Cargando…

The interaction between 5-HTTLPR and stress exposure influences connectivity of the executive control and default mode brain networks

We recently reported that the serotonin transporter polymorphism 5-HTTLPR moderates the relation between stress exposure and attention-deficit/hyperactivity disorder (ADHD) severity. This gene-environment interaction (GxE) has been previously tied to the processing of emotional stimuli, which is inc...

Descripción completa

Detalles Bibliográficos
Autores principales: van der Meer, Dennis, Hartman, Catharina A., Pruim, Raimon H. R., Mennes, Maarten, Heslenfeld, Dirk, Oosterlaan, Jaap, Faraone, Stephen V., Franke, Barbara, Buitelaar, Jan K., Hoekstra, Pieter J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653701/
https://www.ncbi.nlm.nih.gov/pubmed/27738993
http://dx.doi.org/10.1007/s11682-016-9633-3
_version_ 1783273257073377280
author van der Meer, Dennis
Hartman, Catharina A.
Pruim, Raimon H. R.
Mennes, Maarten
Heslenfeld, Dirk
Oosterlaan, Jaap
Faraone, Stephen V.
Franke, Barbara
Buitelaar, Jan K.
Hoekstra, Pieter J.
author_facet van der Meer, Dennis
Hartman, Catharina A.
Pruim, Raimon H. R.
Mennes, Maarten
Heslenfeld, Dirk
Oosterlaan, Jaap
Faraone, Stephen V.
Franke, Barbara
Buitelaar, Jan K.
Hoekstra, Pieter J.
author_sort van der Meer, Dennis
collection PubMed
description We recently reported that the serotonin transporter polymorphism 5-HTTLPR moderates the relation between stress exposure and attention-deficit/hyperactivity disorder (ADHD) severity. This gene-environment interaction (GxE) has been previously tied to the processing of emotional stimuli, which is increasingly recognized to be a key factor in ADHD-related impairment. The executive control and default mode brain networks play an important role in the regulation of emotion processing, and altered connectivity of these networks has also been associated with ADHD. We therefore investigated whether resting-state connectivity of either of these networks mediates the relation of 5-HTTLPR and stress exposure with ADHD severity. Resting-state functional magnetic resonance imaging, genetic, and stress exposure questionnaire data was available for 425 adolescents and young adults (average age 17.2 years). We found that 5-HTTLPR S-allele carriers showed a more negative relation between stress exposure and connectivity of the executive control network than L-allele homozygotes, specifically in the pre/postcentral gyrus, striatum, and frontal pole. In the default mode network, we found a positive association between the GxE and supramarginal gyrus connectivity. Connectivity of either network did not significantly mediate the effect of this GxE on ADHD. Opposite effects of stress exposure on connectivity in the executive and default mode networks may contribute to findings that stress exposure is associated with lowered cognitive control and heightened levels of rumination and worrying, for S-allele carriers but not L-allele homozygotes. When combined, these effects on connectivity of both networks may relate to the emotional problems seen in individuals with ADHD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11682-016-9633-3) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5653701
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-56537012017-11-01 The interaction between 5-HTTLPR and stress exposure influences connectivity of the executive control and default mode brain networks van der Meer, Dennis Hartman, Catharina A. Pruim, Raimon H. R. Mennes, Maarten Heslenfeld, Dirk Oosterlaan, Jaap Faraone, Stephen V. Franke, Barbara Buitelaar, Jan K. Hoekstra, Pieter J. Brain Imaging Behav Original Research We recently reported that the serotonin transporter polymorphism 5-HTTLPR moderates the relation between stress exposure and attention-deficit/hyperactivity disorder (ADHD) severity. This gene-environment interaction (GxE) has been previously tied to the processing of emotional stimuli, which is increasingly recognized to be a key factor in ADHD-related impairment. The executive control and default mode brain networks play an important role in the regulation of emotion processing, and altered connectivity of these networks has also been associated with ADHD. We therefore investigated whether resting-state connectivity of either of these networks mediates the relation of 5-HTTLPR and stress exposure with ADHD severity. Resting-state functional magnetic resonance imaging, genetic, and stress exposure questionnaire data was available for 425 adolescents and young adults (average age 17.2 years). We found that 5-HTTLPR S-allele carriers showed a more negative relation between stress exposure and connectivity of the executive control network than L-allele homozygotes, specifically in the pre/postcentral gyrus, striatum, and frontal pole. In the default mode network, we found a positive association between the GxE and supramarginal gyrus connectivity. Connectivity of either network did not significantly mediate the effect of this GxE on ADHD. Opposite effects of stress exposure on connectivity in the executive and default mode networks may contribute to findings that stress exposure is associated with lowered cognitive control and heightened levels of rumination and worrying, for S-allele carriers but not L-allele homozygotes. When combined, these effects on connectivity of both networks may relate to the emotional problems seen in individuals with ADHD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11682-016-9633-3) contains supplementary material, which is available to authorized users. Springer US 2016-10-13 2017 /pmc/articles/PMC5653701/ /pubmed/27738993 http://dx.doi.org/10.1007/s11682-016-9633-3 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
van der Meer, Dennis
Hartman, Catharina A.
Pruim, Raimon H. R.
Mennes, Maarten
Heslenfeld, Dirk
Oosterlaan, Jaap
Faraone, Stephen V.
Franke, Barbara
Buitelaar, Jan K.
Hoekstra, Pieter J.
The interaction between 5-HTTLPR and stress exposure influences connectivity of the executive control and default mode brain networks
title The interaction between 5-HTTLPR and stress exposure influences connectivity of the executive control and default mode brain networks
title_full The interaction between 5-HTTLPR and stress exposure influences connectivity of the executive control and default mode brain networks
title_fullStr The interaction between 5-HTTLPR and stress exposure influences connectivity of the executive control and default mode brain networks
title_full_unstemmed The interaction between 5-HTTLPR and stress exposure influences connectivity of the executive control and default mode brain networks
title_short The interaction between 5-HTTLPR and stress exposure influences connectivity of the executive control and default mode brain networks
title_sort interaction between 5-httlpr and stress exposure influences connectivity of the executive control and default mode brain networks
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653701/
https://www.ncbi.nlm.nih.gov/pubmed/27738993
http://dx.doi.org/10.1007/s11682-016-9633-3
work_keys_str_mv AT vandermeerdennis theinteractionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT hartmancatharinaa theinteractionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT pruimraimonhr theinteractionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT mennesmaarten theinteractionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT heslenfelddirk theinteractionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT oosterlaanjaap theinteractionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT faraonestephenv theinteractionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT frankebarbara theinteractionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT buitelaarjank theinteractionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT hoekstrapieterj theinteractionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT vandermeerdennis interactionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT hartmancatharinaa interactionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT pruimraimonhr interactionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT mennesmaarten interactionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT heslenfelddirk interactionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT oosterlaanjaap interactionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT faraonestephenv interactionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT frankebarbara interactionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT buitelaarjank interactionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks
AT hoekstrapieterj interactionbetween5httlprandstressexposureinfluencesconnectivityoftheexecutivecontrolanddefaultmodebrainnetworks