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Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder.
- Source :
-
Nature communications [Nat Commun] 2021 Jan 25; Vol. 12 (1), pp. 576. Date of Electronic Publication: 2021 Jan 25. - Publication Year :
- 2021
-
Abstract
- Attention-Deficit/Hyperactivity Disorder (ADHD) is a childhood psychiatric disorder often comorbid with disruptive behavior disorders (DBDs). Here, we report a GWAS meta-analysis of ADHD comorbid with DBDs (ADHD + DBDs) including 3802 cases and 31,305 controls. We identify three genome-wide significant loci on chromosomes 1, 7, and 11. A meta-analysis including a Chinese cohort supports that the locus on chromosome 11 is a strong risk locus for ADHD + DBDs across European and Chinese ancestries (rs7118422, P = 3.15×10 <superscript>-10</superscript> , OR = 1.17). We find a higher SNP heritability for ADHD + DBDs (h <superscript>2</superscript> <subscript>SNP</subscript> = 0.34) when compared to ADHD without DBDs (h <superscript>2</superscript> <subscript>SNP</subscript> = 0.20), high genetic correlations between ADHD + DBDs and aggressive (r <subscript>g</subscript> = 0.81) and anti-social behaviors (r <subscript>g</subscript> = 0.82), and an increased burden (polygenic score) of variants associated with ADHD and aggression in ADHD + DBDs compared to ADHD without DBDs. Our results suggest an increased load of common risk variants in ADHD + DBDs compared to ADHD without DBDs, which in part can be explained by variants associated with aggressive behavior.
- Subjects :
- Attention Deficit Disorder with Hyperactivity epidemiology
Attention Deficit and Disruptive Behavior Disorders epidemiology
Child
China epidemiology
Cohort Studies
Comorbidity
Europe epidemiology
Female
Humans
Male
Risk Factors
Attention Deficit Disorder with Hyperactivity genetics
Attention Deficit and Disruptive Behavior Disorders genetics
Genetic Predisposition to Disease genetics
Genome-Wide Association Study methods
Multifactorial Inheritance genetics
Polymorphism, Single Nucleotide
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 12
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 33495439
- Full Text :
- https://doi.org/10.1038/s41467-020-20443-2