TY - JOUR
T1 - Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains
AU - Demontis, Ditte
AU - Walters, G Bragi
AU - Athanasiadis, Georgios
AU - Walters, Raymond
AU - Therrien, Karen
AU - Nielsen, Trine Tollerup
AU - Farajzadeh, Leila
AU - Voloudakis, Georgios
AU - Bendl, Jaroslav
AU - Zeng, Biau
AU - Zhang, Wen
AU - Grove, Jakob
AU - Als, Thomas D
AU - Duan, Jinjie
AU - Satterstrom, F Kyle
AU - Bybjerg-Grauholm, Jonas
AU - Bækved-Hansen, Marie
AU - Gudmundsson, Olafur O
AU - Magnusson, Sigurdur H
AU - Baldursson, Gisli
AU - Davidsdottir, Katrin
AU - Haraldsdottir, Gyda S
AU - Agerbo, Esben
AU - Hoffman, Gabriel E
AU - Dalsgaard, Søren
AU - Martin, Joanna
AU - Ribasés, Marta
AU - Boomsma, Dorret I
AU - Soler Artigas, Maria
AU - Roth Mota, Nina
AU - Howrigan, Daniel
AU - Medland, Sarah E
AU - Zayats, Tetyana
AU - Rajagopal, Veera M
AU - Nordentoft, Merete
AU - Mors, Ole
AU - Hougaard, David M
AU - Mortensen, Preben Bo
AU - Daly, Mark J
AU - Faraone, Stephen V
AU - Stefansson, Hreinn
AU - Roussos, Panos
AU - Franke, Barbara
AU - Werge, Thomas
AU - Neale, Benjamin M
AU - Stefansson, Kari
AU - Børglum, Anders D
AU - ADHD Working Group of the Psychiatric Genomics Consortium
N1 - © 2023. The Author(s), under exclusive licence to Springer Nature America, Inc.
PY - 2023/2
Y1 - 2023/2
N2 - Attention-deficit hyperactivity disorder (ADHD) is a prevalent neurodevelopmental disorder with a major genetic component. Here, we present a genome-wide association study meta-analysis of ADHD comprising 38,691 individuals with ADHD and 186,843 controls. We identified 27 genome-wide significant loci, highlighting 76 potential risk genes enriched among genes expressed particularly in early brain development. Overall, ADHD genetic risk was associated with several brain-specific neuronal subtypes and midbrain dopaminergic neurons. In exome-sequencing data from 17,896 individuals, we identified an increased load of rare protein-truncating variants in ADHD for a set of risk genes enriched with probable causal common variants, potentially implicating SORCS3 in ADHD by both common and rare variants. Bivariate Gaussian mixture modeling estimated that 84-98% of ADHD-influencing variants are shared with other psychiatric disorders. In addition, common-variant ADHD risk was associated with impaired complex cognition such as verbal reasoning and a range of executive functions, including attention.
AB - Attention-deficit hyperactivity disorder (ADHD) is a prevalent neurodevelopmental disorder with a major genetic component. Here, we present a genome-wide association study meta-analysis of ADHD comprising 38,691 individuals with ADHD and 186,843 controls. We identified 27 genome-wide significant loci, highlighting 76 potential risk genes enriched among genes expressed particularly in early brain development. Overall, ADHD genetic risk was associated with several brain-specific neuronal subtypes and midbrain dopaminergic neurons. In exome-sequencing data from 17,896 individuals, we identified an increased load of rare protein-truncating variants in ADHD for a set of risk genes enriched with probable causal common variants, potentially implicating SORCS3 in ADHD by both common and rare variants. Bivariate Gaussian mixture modeling estimated that 84-98% of ADHD-influencing variants are shared with other psychiatric disorders. In addition, common-variant ADHD risk was associated with impaired complex cognition such as verbal reasoning and a range of executive functions, including attention.
KW - Attention Deficit Disorder with Hyperactivity/genetics
KW - Brain
KW - Cognition
KW - Genetic Predisposition to Disease
KW - Genome-Wide Association Study
KW - Humans
UR - http://www.scopus.com/inward/record.url?scp=85146989048&partnerID=8YFLogxK
U2 - 10.1038/s41588-022-01285-8
DO - 10.1038/s41588-022-01285-8
M3 - Journal article
C2 - 36702997
SN - 1061-4036
VL - 55
SP - 198
EP - 208
JO - Nature Genetics
JF - Nature Genetics
IS - 2
ER -