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Genetics of attention deficit hyperactivity disorder

Molecular Psychiatry · 2018 · Vol. 24(4) · pp. 562–575
Stephen V. FaraoneHenrik Larsson

Abstract

Decades of research show that genes play an vital role in the etiology of attention deficit hyperactivity disorder (ADHD) and its comorbidity with other disorders. Family, twin, and adoption studies show that ADHD runs in families. ADHD's high heritability of 74% motivated the search for ADHD susceptibility genes. Genetic linkage studies show that the effects of DNA risk variants on ADHD must, individually, be very small. Genome-wide association studies (GWAS) have implicated several genetic loci at the genome-wide level of statistical significance. These studies also show that about a third of ADHD's heritability is due to a polygenic component comprising many common variants each having small effects. From studies of copy number variants we have also learned that the rare insertions or deletions account for part of ADHD's heritability. These findings have implicated new biological pathways that may eventually have implications for treatment development.

Attention Deficit Hyperactivity DisorderGenetics and Neurodevelopmental DisordersAutism Spectrum Disorder ResearchHeritabilityGenome-wide association studyAttention deficit hyperactivity disorderTwin studyGenetic associationMissing heritability problemGeneticsComorbidityGenetic linkageCandidate gene

MeSH terms

Attention Deficit Disorder with HyperactivityHumansGenetic LinkageGenetic Predisposition to DiseaseMultifactorial InheritanceGenome-Wide Association StudyDNA Copy Number Variations

Funding

  • Eli Lilly and Company
  • European Commission
  • Vetenskapsrådet
  • Universitetet i Bergen
  • H. Lundbeck A/S
  • National Institute of Mental Health
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