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Serotonin tranporter methylation and response to cognitive behaviour therapy in children with anxiety disorders

Anxiety disorders that are the most commonly occurring psychiatric disorders in childhood, are associated with a range of social and educational impairments and often continue into adulthood. Cognitive behaviour therapy (CBT) is an effective treatment option for the majority of cases, although up to...

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Autores principales: Roberts, S, Lester, K J, Hudson, J L, Rapee, R M, Creswell, C, Cooper, P J, Thirlwall, K J, Coleman, J R I, Breen, G, Wong, C C Y, Eley, T C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203012/
https://www.ncbi.nlm.nih.gov/pubmed/25226553
http://dx.doi.org/10.1038/tp.2014.83
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author Roberts, S
Lester, K J
Hudson, J L
Rapee, R M
Creswell, C
Cooper, P J
Thirlwall, K J
Coleman, J R I
Breen, G
Wong, C C Y
Eley, T C
author_facet Roberts, S
Lester, K J
Hudson, J L
Rapee, R M
Creswell, C
Cooper, P J
Thirlwall, K J
Coleman, J R I
Breen, G
Wong, C C Y
Eley, T C
author_sort Roberts, S
collection PubMed
description Anxiety disorders that are the most commonly occurring psychiatric disorders in childhood, are associated with a range of social and educational impairments and often continue into adulthood. Cognitive behaviour therapy (CBT) is an effective treatment option for the majority of cases, although up to 35–45% of children do not achieve remission. Recent research suggests that some genetic variants may be associated with a more beneficial response to psychological therapy. Epigenetic mechanisms such as DNA methylation work at the interface between genetic and environmental influences. Furthermore, epigenetic alterations at the serotonin transporter (SERT) promoter region have been associated with environmental influences such as stressful life experiences. In this study, we measured DNA methylation upstream of SERT in 116 children with an anxiety disorder, before and after receiving CBT. Change during treatment in percentage DNA methylation was significantly different in treatment responders vs nonresponders. This effect was driven by one CpG site in particular, at which responders increased in methylation, whereas nonresponders showed a decrease in DNA methylation. This is the first study to demonstrate differences in SERT methylation change in association with response to a purely psychological therapy. These findings confirm that biological changes occur alongside changes in symptomatology following a psychological therapy such as CBT.
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spelling pubmed-42030122014-11-06 Serotonin tranporter methylation and response to cognitive behaviour therapy in children with anxiety disorders Roberts, S Lester, K J Hudson, J L Rapee, R M Creswell, C Cooper, P J Thirlwall, K J Coleman, J R I Breen, G Wong, C C Y Eley, T C Transl Psychiatry Original Article Anxiety disorders that are the most commonly occurring psychiatric disorders in childhood, are associated with a range of social and educational impairments and often continue into adulthood. Cognitive behaviour therapy (CBT) is an effective treatment option for the majority of cases, although up to 35–45% of children do not achieve remission. Recent research suggests that some genetic variants may be associated with a more beneficial response to psychological therapy. Epigenetic mechanisms such as DNA methylation work at the interface between genetic and environmental influences. Furthermore, epigenetic alterations at the serotonin transporter (SERT) promoter region have been associated with environmental influences such as stressful life experiences. In this study, we measured DNA methylation upstream of SERT in 116 children with an anxiety disorder, before and after receiving CBT. Change during treatment in percentage DNA methylation was significantly different in treatment responders vs nonresponders. This effect was driven by one CpG site in particular, at which responders increased in methylation, whereas nonresponders showed a decrease in DNA methylation. This is the first study to demonstrate differences in SERT methylation change in association with response to a purely psychological therapy. These findings confirm that biological changes occur alongside changes in symptomatology following a psychological therapy such as CBT. Nature Publishing Group 2014-09 2014-09-16 /pmc/articles/PMC4203012/ /pubmed/25226553 http://dx.doi.org/10.1038/tp.2014.83 Text en Copyright © 2014 Macmillan Publishers Limited http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Original Article
Roberts, S
Lester, K J
Hudson, J L
Rapee, R M
Creswell, C
Cooper, P J
Thirlwall, K J
Coleman, J R I
Breen, G
Wong, C C Y
Eley, T C
Serotonin tranporter methylation and response to cognitive behaviour therapy in children with anxiety disorders
title Serotonin tranporter methylation and response to cognitive behaviour therapy in children with anxiety disorders
title_full Serotonin tranporter methylation and response to cognitive behaviour therapy in children with anxiety disorders
title_fullStr Serotonin tranporter methylation and response to cognitive behaviour therapy in children with anxiety disorders
title_full_unstemmed Serotonin tranporter methylation and response to cognitive behaviour therapy in children with anxiety disorders
title_short Serotonin tranporter methylation and response to cognitive behaviour therapy in children with anxiety disorders
title_sort serotonin tranporter methylation and response to cognitive behaviour therapy in children with anxiety disorders
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203012/
https://www.ncbi.nlm.nih.gov/pubmed/25226553
http://dx.doi.org/10.1038/tp.2014.83
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