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

  • 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.

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Metadaten
Author:Viola Stella Palladino, Rhiannon McNeillORCiD, Andreas ReifORCiDGND, Sarah Kittel-SchneiderORCiDGND
URN:urn:nbn:de:hebis:30:3-518810
DOI:https://doi.org/10.1097/YPG.0000000000000220
Parent Title (English):Psychiatric Genetics
Document Type:Article
Language:English
Year of Completion:2019
Year of first Publication:2019
Publishing Institution:Universitätsbibliothek Johann Christian Senckenberg
Release Date:2019/12/03
Tag:attention-deficit/hyperactivity disorder; common variant; epigenetics; gene×environment interactions; pharmacogenetics; rare variant; risk genes
Volume:29
First Page:63
Last Page:77
Note:
Gefördert von "European Union's Horizon 2020 research and innovation program, Marie-Curie Training Network; Project name: MiND, Grant agreement no. 643051"
HeBIS-PPN:459855468
Institutes:Medizin / Medizin
Dewey Decimal Classification:6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Sammlungen:Universitätspublikationen
Licence (German):License LogoDeutsches Urheberrecht