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Genetic risk factors and gene-environment interactions in adult and childhood attention-deficit/hyperactivity disorder

Journal

PSYCHIATRIC GENETICS
Volume 29, Issue 3, Pages 63-78

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/YPG.0000000000000220

Keywords

attention-deficit/hyperactivity disorder; common variant; epigenetics; genexenvironment interactions; pharmacogenetics; rare variant; risk genes

Funding

  1. European Union's Horizon 2020 research and innovation program [643051]
  2. EU [667302]
  3. DAAD [91690211]

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Attention-deficit/hyperactivity disorder (ADHD) is a common and highly heritable neurodevelopmental disorder. In recent years, genetic studies have revealed several risk gene variants associated with ADHD; however, these variants could only be partly replicated and are responsible for only a fraction of the whole heritability of ADHD estimated from family and twin studies. One factor that could potentially explain the 'missing heritability' of ADHD is that childhood and adult or persistent ADHD could be genetically distinct subtypes, which therefore need to be analyzed separately. Another approach to identify this missing heritability could be combining the investigation of both common and rare gene risk variants as well as polygenic risk scores. Finally, environmental factors are also thought to play an important role in the etiology of ADHD, acting either independently of the genetic background or more likely in gene-environment interactions. Environmental factors might additionally convey their influence by epigenetic mechanisms, which are relatively underexplored in ADHD. The aforementioned mechanisms might also influence the response of patients with ADHD to stimulant and other ADHD medication. We conducted a selective review with a focus on risk genes of childhood and adult ADHD, gene-environment interactions, and pharmacogenetics studies on medication response in childhood and adult ADHD. Copyright (C) 2019 Wolters Kluwer Health, Inc. All rights reserved.

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