A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4480473
Author(s) Martin, Joanna; Walters, Raymond K.; Demontis, Ditte; Mattheisen, Manuel; Lee, S. Hong; Robinson, Elise; Brikell, Isabell; Ghirardi, Laura; Larsson, Henrik; Lichtenstein, Paul; Eriksson, Nicholas; Mountain View, California.; Psychiatric Genomics Consortium: Adhd Subgroup,; iPsych–Broad Adhd Workgroup,; Werge, Thomas; Mortensen, Preben Bo; Pedersen, Marianne Giørtz; Mors, Ole; Nordentoft, Merete; Hougaard, David M.; Bybjerg-Grauholm, Jonas; Wray, Naomi R.; Franke, Barbara; Faraone, Stephen V.; O'Donovan, Michael C.; Thapar, Anita; Børglum, Anders D.; Neale, Benjamin M.
Author(s) at UniBasel Steinhausen, Hans-Christoph
Year 2018
Title A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder
Journal Biological Psychiatry
Volume 83
Number 12
Pages / Article-Number 1044-1053
Abstract Attention-deficit/hyperactivity disorder (ADHD) shows substantial heritability and is two to seven times more common in male individuals than in female individuals. We examined two putative genetic mechanisms underlying this sex bias: sex-specific heterogeneity and higher burden of risk in female cases.; We analyzed genome-wide autosomal common variants from the Psychiatric Genomics Consortium and iPSYCH Project (n = 20,183 cases, n = 35,191 controls) and Swedish population register data (n = 77,905 cases, n = 1,874,637 population controls).; Genetic correlation analyses using two methods suggested near complete sharing of common variant effects across sexes, with r; g; estimates close to 1. Analyses of population data, however, indicated that female individuals with ADHD may be at especially high risk for certain comorbid developmental conditions (i.e., autism spectrum disorder and congenital malformations), potentially indicating some clinical and etiological heterogeneity. Polygenic risk score analysis did not support a higher burden of ADHD common risk variants in female cases (odds ratio [confidence interval] = 1.02 [0.98-1.06], p = .28). In contrast, epidemiological sibling analyses revealed that the siblings of female individuals with ADHD are at higher familial risk for ADHD than the siblings of affected male individuals (odds ratio [confidence interval] = 1.14 [1.11-1.18], p = 1.5E-15).; Overall, this study supports a greater familial burden of risk in female individuals with ADHD and some clinical and etiological heterogeneity, based on epidemiological analyses. However, molecular genetic analyses suggest that autosomal common variants largely do not explain the sex bias in ADHD prevalence.
Publisher Elsevier
ISSN/ISBN 0006-3223 ; 1873-2402
edoc-URL https://edoc.unibas.ch/64625/
Full Text on edoc No
Digital Object Identifier DOI 10.1016/j.biopsych.2017.11.026
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/29325848
 
   

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