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

Authors :
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
Source :
Frontiers in Genetics, Vol 9 (2018)
Publication Year :
2018
Publisher :
Frontiers Media S.A., 2018.

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.

Details

Language :
English
ISSN :
16648021
Volume :
9
Database :
Directory of Open Access Journals
Journal :
Frontiers in Genetics
Publication Type :
Academic Journal
Accession number :
edsdoj.23e5444342ca4331a1f5736b3c61dc90
Document Type :
article
Full Text :
https://doi.org/10.3389/fgene.2018.00284