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No association between war-related trauma or PTSD symptom severity and epigenome-wide DNA methylation in Burundian refugees
Background: War-related trauma is associated with varying posttraumatic stress disorder (PTSD) prevalence rates in refugees. In PTSD development, differential DNA methylation (DNAm) levels associated with trauma exposure might be involved in risk versus resilience processes. Studies investigating DN...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324453/ https://www.ncbi.nlm.nih.gov/pubmed/37405801 http://dx.doi.org/10.1080/20008066.2023.2228155 |
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author | Mattonet, Katharina Scharpf, Florian Block, Katrin Kumsta, Robert Hecker, Tobias |
author_facet | Mattonet, Katharina Scharpf, Florian Block, Katrin Kumsta, Robert Hecker, Tobias |
author_sort | Mattonet, Katharina |
collection | PubMed |
description | Background: War-related trauma is associated with varying posttraumatic stress disorder (PTSD) prevalence rates in refugees. In PTSD development, differential DNA methylation (DNAm) levels associated with trauma exposure might be involved in risk versus resilience processes. Studies investigating DNAm profiles related to trauma exposure and PTSD among refugees remain sparse. Objective: The present epigenome-wide association study investigated associations between war-related trauma, PTSD, and altered DNAm patterns in Burundian refugee families with 110 children and their 207 female and male caregivers. Method: War-related trauma load and PTSD symptom severity were assessed in structured clinical interviews with standardised instruments. Epigenome-wide DNAm levels were quantified from buccal epithelia using the Illumina EPIC beadchip. Results: Controlling for biological confounders, no significant epigenome-wide DNAm alterations associated with trauma exposure or PTSD were identified in children or caregivers (FDRs > .05). Co-methylated positions derived as modules from weighted gene correlation network analyses were not significantly associated with either war-related trauma experience in children or caregivers or with PTSD. Conclusions: These results do not provide evidence for altered DNAm patterns associated with exposure to war-related trauma or PTSD. |
format | Online Article Text |
id | pubmed-10324453 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-103244532023-07-07 No association between war-related trauma or PTSD symptom severity and epigenome-wide DNA methylation in Burundian refugees Mattonet, Katharina Scharpf, Florian Block, Katrin Kumsta, Robert Hecker, Tobias Eur J Psychotraumatol Basic Research Article Background: War-related trauma is associated with varying posttraumatic stress disorder (PTSD) prevalence rates in refugees. In PTSD development, differential DNA methylation (DNAm) levels associated with trauma exposure might be involved in risk versus resilience processes. Studies investigating DNAm profiles related to trauma exposure and PTSD among refugees remain sparse. Objective: The present epigenome-wide association study investigated associations between war-related trauma, PTSD, and altered DNAm patterns in Burundian refugee families with 110 children and their 207 female and male caregivers. Method: War-related trauma load and PTSD symptom severity were assessed in structured clinical interviews with standardised instruments. Epigenome-wide DNAm levels were quantified from buccal epithelia using the Illumina EPIC beadchip. Results: Controlling for biological confounders, no significant epigenome-wide DNAm alterations associated with trauma exposure or PTSD were identified in children or caregivers (FDRs > .05). Co-methylated positions derived as modules from weighted gene correlation network analyses were not significantly associated with either war-related trauma experience in children or caregivers or with PTSD. Conclusions: These results do not provide evidence for altered DNAm patterns associated with exposure to war-related trauma or PTSD. Taylor & Francis 2023-07-05 /pmc/articles/PMC10324453/ /pubmed/37405801 http://dx.doi.org/10.1080/20008066.2023.2228155 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Basic Research Article Mattonet, Katharina Scharpf, Florian Block, Katrin Kumsta, Robert Hecker, Tobias No association between war-related trauma or PTSD symptom severity and epigenome-wide DNA methylation in Burundian refugees |
title | No association between war-related trauma or PTSD symptom severity and epigenome-wide DNA methylation in Burundian refugees |
title_full | No association between war-related trauma or PTSD symptom severity and epigenome-wide DNA methylation in Burundian refugees |
title_fullStr | No association between war-related trauma or PTSD symptom severity and epigenome-wide DNA methylation in Burundian refugees |
title_full_unstemmed | No association between war-related trauma or PTSD symptom severity and epigenome-wide DNA methylation in Burundian refugees |
title_short | No association between war-related trauma or PTSD symptom severity and epigenome-wide DNA methylation in Burundian refugees |
title_sort | no association between war-related trauma or ptsd symptom severity and epigenome-wide dna methylation in burundian refugees |
topic | Basic Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10324453/ https://www.ncbi.nlm.nih.gov/pubmed/37405801 http://dx.doi.org/10.1080/20008066.2023.2228155 |
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