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Epigenome-wide meta-analysis of PTSD across 10 military and civilian cohorts identifies methylation changes in AHRR
Epigenetic differences may help to distinguish between PTSD cases and trauma-exposed controls. Here, we describe the results of the largest DNA methylation meta-analysis of PTSD to date. Ten cohorts, military and civilian, contribute blood-derived DNA methylation data from 1,896 PTSD cases and traum...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7686485/ https://www.ncbi.nlm.nih.gov/pubmed/33235198 http://dx.doi.org/10.1038/s41467-020-19615-x |
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author | Smith, Alicia K. Ratanatharathorn, Andrew Maihofer, Adam X. Naviaux, Robert K. Aiello, Allison E. Amstadter, Ananda B. Ashley-Koch, Allison E. Baker, Dewleen G. Beckham, Jean C. Boks, Marco P. Bromet, Evelyn Dennis, Michelle Galea, Sandro Garrett, Melanie E. Geuze, Elbert Guffanti, Guia Hauser, Michael A. Katrinli, Seyma Kilaru, Varun Kessler, Ronald C. Kimbrel, Nathan A. Koenen, Karestan C. Kuan, Pei-Fen Li, Kefeng Logue, Mark W. Lori, Adriana Luft, Benjamin J. Miller, Mark W. Naviaux, Jane C. Nugent, Nicole R. Qin, Xuejun Ressler, Kerry J. Risbrough, Victoria B. Rutten, Bart P. F. Stein, Murray B. Ursano, Robert J. Vermetten, Eric Vinkers, Christiaan H. Wang, Lin Youssef, Nagy A. Uddin, Monica Nievergelt, Caroline M. |
author_facet | Smith, Alicia K. Ratanatharathorn, Andrew Maihofer, Adam X. Naviaux, Robert K. Aiello, Allison E. Amstadter, Ananda B. Ashley-Koch, Allison E. Baker, Dewleen G. Beckham, Jean C. Boks, Marco P. Bromet, Evelyn Dennis, Michelle Galea, Sandro Garrett, Melanie E. Geuze, Elbert Guffanti, Guia Hauser, Michael A. Katrinli, Seyma Kilaru, Varun Kessler, Ronald C. Kimbrel, Nathan A. Koenen, Karestan C. Kuan, Pei-Fen Li, Kefeng Logue, Mark W. Lori, Adriana Luft, Benjamin J. Miller, Mark W. Naviaux, Jane C. Nugent, Nicole R. Qin, Xuejun Ressler, Kerry J. Risbrough, Victoria B. Rutten, Bart P. F. Stein, Murray B. Ursano, Robert J. Vermetten, Eric Vinkers, Christiaan H. Wang, Lin Youssef, Nagy A. Uddin, Monica Nievergelt, Caroline M. |
author_sort | Smith, Alicia K. |
collection | PubMed |
description | Epigenetic differences may help to distinguish between PTSD cases and trauma-exposed controls. Here, we describe the results of the largest DNA methylation meta-analysis of PTSD to date. Ten cohorts, military and civilian, contribute blood-derived DNA methylation data from 1,896 PTSD cases and trauma-exposed controls. Four CpG sites within the aryl-hydrocarbon receptor repressor (AHRR) associate with PTSD after adjustment for multiple comparisons, with lower DNA methylation in PTSD cases relative to controls. Although AHRR methylation is known to associate with smoking, the AHRR association with PTSD is most pronounced in non-smokers, suggesting the result was independent of smoking status. Evaluation of metabolomics data reveals that AHRR methylation associated with kynurenine levels, which are lower among subjects with PTSD. This study supports epigenetic differences in those with PTSD and suggests a role for decreased kynurenine as a contributor to immune dysregulation in PTSD. |
format | Online Article Text |
id | pubmed-7686485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76864852020-12-03 Epigenome-wide meta-analysis of PTSD across 10 military and civilian cohorts identifies methylation changes in AHRR Smith, Alicia K. Ratanatharathorn, Andrew Maihofer, Adam X. Naviaux, Robert K. Aiello, Allison E. Amstadter, Ananda B. Ashley-Koch, Allison E. Baker, Dewleen G. Beckham, Jean C. Boks, Marco P. Bromet, Evelyn Dennis, Michelle Galea, Sandro Garrett, Melanie E. Geuze, Elbert Guffanti, Guia Hauser, Michael A. Katrinli, Seyma Kilaru, Varun Kessler, Ronald C. Kimbrel, Nathan A. Koenen, Karestan C. Kuan, Pei-Fen Li, Kefeng Logue, Mark W. Lori, Adriana Luft, Benjamin J. Miller, Mark W. Naviaux, Jane C. Nugent, Nicole R. Qin, Xuejun Ressler, Kerry J. Risbrough, Victoria B. Rutten, Bart P. F. Stein, Murray B. Ursano, Robert J. Vermetten, Eric Vinkers, Christiaan H. Wang, Lin Youssef, Nagy A. Uddin, Monica Nievergelt, Caroline M. Nat Commun Article Epigenetic differences may help to distinguish between PTSD cases and trauma-exposed controls. Here, we describe the results of the largest DNA methylation meta-analysis of PTSD to date. Ten cohorts, military and civilian, contribute blood-derived DNA methylation data from 1,896 PTSD cases and trauma-exposed controls. Four CpG sites within the aryl-hydrocarbon receptor repressor (AHRR) associate with PTSD after adjustment for multiple comparisons, with lower DNA methylation in PTSD cases relative to controls. Although AHRR methylation is known to associate with smoking, the AHRR association with PTSD is most pronounced in non-smokers, suggesting the result was independent of smoking status. Evaluation of metabolomics data reveals that AHRR methylation associated with kynurenine levels, which are lower among subjects with PTSD. This study supports epigenetic differences in those with PTSD and suggests a role for decreased kynurenine as a contributor to immune dysregulation in PTSD. Nature Publishing Group UK 2020-11-24 /pmc/articles/PMC7686485/ /pubmed/33235198 http://dx.doi.org/10.1038/s41467-020-19615-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Smith, Alicia K. Ratanatharathorn, Andrew Maihofer, Adam X. Naviaux, Robert K. Aiello, Allison E. Amstadter, Ananda B. Ashley-Koch, Allison E. Baker, Dewleen G. Beckham, Jean C. Boks, Marco P. Bromet, Evelyn Dennis, Michelle Galea, Sandro Garrett, Melanie E. Geuze, Elbert Guffanti, Guia Hauser, Michael A. Katrinli, Seyma Kilaru, Varun Kessler, Ronald C. Kimbrel, Nathan A. Koenen, Karestan C. Kuan, Pei-Fen Li, Kefeng Logue, Mark W. Lori, Adriana Luft, Benjamin J. Miller, Mark W. Naviaux, Jane C. Nugent, Nicole R. Qin, Xuejun Ressler, Kerry J. Risbrough, Victoria B. Rutten, Bart P. F. Stein, Murray B. Ursano, Robert J. Vermetten, Eric Vinkers, Christiaan H. Wang, Lin Youssef, Nagy A. Uddin, Monica Nievergelt, Caroline M. Epigenome-wide meta-analysis of PTSD across 10 military and civilian cohorts identifies methylation changes in AHRR |
title | Epigenome-wide meta-analysis of PTSD across 10 military and civilian cohorts identifies methylation changes in AHRR |
title_full | Epigenome-wide meta-analysis of PTSD across 10 military and civilian cohorts identifies methylation changes in AHRR |
title_fullStr | Epigenome-wide meta-analysis of PTSD across 10 military and civilian cohorts identifies methylation changes in AHRR |
title_full_unstemmed | Epigenome-wide meta-analysis of PTSD across 10 military and civilian cohorts identifies methylation changes in AHRR |
title_short | Epigenome-wide meta-analysis of PTSD across 10 military and civilian cohorts identifies methylation changes in AHRR |
title_sort | epigenome-wide meta-analysis of ptsd across 10 military and civilian cohorts identifies methylation changes in ahrr |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7686485/ https://www.ncbi.nlm.nih.gov/pubmed/33235198 http://dx.doi.org/10.1038/s41467-020-19615-x |
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