Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa.
Authors | |
Keywords | |
Abstract | OBJECTIVE: The authors conducted a genome-wide association study of anorexia nervosa and calculated genetic correlations with a series of psychiatric, educational, and metabolic phenotypes. METHOD: Following uniform quality control and imputation procedures using the 1000 Genomes Project (phase 3) in 12 case-control cohorts comprising 3,495 anorexia nervosa cases and 10,982 controls, the authors performed standard association analysis followed by a meta-analysis across cohorts. Linkage disequilibrium score regression was used to calculate genome-wide common variant heritability (single-nucleotide polymorphism [SNP]-based heritability [h]), partitioned heritability, and genetic correlations (r) between anorexia nervosa and 159 other phenotypes. RESULTS: Results were obtained for 10,641,224 SNPs and insertion-deletion variants with minor allele frequencies >1% and imputation quality scores >0.6. The h of anorexia nervosa was 0.20 (SE=0.02), suggesting that a substantial fraction of the twin-based heritability arises from common genetic variation. The authors identified one genome-wide significant locus on chromosome 12 (rs4622308) in a region harboring a previously reported type 1 diabetes and autoimmune disorder locus. Significant positive genetic correlations were observed between anorexia nervosa and schizophrenia, neuroticism, educational attainment, and high-density lipoprotein cholesterol, and significant negative genetic correlations were observed between anorexia nervosa and body mass index, insulin, glucose, and lipid phenotypes. CONCLUSIONS: Anorexia nervosa is a complex heritable phenotype for which this study has uncovered the first genome-wide significant locus. Anorexia nervosa also has large and significant genetic correlations with both psychiatric phenotypes and metabolic traits. The study results encourage a reconceptualization of this frequently lethal disorder as one with both psychiatric and metabolic etiology. |
Year of Publication | 2017
|
Journal | Am J Psychiatry
|
Volume | 174
|
Issue | 9
|
Pages | 850-858
|
Date Published | 2017 09 01
|
ISSN | 1535-7228
|
DOI | 10.1176/appi.ajp.2017.16121402
|
PubMed ID | 28494655
|
PubMed Central ID | PMC5581217
|
Links | |
Grant list | K01 MH109782 / MH / NIMH NIH HHS / United States
K01 MH106675 / MH / NIMH NIH HHS / United States
WT088827/Z/09 / Wellcome Trust / United Kingdom
R01 DK075787 / DK / NIDDK NIH HHS / United States
CIHR / Canada
K01 MH100435 / MH / NIMH NIH HHS / United States
U01 MH109514 / MH / NIMH NIH HHS / United States
K02 AA018755 / AA / NIAAA NIH HHS / United States
T32 MH076694 / MH / NIMH NIH HHS / United States
G0901245 / Medical Research Council / United Kingdom
K01 MH093750 / MH / NIMH NIH HHS / United States
Wellcome Trust / United Kingdom
U01 MH109539 / MH / NIMH NIH HHS / United States
R01 AA015416 / AA / NIAAA NIH HHS / United States
U01 MH094432 / MH / NIMH NIH HHS / United States
R01 MH092793 / MH / NIMH NIH HHS / United States
U01 MH109528 / MH / NIMH NIH HHS / United States
U01 HG006830 / HG / NHGRI NIH HHS / United States
|