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Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder.

Ditte DemontisRaymond K WaltersVeera Manikandan RajagopalIrwin D WaldmanJakob GroveThomas Damm AlsSøren DalsgaardMarta RibasesJonas Byberg-GrauholmMaria Bækvad-HansenThomas M WergeMerete NordentoftOle MorsPreben Bo Mortensennull nullBru CormandDavid Michael HougaardBenjamin M NealeBarbara FrankeStephen V FaraoneAnders Dupont Børglum
Published in: Nature communications (2021)
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 = 3.15×10-10, OR = 1.17). We find a higher SNP heritability for ADHD + DBDs (h2SNP = 0.34) when compared to ADHD without DBDs (h2SNP = 0.20), high genetic correlations between ADHD + DBDs and aggressive (rg = 0.81) and anti-social behaviors (rg = 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.
Keyphrases
  • attention deficit hyperactivity disorder
  • autism spectrum disorder
  • genome wide
  • working memory
  • copy number
  • dna methylation
  • mental health
  • healthcare
  • genome wide association study