COMT Val158Met Polymorphism and Social Impairment Interactively Affect Attention-Deficit Hyperactivity Symptoms in Healthy Adolescents

  • Sabina K Millenet
  • Frauke Nees
  • Stefan Heintz
  • Christiane Bach
  • Josef Frank
  • Sabine Vollstädt-Klein
  • Arun Bokde
  • Uli Bromberg
  • Christian Büchel
  • Erin B Quinlan
  • Sylvane Desrivières
  • Juliane Fröhner
  • Herta Flor
  • Vincent Frouin
  • Hugh Garavan
  • Penny Gowland
  • Andreas Heinz
  • Bernd Ittermann
  • Herve Lemaire
  • Jean-Luc Martinot
  • Marie-Laure P Martinot
  • Dimitri O Papadoulos
  • Tomáš Paus
  • Luise Poustka
  • Marcella Rietschel
  • Michael N Smolka
  • Henrik Walter
  • Rob Whelan
  • Gunter Schumann
  • Tobias Banaschewski
  • Sarah Hohmann

Abstract

The dopaminergic system has been shown to have substantial effects on the etiology of attention-deficit hyperactivity disorder (ADHD). However, while some studies found a significant direct effect, others did not. In this context, social behavior might play an important role as a factor that is related both to the dopaminergic system and ADHD. In a large epidemiological sample of adolescents (N = 462; 16-17 years), we assessed the level of ADHD symptoms using the Strengths and Difficulties Questionnaire, social behavior using the Social Responsiveness Scale, and the allelic distribution of the dopaminergic catechol-O-methyltransferase (COMT) Val158Met polymorphism. We found a significant association between COMT and social impairment, insofar as Met-allele carriers showed increased levels of social impairment. Moreover, social impairment significantly determined an association between COMT and ADHD (explained variance: 19.09%). This effect did not significantly differ between males and females. COMT and social impairment might interactively affect ADHD symptomatology, and could thus represent significant gene-phenotypic risk factors for ADHD symptomatology. This might have interesting implications for prevention and intervention strategies with a focus on social behavior in genetically at-risk individuals.

Bibliografische Daten

OriginalspracheEnglisch
ISSN1664-8021
DOIs
StatusVeröffentlicht - 2018
PubMed 30108607