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HPA AXIS RELATED GENES AND RESPONSE TO PSYCHOLOGICAL THERAPIES: GENETICS AND EPIGENETICS
BACKGROUND: Hypothalamic–pituitary–adrenal (HPA) axis functioning has been implicated in the development of stress‐related psychiatric diagnoses and response to adverse life experiences. This study aimed to investigate the association between genetic and epigenetics in HPA axis and response to cogni...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982063/ https://www.ncbi.nlm.nih.gov/pubmed/26647360 http://dx.doi.org/10.1002/da.22430 |
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author | Roberts, Susanna Keers, Robert Lester, Kathryn J Coleman, Jonathan R. I. Breen, Gerome Arendt, Kristian Blatter‐Meunier, Judith Cooper, Peter Creswell, Cathy Fjermestad, Krister Havik, Odd E. Herren, Chantal Hogendoorn, Sanne M. Hudson, Jennifer L. Krause, Karen Lyneham, Heidi J. Morris, Talia Nauta, Maaike Rapee, Ronald M. Rey, Yasmin Schneider, Silvia Schneider, Sophie C. Silverman, Wendy K. Thastum, Mikael Thirlwall, Kerstin Waite, Polly Eley, Thalia C. Wong, Chloe C. Y. |
author_facet | Roberts, Susanna Keers, Robert Lester, Kathryn J Coleman, Jonathan R. I. Breen, Gerome Arendt, Kristian Blatter‐Meunier, Judith Cooper, Peter Creswell, Cathy Fjermestad, Krister Havik, Odd E. Herren, Chantal Hogendoorn, Sanne M. Hudson, Jennifer L. Krause, Karen Lyneham, Heidi J. Morris, Talia Nauta, Maaike Rapee, Ronald M. Rey, Yasmin Schneider, Silvia Schneider, Sophie C. Silverman, Wendy K. Thastum, Mikael Thirlwall, Kerstin Waite, Polly Eley, Thalia C. Wong, Chloe C. Y. |
author_sort | Roberts, Susanna |
collection | PubMed |
description | BACKGROUND: Hypothalamic–pituitary–adrenal (HPA) axis functioning has been implicated in the development of stress‐related psychiatric diagnoses and response to adverse life experiences. This study aimed to investigate the association between genetic and epigenetics in HPA axis and response to cognitive behavior therapy (CBT). METHODS: Children with anxiety disorders were recruited into the Genes for Treatment project (GxT, N = 1,152). Polymorphisms of FKBP5 and GR were analyzed for association with response to CBT. Percentage DNA methylation at the FKBP5 and GR promoter regions was measured before and after CBT in a subset (n = 98). Linear mixed effect models were used to investigate the relationship between genotype, DNA methylation, and change in primary anxiety disorder severity (treatment response). RESULTS: Treatment response was not associated with FKBP5 and GR polymorphisms, or pretreatment percentage DNA methylation. However, change in FKBP5 DNA methylation was nominally significantly associated with treatment response. Participants who demonstrated the greatest reduction in severity decreased in percentage DNA methylation during treatment, whereas those with little/no reduction in severity increased in percentage DNA methylation. This effect was driven by those with one or more FKBP5 risk alleles, with no association seen in those with no FKBP5 risk alleles. No significant association was found between GR methylation and response. CONCLUSIONS: Allele‐specific change in FKBP5 methylation was associated with treatment response. This is the largest study to date investigating the role of HPA axis related genes in response to a psychological therapy. Furthermore, this is the first study to demonstrate that DNA methylation changes may be associated with response to psychological therapies in a genotype‐dependent manner. |
format | Online Article Text |
id | pubmed-4982063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-49820632016-08-26 HPA AXIS RELATED GENES AND RESPONSE TO PSYCHOLOGICAL THERAPIES: GENETICS AND EPIGENETICS Roberts, Susanna Keers, Robert Lester, Kathryn J Coleman, Jonathan R. I. Breen, Gerome Arendt, Kristian Blatter‐Meunier, Judith Cooper, Peter Creswell, Cathy Fjermestad, Krister Havik, Odd E. Herren, Chantal Hogendoorn, Sanne M. Hudson, Jennifer L. Krause, Karen Lyneham, Heidi J. Morris, Talia Nauta, Maaike Rapee, Ronald M. Rey, Yasmin Schneider, Silvia Schneider, Sophie C. Silverman, Wendy K. Thastum, Mikael Thirlwall, Kerstin Waite, Polly Eley, Thalia C. Wong, Chloe C. Y. Depress Anxiety Research Article BACKGROUND: Hypothalamic–pituitary–adrenal (HPA) axis functioning has been implicated in the development of stress‐related psychiatric diagnoses and response to adverse life experiences. This study aimed to investigate the association between genetic and epigenetics in HPA axis and response to cognitive behavior therapy (CBT). METHODS: Children with anxiety disorders were recruited into the Genes for Treatment project (GxT, N = 1,152). Polymorphisms of FKBP5 and GR were analyzed for association with response to CBT. Percentage DNA methylation at the FKBP5 and GR promoter regions was measured before and after CBT in a subset (n = 98). Linear mixed effect models were used to investigate the relationship between genotype, DNA methylation, and change in primary anxiety disorder severity (treatment response). RESULTS: Treatment response was not associated with FKBP5 and GR polymorphisms, or pretreatment percentage DNA methylation. However, change in FKBP5 DNA methylation was nominally significantly associated with treatment response. Participants who demonstrated the greatest reduction in severity decreased in percentage DNA methylation during treatment, whereas those with little/no reduction in severity increased in percentage DNA methylation. This effect was driven by those with one or more FKBP5 risk alleles, with no association seen in those with no FKBP5 risk alleles. No significant association was found between GR methylation and response. CONCLUSIONS: Allele‐specific change in FKBP5 methylation was associated with treatment response. This is the largest study to date investigating the role of HPA axis related genes in response to a psychological therapy. Furthermore, this is the first study to demonstrate that DNA methylation changes may be associated with response to psychological therapies in a genotype‐dependent manner. John Wiley and Sons Inc. 2015-12 2015-10-07 /pmc/articles/PMC4982063/ /pubmed/26647360 http://dx.doi.org/10.1002/da.22430 Text en © 2015 The Authors. Depression and Anxiety published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Roberts, Susanna Keers, Robert Lester, Kathryn J Coleman, Jonathan R. I. Breen, Gerome Arendt, Kristian Blatter‐Meunier, Judith Cooper, Peter Creswell, Cathy Fjermestad, Krister Havik, Odd E. Herren, Chantal Hogendoorn, Sanne M. Hudson, Jennifer L. Krause, Karen Lyneham, Heidi J. Morris, Talia Nauta, Maaike Rapee, Ronald M. Rey, Yasmin Schneider, Silvia Schneider, Sophie C. Silverman, Wendy K. Thastum, Mikael Thirlwall, Kerstin Waite, Polly Eley, Thalia C. Wong, Chloe C. Y. HPA AXIS RELATED GENES AND RESPONSE TO PSYCHOLOGICAL THERAPIES: GENETICS AND EPIGENETICS |
title | HPA AXIS RELATED GENES AND RESPONSE TO PSYCHOLOGICAL THERAPIES: GENETICS AND EPIGENETICS |
title_full | HPA AXIS RELATED GENES AND RESPONSE TO PSYCHOLOGICAL THERAPIES: GENETICS AND EPIGENETICS |
title_fullStr | HPA AXIS RELATED GENES AND RESPONSE TO PSYCHOLOGICAL THERAPIES: GENETICS AND EPIGENETICS |
title_full_unstemmed | HPA AXIS RELATED GENES AND RESPONSE TO PSYCHOLOGICAL THERAPIES: GENETICS AND EPIGENETICS |
title_short | HPA AXIS RELATED GENES AND RESPONSE TO PSYCHOLOGICAL THERAPIES: GENETICS AND EPIGENETICS |
title_sort | hpa axis related genes and response to psychological therapies: genetics and epigenetics |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4982063/ https://www.ncbi.nlm.nih.gov/pubmed/26647360 http://dx.doi.org/10.1002/da.22430 |
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