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Treatment-associated mRNA co-expression changes in monocytes of patients with posttraumatic stress disorder
PTSD is a prevalent mental disorder that results from exposure to extreme and stressful life events and comes at high costs for both the individual and society. Therapeutic treatment presents the best way to deal with PTSD-the mechanisms underlying change after treatment, however, remain poorly unde...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10326517/ https://www.ncbi.nlm.nih.gov/pubmed/37426106 http://dx.doi.org/10.3389/fpsyt.2023.1181321 |
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author | Kumsta, Robert Zang, Johannes C. S. Hummel, Elisabeth M. Müller, Svenja Moser, Dirk A. Herpertz, Stephan Kessler, Henrik |
author_facet | Kumsta, Robert Zang, Johannes C. S. Hummel, Elisabeth M. Müller, Svenja Moser, Dirk A. Herpertz, Stephan Kessler, Henrik |
author_sort | Kumsta, Robert |
collection | PubMed |
description | PTSD is a prevalent mental disorder that results from exposure to extreme and stressful life events and comes at high costs for both the individual and society. Therapeutic treatment presents the best way to deal with PTSD-the mechanisms underlying change after treatment, however, remain poorly understood. While stress and immune associated gene expression changes have been associated with PTSD development, studies investigating treatment effects at the molecular level so far tended to focus on DNA methylation. Here we use gene-network analysis on whole-transcriptome RNA-Seq data isolated from CD14(+) monocytes of female PTSD patients (N = 51) to study pre-treatment signatures of therapy response and therapy-related changes at the level of gene expression. Patients who exhibited significant symptom improvement after therapy showed higher baseline expression in two modules involved in inflammatory processes (including notable examples IL1R2 and FKBP5) and blood coagulation. After therapy, expression of an inflammatory module was increased, and expression of a wound healing module was decreased. This supports findings reporting an association between PTSD and dysregulations of the inflammatory and the hemostatic system and mark both as potentially treatment sensitive. |
format | Online Article Text |
id | pubmed-10326517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103265172023-07-08 Treatment-associated mRNA co-expression changes in monocytes of patients with posttraumatic stress disorder Kumsta, Robert Zang, Johannes C. S. Hummel, Elisabeth M. Müller, Svenja Moser, Dirk A. Herpertz, Stephan Kessler, Henrik Front Psychiatry Psychiatry PTSD is a prevalent mental disorder that results from exposure to extreme and stressful life events and comes at high costs for both the individual and society. Therapeutic treatment presents the best way to deal with PTSD-the mechanisms underlying change after treatment, however, remain poorly understood. While stress and immune associated gene expression changes have been associated with PTSD development, studies investigating treatment effects at the molecular level so far tended to focus on DNA methylation. Here we use gene-network analysis on whole-transcriptome RNA-Seq data isolated from CD14(+) monocytes of female PTSD patients (N = 51) to study pre-treatment signatures of therapy response and therapy-related changes at the level of gene expression. Patients who exhibited significant symptom improvement after therapy showed higher baseline expression in two modules involved in inflammatory processes (including notable examples IL1R2 and FKBP5) and blood coagulation. After therapy, expression of an inflammatory module was increased, and expression of a wound healing module was decreased. This supports findings reporting an association between PTSD and dysregulations of the inflammatory and the hemostatic system and mark both as potentially treatment sensitive. Frontiers Media S.A. 2023-06-23 /pmc/articles/PMC10326517/ /pubmed/37426106 http://dx.doi.org/10.3389/fpsyt.2023.1181321 Text en Copyright © 2023 Kumsta, Zang, Hummel, Müller, Moser, Herpertz and Kessler. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Psychiatry Kumsta, Robert Zang, Johannes C. S. Hummel, Elisabeth M. Müller, Svenja Moser, Dirk A. Herpertz, Stephan Kessler, Henrik Treatment-associated mRNA co-expression changes in monocytes of patients with posttraumatic stress disorder |
title | Treatment-associated mRNA co-expression changes in monocytes of patients with posttraumatic stress disorder |
title_full | Treatment-associated mRNA co-expression changes in monocytes of patients with posttraumatic stress disorder |
title_fullStr | Treatment-associated mRNA co-expression changes in monocytes of patients with posttraumatic stress disorder |
title_full_unstemmed | Treatment-associated mRNA co-expression changes in monocytes of patients with posttraumatic stress disorder |
title_short | Treatment-associated mRNA co-expression changes in monocytes of patients with posttraumatic stress disorder |
title_sort | treatment-associated mrna co-expression changes in monocytes of patients with posttraumatic stress disorder |
topic | Psychiatry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10326517/ https://www.ncbi.nlm.nih.gov/pubmed/37426106 http://dx.doi.org/10.3389/fpsyt.2023.1181321 |
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