COMT Val158Met Polymorphism and Social Impairment Interactively Affect Attention-Deficit Hyperactivity Symptoms in Healthy Adolescents
Publikation: Beitrag in Fachzeitschrift › Forschungsartikel › Beigetragen › Begutachtung
Beitragende
- Universität Heidelberg
- Universität Leipzig
- Trinity College Dublin
- Universität Hamburg
- King's College London (KCL)
- Universität Mannheim
- Commissariat à l’énergie atomique et aux énergies alternatives (CEA)
- University of Vermont
- University of Nottingham
- Charité – Universitätsmedizin Berlin
- Physikalisch-Technische Bundesanstalt
- INSERM - Institut national de la santé et de la recherche médicale
- Service Hospitalier Frederic Joliot
- University of Toronto
- Georg-August-Universität Göttingen
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
Originalsprache | Englisch |
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Aufsatznummer | 284 |
Fachzeitschrift | Frontiers in genetics |
Jahrgang | 9 |
Publikationsstatus | Veröffentlicht - 31 Juli 2018 |
Peer-Review-Status | Ja |
Externe IDs
ORCID | /0000-0001-5398-5569/work/161890753 |
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ORCID | /0000-0002-8493-6396/work/161891665 |
Schlagworte
ASJC Scopus Sachgebiete
Schlagwörter
- ADHD, adolescence, COMT, moderation, social impairment