TY - JOUR
T1 - Common Genetic Variation and Age of Onset of Anorexia Nervosa
AU - Watson, Hunna J.
AU - Thornton, Laura M.
AU - Yilmaz, Zeynep
AU - Baker, Jessica H.
AU - Coleman, Jonathan R.I.
AU - Adan, Roger A.H.
AU - Alfredsson, Lars
AU - Andreassen, Ole A.
AU - Ask, Helga
AU - Berrettini, Wade H.
AU - Boehnke, Michael
AU - Boehm, Ilka
AU - Boni, Claudette
AU - Buehren, Katharina
AU - Bulant, Josef
AU - Burghardt, Roland
AU - Chang, Xiao
AU - Cichon, Sven
AU - Cone, Roger D.
AU - Courtet, Philippe
AU - Crow, Scott
AU - Crowley, James J.
AU - Danner, Unna N.
AU - de Zwaan, Martina
AU - Dedoussis, George
AU - DeSocio, Janiece E.
AU - Dick, Danielle M.
AU - Dikeos, Dimitris
AU - Dina, Christian
AU - Djurovic, Srdjan
AU - Dmitrzak-Weglarz, Monika
AU - Docampo-Martinez, Elisa
AU - Duriez, Philibert
AU - Egberts, Karin
AU - Ehrlich, Stefan
AU - Eriksson, Johan G.
AU - Escaramís, Geòrgia
AU - Esko, Tõnu
AU - Estivill, Xavier
AU - Farmer, Anne
AU - Fernández-Aranda, Fernando
AU - Fichter, Manfred M.
AU - Föcker, Manuel
AU - Foretova, Lenka
AU - Forstner, Andreas J.
AU - Frei, Oleksandr
AU - Kas, Martien J.H.
AU - Lin, Bochao
AU - Luykx, Jurjen
AU - Ophoff, Roel A.
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2022/10
Y1 - 2022/10
N2 - Background: Genetics and biology may influence the age of onset of anorexia nervosa (AN). The aims of this study were to determine whether common genetic variation contributes to age of onset of AN and to investigate the genetic associations between age of onset of AN and age at menarche. Methods: A secondary analysis of the Psychiatric Genomics Consortium genome-wide association study (GWAS) of AN was performed, which included 9335 cases and 31,981 screened controls, all from European ancestries. We conducted GWASs of age of onset, early-onset AN (<13 years), and typical-onset AN, and genetic correlation, genetic risk score, and Mendelian randomization analyses. Results: Two loci were genome-wide significant in the typical-onset AN GWAS. Heritability estimates (single nucleotide polymorphism–h2) were 0.01–0.04 for age of onset, 0.16–0.25 for early-onset AN, and 0.17–0.25 for typical-onset AN. Early- and typical-onset AN showed distinct genetic correlation patterns with putative risk factors for AN. Specifically, early-onset AN was significantly genetically correlated with younger age at menarche, and typical-onset AN was significantly negatively genetically correlated with anthropometric traits. Genetic risk scores for age of onset and early-onset AN estimated from independent GWASs significantly predicted age of onset. Mendelian randomization analysis suggested a causal link between younger age at menarche and early-onset AN. Conclusions: Our results provide evidence consistent with a common variant genetic basis for age of onset and implicate biological pathways regulating menarche and reproduction.
AB - Background: Genetics and biology may influence the age of onset of anorexia nervosa (AN). The aims of this study were to determine whether common genetic variation contributes to age of onset of AN and to investigate the genetic associations between age of onset of AN and age at menarche. Methods: A secondary analysis of the Psychiatric Genomics Consortium genome-wide association study (GWAS) of AN was performed, which included 9335 cases and 31,981 screened controls, all from European ancestries. We conducted GWASs of age of onset, early-onset AN (<13 years), and typical-onset AN, and genetic correlation, genetic risk score, and Mendelian randomization analyses. Results: Two loci were genome-wide significant in the typical-onset AN GWAS. Heritability estimates (single nucleotide polymorphism–h2) were 0.01–0.04 for age of onset, 0.16–0.25 for early-onset AN, and 0.17–0.25 for typical-onset AN. Early- and typical-onset AN showed distinct genetic correlation patterns with putative risk factors for AN. Specifically, early-onset AN was significantly genetically correlated with younger age at menarche, and typical-onset AN was significantly negatively genetically correlated with anthropometric traits. Genetic risk scores for age of onset and early-onset AN estimated from independent GWASs significantly predicted age of onset. Mendelian randomization analysis suggested a causal link between younger age at menarche and early-onset AN. Conclusions: Our results provide evidence consistent with a common variant genetic basis for age of onset and implicate biological pathways regulating menarche and reproduction.
KW - Age of onset
KW - Anorexia nervosa
KW - Early-onset
KW - Genetic risk score
KW - Genetics
KW - GWAS
KW - Menarche
KW - Mendelian randomization
KW - Puberty
UR - http://www.scopus.com/inward/record.url?scp=85129769148&partnerID=8YFLogxK
U2 - 10.1016/j.bpsgos.2021.09.001
DO - 10.1016/j.bpsgos.2021.09.001
M3 - Article
AN - SCOPUS:85129769148
SN - 2667-1743
VL - 2
SP - 368
EP - 378
JO - Biological psychiatry global open science
JF - Biological psychiatry global open science
IS - 4
ER -