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COMT Val158Met Polymorphism and Social Impairment Interactively Affect Attention-Deficit Hyperactivity Symptoms in Healthy Adolescents
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 rela...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6079264/ https://www.ncbi.nlm.nih.gov/pubmed/30108607 http://dx.doi.org/10.3389/fgene.2018.00284 |
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author | Millenet, Sabina K. Nees, Frauke Heintz, Stefan Bach, Christiane Frank, Josef Vollstädt-Klein, Sabine Bokde, Arun Bromberg, Uli Büchel, Christian Quinlan, Erin B. Desrivières, Sylvane Fröhner, Juliane Flor, Herta Frouin, Vincent Garavan, Hugh Gowland, Penny Heinz, Andreas Ittermann, Bernd Lemaire, Herve Martinot, Jean-Luc Martinot, Marie-Laure P. Papadoulos, Dimitri O. Paus, Tomáš Poustka, Luise Rietschel, Marcella Smolka, Michael N. Walter, Henrik Whelan, Rob Schumann, Gunter Banaschewski, Tobias Hohmann, Sarah |
author_facet | Millenet, Sabina K. Nees, Frauke Heintz, Stefan Bach, Christiane Frank, Josef Vollstädt-Klein, Sabine Bokde, Arun Bromberg, Uli Büchel, Christian Quinlan, Erin B. Desrivières, Sylvane Fröhner, Juliane Flor, Herta Frouin, Vincent Garavan, Hugh Gowland, Penny Heinz, Andreas Ittermann, Bernd Lemaire, Herve Martinot, Jean-Luc Martinot, Marie-Laure P. Papadoulos, Dimitri O. Paus, Tomáš Poustka, Luise Rietschel, Marcella Smolka, Michael N. Walter, Henrik Whelan, Rob Schumann, Gunter Banaschewski, Tobias Hohmann, Sarah |
author_sort | Millenet, Sabina K. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6079264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60792642018-08-14 COMT Val158Met Polymorphism and Social Impairment Interactively Affect Attention-Deficit Hyperactivity Symptoms in Healthy Adolescents Millenet, Sabina K. Nees, Frauke Heintz, Stefan Bach, Christiane Frank, Josef Vollstädt-Klein, Sabine Bokde, Arun Bromberg, Uli Büchel, Christian Quinlan, Erin B. Desrivières, Sylvane Fröhner, Juliane Flor, Herta Frouin, Vincent Garavan, Hugh Gowland, Penny Heinz, Andreas Ittermann, Bernd Lemaire, Herve Martinot, Jean-Luc Martinot, Marie-Laure P. Papadoulos, Dimitri O. Paus, Tomáš Poustka, Luise Rietschel, Marcella Smolka, Michael N. Walter, Henrik Whelan, Rob Schumann, Gunter Banaschewski, Tobias Hohmann, Sarah Front Genet Genetics 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. Frontiers Media S.A. 2018-07-31 /pmc/articles/PMC6079264/ /pubmed/30108607 http://dx.doi.org/10.3389/fgene.2018.00284 Text en Copyright © 2018 Millenet, Nees, Heintz, Bach, Frank, Vollstädt-Klein, Bokde, Bromberg, Büchel, Quinlan, Desrivières, Fröhner, Flor, Frouin, Garavan, Gowland, Heinz, Ittermann, Lemaire, Martinot, Martinot, Papadoulos, Paus, Poustka, Rietschel, Smolka, Walter, Whelan, Schumann, Banaschewski and Hohmann. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Millenet, Sabina K. Nees, Frauke Heintz, Stefan Bach, Christiane Frank, Josef Vollstädt-Klein, Sabine Bokde, Arun Bromberg, Uli Büchel, Christian Quinlan, Erin B. Desrivières, Sylvane Fröhner, Juliane Flor, Herta Frouin, Vincent Garavan, Hugh Gowland, Penny Heinz, Andreas Ittermann, Bernd Lemaire, Herve Martinot, Jean-Luc Martinot, Marie-Laure P. Papadoulos, Dimitri O. Paus, Tomáš Poustka, Luise Rietschel, Marcella Smolka, Michael N. Walter, Henrik Whelan, Rob Schumann, Gunter Banaschewski, Tobias Hohmann, Sarah COMT Val158Met Polymorphism and Social Impairment Interactively Affect Attention-Deficit Hyperactivity Symptoms in Healthy Adolescents |
title | COMT Val158Met Polymorphism and Social Impairment Interactively Affect Attention-Deficit Hyperactivity Symptoms in Healthy Adolescents |
title_full | COMT Val158Met Polymorphism and Social Impairment Interactively Affect Attention-Deficit Hyperactivity Symptoms in Healthy Adolescents |
title_fullStr | COMT Val158Met Polymorphism and Social Impairment Interactively Affect Attention-Deficit Hyperactivity Symptoms in Healthy Adolescents |
title_full_unstemmed | COMT Val158Met Polymorphism and Social Impairment Interactively Affect Attention-Deficit Hyperactivity Symptoms in Healthy Adolescents |
title_short | COMT Val158Met Polymorphism and Social Impairment Interactively Affect Attention-Deficit Hyperactivity Symptoms in Healthy Adolescents |
title_sort | comt val158met polymorphism and social impairment interactively affect attention-deficit hyperactivity symptoms in healthy adolescents |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6079264/ https://www.ncbi.nlm.nih.gov/pubmed/30108607 http://dx.doi.org/10.3389/fgene.2018.00284 |
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