies to analyze how polygenic risk scores might influence patients’ health care.</p> <p>“Ultimately, the network wants to know what it means for a person to receive information that says they’re at high risk for one of these diseases,” Lennon said.<br> &nbsp;</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro paragraph--view-mode--default"> <div class="field field--name-field-paragraph field--type-entity-reference-revisions field--label-hidden field__items"> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Funding</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>This phase of the eMERGE Network was initiated and funded by the National Human Genome Research Institute.</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Paper cited:</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>Lennon, NJ. et al. <a href="https://www.nature.com/articles/s41591-024-02796-z">Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations</a>. <em>Nature Medicine</em>. Online February 19, 2024. DOI: 10.1038/s41591-024-02796-z</p> </div> </div> </div> </div> </div> </div> </div> </div> </div> </div> <div class="content-section container"> <div class="content-section__main"> <div class="block-node-broad-tags block block-layout-builder block-field-blocknodelong-storyfield-broad-tags"> <div class="block-node-broad-tags__row"> <div class="block-node-broad-tags__title">Tags:</div> <div class="field field--name-field-broad-tags field--type-entity-reference field--label-hidden field__items"> <div class="field__item"><a href="/broad-tags/broad-clinical-labs" hreflang="en">ӳý Clinical Labs</a></div> <div class="field__item"><a href="/broad-tags/using-genomics-predict-disease-risk" hreflang="en">Using genomics to predict disease risk</a></div> </div> </div> </div> </div> </div> Thu, 08 Oct 2020 04:00:00 +0000 tulrich@broadinstitute.org 660191 at Genetic information can predict predisposition to rare and common blood diseases /news/genetic-information-can-predict-predisposition-rare-and-common-blood-diseases <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> <span class="field field--name-uid field--type-entity-reference field--label-hidden"> <span>By Corie Lok</span> </span> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" class="datetime">February 19, 2024</time> </span> <div class="hero-section container"> <div class="hero-section__row row"> <div class="hero-section__content hero-section__content_left col-6"> <div class="hero-section__breadcrumbs"> <div class="block block-system block-system-breadcrumb-block"> <nav class="breadcrumb" role="navigation" aria-labelledby="system-breadcrumb"> <h2 id="system-breadcrumb" class="visually-hidden">Breadcrumb</h2> <ol> <li> <a href="/">Home</a> </li> <li> <a href="/news">News</a> </li> </ol> </nav> </div> </div> <div class="hero-section__title"> <div class="block block-layout-builder block-field-blocknodelong-storytitle"> <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> </div> </div> <div class="hero-section__description"> <div class="block block-layout-builder block-field-blocknodelong-storybody"> <div class="clearfix text-formatted field field--name-body field--type-text-with-summary field--label-hidden field__item"><p>As part of a nationwide collaboration, ӳý Clinical Labs researchers have optimized 10 polygenic scores for use in clinical research as part of a study on how to implement genetic risk prediction for patients.</p> </div> </div> </div> <div class="hero-section__author"> <div class="block block-layout-builder block-extra-field-blocknodelong-storyextra-field-author-custom"> By Sarah C.P. Williams </div> </div> <div class="hero-section__date"> <div class="block block-layout-builder block-field-blocknodelong-storycreated"> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" title="Monday, February 19, 2024 - 11:00" class="datetime">February 19, 2024</time> </span> </div> </div> </div> <div class="hero-section__right col-6"> <div class="hero-section__image"> <div class="block block-layout-builder block-field-blocknodelong-storyfield-image"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"> <article class="media media--type-image media--view-mode-multiple-content-types-header"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <picture> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1921px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop/public/longstory/PRS_image.png?itok=2jyY3u4P 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="736" height="520"> <source srcset="/files/styles/multiple_ct_header_laptop/public/longstory/PRS_image.png?itok=pkoJbldP 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="641" height="451"> <source srcset="/files/styles/multiple_ct_header_tablet/public/longstory/PRS_image.png?itok=eKNyOfkD 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="706" height="417"> <source srcset="/files/styles/multiple_ct_header_phone/public/longstory/PRS_image.png?itok=drWXPi5h 1x" media="all and (max-width: 539px)" type="image/png" width="499" height="294"> <img loading="eager" src="/files/styles/multiple_ct_header_phone/public/longstory/PRS_image.png?itok=drWXPi5h" width="499" height="294" alt="Graphic highlighting different spots in a genetic sequence" title="Graphic highlighting different spots in a genetic sequence" typeof="foaf:Image"> </picture> </div> <div class="media-caption"> <div class="media-caption__description"> </div> </div> </article> </div> </div> </div> </div> </div> </div> <div class="content-section container"> <div class="content-section__main"> <div class="block block-better-social-sharing-buttons block-social-sharing-buttons-block"> <div style="display: none"><link rel="preload" href="/modules/contrib/better_social_sharing_buttons/assets/dist/sprites/social-icons--no-color.svg" as="image" type="image/svg+xml" crossorigin="anonymous"></div> <div class="social-sharing-buttons"> <a href="https://www.facebook.com/sharer/sharer.php?u=/taxonomy/term/1841/feed&amp;title=" 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chief scientific officer and chair of the board of BCL" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">Q&amp;A: ӳý’s newly renamed clinical lab marks a turning point for the institute’s Genomics Platform</span> </a> </div> </article> </div> </div> </div> </div> </div> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>By analyzing millions of small genetic differences across a person’s genome, researchers can calculate a polygenic risk score to estimate someone’s lifetime odds of developing a certain disease. Over the past decade, scientists have developed these risk scores for dozens of diseases, including heart disease, kidney disease, diabetes, and cancer, with the hope that patients could one day use this information to lower any heightened risk of disease. But determining whether such tests work effectively across all populations, and how they can guide clinical decision-making, has been a challenge.</p> <p>Now, a team of researchers at the ӳý of MIT and Harvard, in collaboration with 10 academic medical centers across the US, has implemented 10 such tests for use in clinical research. In a study published today in <a href="https://www.nature.com/articles/s41591-024-02796-z"><em>Nature Medicine</em></a>, the team outlined how they selected, optimized, and validated the tests for 10 common diseases, including heart disease, breast cancer, and type 2 diabetes. They also calibrated the tests for use in people with non-European ancestries.</p> <p>The scientists worked in collaboration with the national <a href="https://emerge-network.org/">Electronic Medical Records and Genomics (eMERGE) network</a>, which is funded by the National Human Genome Research Institute to study how patients’ genetic data can be integrated with their electronic medical records to improve clinical care and health outcomes. The 10 collaborating medical centers are part of the project and enrolling 25,000 participants for it, while researchers at <a href="https://broadclinicallabs.org/">ӳý Clinical Labs</a>, a subsidiary of the ӳý, carry out the polygenic risk score testing for those participants.</p> <p>“There have been a lot of ongoing conversations and debates about polygenic risk scores and their utility and applicability in the clinical setting,” said <a href="/bios/niall-lennon">Niall Lennon</a>, chief scientific officer of ӳý Clinical Labs, an institute scientist at ӳý, and first author of the new paper. “With this work, we’ve taken the first steps toward showing the potential strength and power of these scores across a diverse population. We hope in the future this kind of information can be used in preventive medicine to help people take actions that lower their risk of disease.”</p> <h2>What’s the score?</h2> <p>Most polygenic risk scores have been developed based on genetic data largely from people of European ancestry, raising questions about whether the scores are applicable to people of other ancestries.</p> <p>To optimize polygenic risk scores for a diversity of people, Lennon and his colleagues first combed the literature looking for polygenic risk scores that had been tested in people from at least two different genetic ancestries. They also searched for scores that indicate a disease risk that patients could reduce with medical treatments, screening, and/or lifestyle changes. &nbsp;</p> <p>“It was important that we weren’t giving people results that they couldn’t do anything about,” said Lennon.</p> <p>The team selected 10 conditions to focus on for polygenic risk scores: atrial fibrillation, breast cancer, chronic kidney disease, coronary heart disease, hypercholesterolemia, prostate cancer, asthma, type 1 diabetes, obesity, and type 2 diabetes.&nbsp;</p> <p>For each condition, the researchers identified the exact spots in the genome that they would analyze to calculate the risk score. They verified that all those spots could be accurately genotyped, by comparing the results of their tests with whole genome sequences from each patient’s blood sample.</p> <p>Finally, the researchers wanted to make polygenic risk scores work across different genetic ancestries. They studied how genetic variants differ across populations by analyzing data from the National Institutes of Health’s All of Us research program, which is collecting health information from one million people from diverse backgrounds across the U.S. The team used that information to create a model to calibrate a person’s polygenic risk score according to that individual’s genetic ancestry.</p> <p>“We can’t fix all biases in the risk scores, but we can make sure that if a person is in a high-risk group for a disease, they’ll get identified as high risk regardless of what their genetic ancestry is,” explained Lennon.</p> <p>With that optimization complete, Lennon’s team at ӳý Clinical Labs ended up with 10 tests that they are now using to calculate risk scores for the 25,000 people enrolled in the eMERGE study. With their eMERGE collaborators, they are also planning detailed follow-up studies to analyze how polygenic risk scores might influence patients’ health care.</p> <p>“Ultimately, the network wants to know what it means for a person to receive information that says they’re at high risk for one of these diseases,” Lennon said.<br> &nbsp;</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro paragraph--view-mode--default"> <div class="field field--name-field-paragraph field--type-entity-reference-revisions field--label-hidden field__items"> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Funding</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>This phase of the eMERGE Network was initiated and funded by the National Human Genome Research Institute.</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Paper cited:</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>Lennon, NJ. et al. <a href="https://www.nature.com/articles/s41591-024-02796-z">Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations</a>. <em>Nature Medicine</em>. Online February 19, 2024. DOI: 10.1038/s41591-024-02796-z</p> </div> </div> </div> </div> </div> </div> </div> </div> </div> </div> <div class="content-section container"> <div class="content-section__main"> <div class="block-node-broad-tags block block-layout-builder block-field-blocknodelong-storyfield-broad-tags"> <div class="block-node-broad-tags__row"> <div class="block-node-broad-tags__title">Tags:</div> <div class="field field--name-field-broad-tags field--type-entity-reference field--label-hidden field__items"> <div class="field__item"><a href="/broad-tags/broad-clinical-labs" hreflang="en">ӳý Clinical Labs</a></div> <div class="field__item"><a href="/broad-tags/using-genomics-predict-disease-risk" hreflang="en">Using genomics to predict disease risk</a></div> </div> </div> </div> </div> </div> Thu, 03 Sep 2020 15:46:52 +0000 tulrich@broadinstitute.org 647171 at Genetic background influences disease risk from single-gene variants /news/genetic-background-influences-disease-risk-single-gene-variants <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> <span class="field field--name-uid field--type-entity-reference field--label-hidden"> <span>By Corie Lok</span> </span> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" class="datetime">February 19, 2024</time> </span> <div class="hero-section container"> <div class="hero-section__row row"> <div class="hero-section__content hero-section__content_left col-6"> <div class="hero-section__breadcrumbs"> <div class="block block-system block-system-breadcrumb-block"> <nav class="breadcrumb" role="navigation" aria-labelledby="system-breadcrumb"> <h2 id="system-breadcrumb" class="visually-hidden">Breadcrumb</h2> <ol> <li> <a href="/">Home</a> </li> <li> <a href="/news">News</a> </li> </ol> </nav> </div> </div> <div class="hero-section__title"> <div class="block block-layout-builder block-field-blocknodelong-storytitle"> <span class="field field--name-title field--type-string field--label-hidden"><h1>Genetic risk prediction for 10 chronic diseases moves closer to the clinic</h1> </span> </div> </div> <div class="hero-section__description"> <div class="block block-layout-builder block-field-blocknodelong-storybody"> <div class="clearfix text-formatted field field--name-body field--type-text-with-summary field--label-hidden field__item"><p>As part of a nationwide collaboration, ӳý Clinical Labs researchers have optimized 10 polygenic scores for use in clinical research as part of a study on how to implement genetic risk prediction for patients.</p> </div> </div> </div> <div class="hero-section__author"> <div class="block block-layout-builder block-extra-field-blocknodelong-storyextra-field-author-custom"> By Sarah C.P. Williams </div> </div> <div class="hero-section__date"> <div class="block block-layout-builder block-field-blocknodelong-storycreated"> <span class="field field--name-created field--type-created field--label-hidden"><time datetime="2024-02-19T11:00:28-05:00" title="Monday, February 19, 2024 - 11:00" class="datetime">February 19, 2024</time> </span> </div> </div> </div> <div class="hero-section__right col-6"> <div class="hero-section__image"> <div class="block block-layout-builder block-field-blocknodelong-storyfield-image"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"> <article class="media media--type-image media--view-mode-multiple-content-types-header"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <picture> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1921px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop_xl/public/longstory/PRS_image.png?itok=EvvZDCca 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="754" height="503"> <source srcset="/files/styles/multiple_ct_header_desktop/public/longstory/PRS_image.png?itok=2jyY3u4P 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="736" height="520"> <source srcset="/files/styles/multiple_ct_header_laptop/public/longstory/PRS_image.png?itok=pkoJbldP 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="641" height="451"> <source srcset="/files/styles/multiple_ct_header_tablet/public/longstory/PRS_image.png?itok=eKNyOfkD 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="706" height="417"> <source srcset="/files/styles/multiple_ct_header_phone/public/longstory/PRS_image.png?itok=drWXPi5h 1x" media="all and (max-width: 539px)" 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class="field__item"><article about="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=v0H61Dlb 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=v0H61Dlb 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=T5fQXaVN 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=Ed2K9V55 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/polygenic-risk-scores_736x520.png?h=27d9a407&amp;itok=eHDn3BqW" width="220" height="186" alt="Polygenic scores for heart disease" title="Polygenic scores for heart disease" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/more-diverse-datasets-lead-better-genetic-risk-prediction-heart-disease" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">More diverse datasets lead to better genetic risk prediction for heart disease </span> </a> </div> </article> </div> <div class="field__item"><article about="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node"> <div class="field field--name-field-image field--type-entity-reference field--label-hidden field__item"><article class="media media--type-image media--view-mode-multiple-ct-sidebar-link-with-image"> <div class="field field--name-field-media-image field--type-image field--label-hidden field__item"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform"><picture> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1921px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop_xl/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=LZDmSgrJ 1x" media="all and (min-width: 1601px) and (max-width: 1920px)" type="image/png" width="104" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 1340px) and (max-width: 1600px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_desktop/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=WtpBRUxg 1x" media="all and (min-width: 800px) and (max-width: 1339px)" type="image/png" width="87" height="104"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_tablet/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=45Sone65 1x" media="all and (min-width: 540px) and (max-width: 799px)" type="image/png" width="285" height="186"> <source srcset="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0 1x" media="all and (max-width: 539px)" type="image/png" width="220" height="186"> <img loading="eager" src="/files/styles/multiple_ct_sidebar_link_with_image_phone/public/longstory/LennonNiall_QandA.png?h=bda0d0a8&amp;itok=EMmF5FP0" width="220" height="186" alt="Niall Lennon, chief scientific officer and chair of the board of BCL" title="Niall Lennon, chief scientific officer and chair of the board of BCL" typeof="foaf:Image"> </picture></a> </div> </article> </div> <div class="node__content"> <a href="/news/qa-broads-newly-renamed-clinical-lab-marks-turning-point-institutes-genomics-platform" class="node__title"><span class="field field--name-title field--type-string field--label-hidden">Q&amp;A: ӳý’s newly renamed clinical lab marks a turning point for the institute’s Genomics Platform</span> </a> </div> </article> </div> </div> </div> </div> </div> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>By analyzing millions of small genetic differences across a person’s genome, researchers can calculate a polygenic risk score to estimate someone’s lifetime odds of developing a certain disease. Over the past decade, scientists have developed these risk scores for dozens of diseases, including heart disease, kidney disease, diabetes, and cancer, with the hope that patients could one day use this information to lower any heightened risk of disease. But determining whether such tests work effectively across all populations, and how they can guide clinical decision-making, has been a challenge.</p> <p>Now, a team of researchers at the ӳý of MIT and Harvard, in collaboration with 10 academic medical centers across the US, has implemented 10 such tests for use in clinical research. In a study published today in <a href="https://www.nature.com/articles/s41591-024-02796-z"><em>Nature Medicine</em></a>, the team outlined how they selected, optimized, and validated the tests for 10 common diseases, including heart disease, breast cancer, and type 2 diabetes. They also calibrated the tests for use in people with non-European ancestries.</p> <p>The scientists worked in collaboration with the national <a href="https://emerge-network.org/">Electronic Medical Records and Genomics (eMERGE) network</a>, which is funded by the National Human Genome Research Institute to study how patients’ genetic data can be integrated with their electronic medical records to improve clinical care and health outcomes. The 10 collaborating medical centers are part of the project and enrolling 25,000 participants for it, while researchers at <a href="https://broadclinicallabs.org/">ӳý Clinical Labs</a>, a subsidiary of the ӳý, carry out the polygenic risk score testing for those participants.</p> <p>“There have been a lot of ongoing conversations and debates about polygenic risk scores and their utility and applicability in the clinical setting,” said <a href="/bios/niall-lennon">Niall Lennon</a>, chief scientific officer of ӳý Clinical Labs, an institute scientist at ӳý, and first author of the new paper. “With this work, we’ve taken the first steps toward showing the potential strength and power of these scores across a diverse population. We hope in the future this kind of information can be used in preventive medicine to help people take actions that lower their risk of disease.”</p> <h2>What’s the score?</h2> <p>Most polygenic risk scores have been developed based on genetic data largely from people of European ancestry, raising questions about whether the scores are applicable to people of other ancestries.</p> <p>To optimize polygenic risk scores for a diversity of people, Lennon and his colleagues first combed the literature looking for polygenic risk scores that had been tested in people from at least two different genetic ancestries. They also searched for scores that indicate a disease risk that patients could reduce with medical treatments, screening, and/or lifestyle changes. &nbsp;</p> <p>“It was important that we weren’t giving people results that they couldn’t do anything about,” said Lennon.</p> <p>The team selected 10 conditions to focus on for polygenic risk scores: atrial fibrillation, breast cancer, chronic kidney disease, coronary heart disease, hypercholesterolemia, prostate cancer, asthma, type 1 diabetes, obesity, and type 2 diabetes.&nbsp;</p> <p>For each condition, the researchers identified the exact spots in the genome that they would analyze to calculate the risk score. They verified that all those spots could be accurately genotyped, by comparing the results of their tests with whole genome sequences from each patient’s blood sample.</p> <p>Finally, the researchers wanted to make polygenic risk scores work across different genetic ancestries. They studied how genetic variants differ across populations by analyzing data from the National Institutes of Health’s All of Us research program, which is collecting health information from one million people from diverse backgrounds across the U.S. The team used that information to create a model to calibrate a person’s polygenic risk score according to that individual’s genetic ancestry.</p> <p>“We can’t fix all biases in the risk scores, but we can make sure that if a person is in a high-risk group for a disease, they’ll get identified as high risk regardless of what their genetic ancestry is,” explained Lennon.</p> <p>With that optimization complete, Lennon’s team at ӳý Clinical Labs ended up with 10 tests that they are now using to calculate risk scores for the 25,000 people enrolled in the eMERGE study. With their eMERGE collaborators, they are also planning detailed follow-up studies to analyze how polygenic risk scores might influence patients’ health care.</p> <p>“Ultimately, the network wants to know what it means for a person to receive information that says they’re at high risk for one of these diseases,” Lennon said.<br> &nbsp;</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro paragraph--view-mode--default"> <div class="field field--name-field-paragraph field--type-entity-reference-revisions field--label-hidden field__items"> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Funding</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>This phase of the eMERGE Network was initiated and funded by the National Human Genome Research Institute.</p> </div> </div> </div> <div class="field__item"> <div class="paragraph paragraph--type--table-outro-row paragraph--view-mode--default"> <div class="clearfix text-formatted field field--name-field-heading field--type-text field--label-hidden field__item"><p>Paper cited:</p> </div> <div class="clearfix text-formatted field field--name-field-text field--type-text-long field--label-hidden field__item"><p>Lennon, NJ. et al. <a href="https://www.nature.com/articles/s41591-024-02796-z">Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations</a>. <em>Nature Medicine</em>. Online February 19, 2024. DOI: 10.1038/s41591-024-02796-z</p> </div> </div> </div> </div> </div> </div> </div> </div> </div> </div> <div class="content-section container"> <div class="content-section__main"> <div class="block-node-broad-tags block block-layout-builder block-field-blocknodelong-storyfield-broad-tags"> <div class="block-node-broad-tags__row"> <div class="block-node-broad-tags__title">Tags:</div> <div class="field field--name-field-broad-tags field--type-entity-reference field--label-hidden field__items"> <div class="field__item"><a href="/broad-tags/broad-clinical-labs" hreflang="en">ӳý Clinical Labs</a></div> <div class="field__item"><a href="/broad-tags/using-genomics-predict-disease-risk" hreflang="en">Using genomics to predict disease risk</a></div> </div> </div> </div> </div> </div> Thu, 20 Aug 2020 13:45:30 +0000 Corie Lok 641616 at