Meta-analysis of the DRD5 VNTR in persistent ADHD

Marieke Klein, Stefanie Berger, Martine Hoogman, Janneke Dammers, Remco Makkinje, Angelien J.G.A.M. Heister, Tessel E. Galesloot, Lambertus A.L.M. Kiemeney, Heike Weber, Sarah Kittel-Schneider, Klaus Peter Lesch, Andreas Reif, Marta Ribasés, Josep Antoni Ramos-Quiroga, Bru Cormand, Tetyana Zayats, Tor Arne Hegvik, Kaya K. Jacobsen, Stefan Johansson, Jan HaavikNina R. Mota, Claiton H.D. Bau, Eugenio H. Grevet, Alysa Doyle, Stephen V. Faraone, Alejandro Arias-Vásquez, Barbara Franke

Research output: Contribution to journalArticleResearchpeer-review

2 Citations (Scopus)

Abstract

© 2016 Elsevier B.V. and ECNP 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.
Original languageEnglish
Pages (from-to)1527-1532
JournalEuropean Neuropsychopharmacology
Volume26
Issue number9
DOIs
Publication statusPublished - 1 Sep 2016

Keywords

  • Attention-Deficit/Hyperactivity Disorder
  • Candidate gene
  • DRD5
  • Meta-analysis

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