Meta-analysis of the DRD5 VNTR in persistent ADHD
Publication year
2016Author(s)
Number of pages
6 p.
Source
European Neuropsychopharmacology, 26, 9, (2016), pp. 1527-1532ISSN
Publication type
Article / Letter to editor
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Organization
Human Genetics
PI Group MR Techniques in Brain Function
Psychiatry
Health Evidence
Urology
Cognitive Neuroscience
Journal title
European Neuropsychopharmacology
Volume
vol. 26
Issue
iss. 9
Languages used
English (eng)
Page start
p. 1527
Page end
p. 1532
Subject
Radboudumc 15: Urological cancers RIHS: Radboud Institute for Health Sciences; Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical NeuroscienceAbstract
Attention-Deficit/Hyperactivity Disorder (ADHD) is a common neuropsychiatric disorder with a complex genetic background. DRD5, the gene encoding the dopamine receptor D5, was recently confirmed as a candidate gene for ADHD in children through meta-analysis. In this study, we aimed at studying the association of the ADHD-associated variable number tandem repeat (VNTR) polymorphism upstream of DRD5 with adult ADHD. We compiled data from six sites of the International Multicentre persistent ADHD CollaboraTion (IMpACT) and reached N=6979 (3344 cases and 3635 healthy participants), the largest sample investigated so far. We tested the association of the common DRD5 alleles with categorically defined ADHD and with inattentive and hyperactive/impulsive symptom counts. Our findings provide evidence that none of the common DRD5 alleles are associated with ADHD risk or ADHD symptom counts in adults.
This item appears in the following Collection(s)
- Academic publications [243908]
- Donders Centre for Cognitive Neuroimaging [3982]
- Electronic publications [130670]
- Faculty of Medical Sciences [92803]
- Open Access publications [104958]
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