Počet záznamů: 1  

Common Genetic Variation and Age of Onset of Anorexia Nervosa

  1. 1.
    SYSNO ASEP0576271
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevCommon Genetic Variation and Age of Onset of Anorexia Nervosa
    Tvůrce(i) Watson, H. J. (US)
    Thornton, L. M. (US)
    Yilmaz, Z. (US)
    Baker, J. H. (US)
    Coleman, J. R. I. (GB)
    Adan, R. A. H. (SE)
    Alfredsson, L. (SE)
    Andreassen, O. A. (NO)
    Ask, H. (NO)
    Berrettini, W. H. (US)
    Boehnke, M. (US)
    Boehm, I. (DE)
    Boni, C. (FR)
    Buehren, K. (DE)
    Bulant, J. (CZ)
    Burghardt, R. (DE)
    Chang, X. (US)
    Cichon, S. (DE)
    Cone, R. D. (US)
    Courtet, P. (FR)
    Crow, S. (CH)
    Crowley, J. J. (SE)
    Danner, U. N. (NL)
    de Zwaan, M. (DE)
    Dedoussis, G. (GR)
    DeSocio, J. E. (US)
    Dick, D. M. (US)
    Dikeos, D. (GR)
    Dina, C. (FR)
    Šlachtová, Lenka (UOCHB-X)
    Bulik, C. M. (US)
    Celkový počet autorů178
    Zdroj.dok.Biological Psychiatry. Global Open Science. - : Elsevier - ISSN 2667-1743
    Roč. 2, č. 4 (2022), s. 368-378
    Poč.str.11 s.
    Jazyk dok.eng - angličtina
    Země vyd.US - Spojené státy americké
    Klíč. slovagenome-wide association ; eating disorders ; familial aggregation
    Obor OECDBiochemistry and molecular biology
    Způsob publikováníOpen access
    Institucionální podporaUOCHB-X - RVO:61388963
    UT WOS001050120400008
    EID SCOPUS85129769148
    DOI10.1016/j.bpsgos.2021.09.001
    AnotaceBACKGROUND: 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 earlyonset 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.
    PracovištěÚstav organické chemie a biochemie
    Kontaktasep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Jana Procházková, Tel.: 220 183 418
    Rok sběru2024
    Elektronická adresahttps://doi.org/10.1016/j.bpsgos.2021.09.001
Počet záznamů: 1  

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