Accelerated DNA methylation aging and increased resilience in veterans: The biological cost for soldiering on

Accelerated epigenetic aging, the difference between the DNA methylation-predicted age (DNAm age) and the chronological age, is associated with a myriad of diseases. This study investigates the relationship between epigenetic aging and risk and protective factors of PTSD. Genome-wide DNA methylation...

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Main Authors: Divya Mehta, Dagmar Bruenig, Bruce Lawford, Wendy Harvey, Tania Carrillo-Roa, Charles P. Morris, Tanja Jovanovic, Ross McD. Young, Elisabeth B. Binder, Joanne Voisey
Format: Article
Language:English
Published: Elsevier 2018-02-01
Series:Neurobiology of Stress
Online Access:http://www.sciencedirect.com/science/article/pii/S2352289517300528
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author Divya Mehta
Dagmar Bruenig
Bruce Lawford
Wendy Harvey
Tania Carrillo-Roa
Charles P. Morris
Tanja Jovanovic
Ross McD. Young
Elisabeth B. Binder
Joanne Voisey
spellingShingle Divya Mehta
Dagmar Bruenig
Bruce Lawford
Wendy Harvey
Tania Carrillo-Roa
Charles P. Morris
Tanja Jovanovic
Ross McD. Young
Elisabeth B. Binder
Joanne Voisey
Accelerated DNA methylation aging and increased resilience in veterans: The biological cost for soldiering on
Neurobiology of Stress
author_facet Divya Mehta
Dagmar Bruenig
Bruce Lawford
Wendy Harvey
Tania Carrillo-Roa
Charles P. Morris
Tanja Jovanovic
Ross McD. Young
Elisabeth B. Binder
Joanne Voisey
author_sort Divya Mehta
title Accelerated DNA methylation aging and increased resilience in veterans: The biological cost for soldiering on
title_short Accelerated DNA methylation aging and increased resilience in veterans: The biological cost for soldiering on
title_full Accelerated DNA methylation aging and increased resilience in veterans: The biological cost for soldiering on
title_fullStr Accelerated DNA methylation aging and increased resilience in veterans: The biological cost for soldiering on
title_full_unstemmed Accelerated DNA methylation aging and increased resilience in veterans: The biological cost for soldiering on
title_sort accelerated dna methylation aging and increased resilience in veterans: the biological cost for soldiering on
publisher Elsevier
series Neurobiology of Stress
issn 2352-2895
publishDate 2018-02-01
description Accelerated epigenetic aging, the difference between the DNA methylation-predicted age (DNAm age) and the chronological age, is associated with a myriad of diseases. This study investigates the relationship between epigenetic aging and risk and protective factors of PTSD. Genome-wide DNA methylation analysis was performed in 211 individuals including combat-exposed Australian veterans (discovery cohort, n = 96 males) and trauma-exposed civilian males from the Grady Trauma Project (replication cohort, n = 115 males). Primary measures included the Clinician Administered PTSD Scale for DSM-5 and the Connor-Davidson Resilience Scale (CD-RISC). DNAm age prediction was performed using the validated epigenetic clock calculator. Veterans with PTSD had increased PTSD symptom severity (P-value = 3.75 × 10−34) and lower CD-RISC scores (P-value = 7.5 × 10−8) than veterans without PTSD. DNAm age was significantly correlated with the chronological age (P-value = 3.3 × 10−6), but DNAm age acceleration was not different between the PTSD and non-PTSD groups (P-value = 0.24). Evaluating potential protective factors, we found that DNAm age acceleration was significantly associated with CD-RISC resilience scores in veterans with PTSD, these results remained significant after multiple testing correction (P-value = 0.023; r = 0.32). This finding was also replicated in an independent trauma-exposed civilian cohort (P-value = 0.02; r = 0.23). Post-hoc factor analyses revealed that this association was likely driven by “self-efficacy” items within the CD-RISC (P-value = 0.015; r = 0.35). These results suggest that among individuals already suffering from PTSD, some aspects of increased resilience might come at a biological cost. Keywords: Epigenetic aging, Biomarkers, Veterans, Stress, PTSD, Resilience
url http://www.sciencedirect.com/science/article/pii/S2352289517300528
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spelling doaj-e68ba739b7e944e4b6c1e87c26fdabf72020-11-24T22:49:04ZengElsevierNeurobiology of Stress2352-28952018-02-018112119Accelerated DNA methylation aging and increased resilience in veterans: The biological cost for soldiering onDivya Mehta0Dagmar Bruenig1Bruce Lawford2Wendy Harvey3Tania Carrillo-Roa4Charles P. Morris5Tanja Jovanovic6Ross McD. Young7Elisabeth B. Binder8Joanne Voisey9School of Psychology and Counselling, Faculty of Health, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, Queensland 4059, Australia; Corresponding author. School of Psychology and Counselling, Faculty of Health Institute of Health and Biomedical Innovation (IHBI), 60 Musk Avenue, Queensland University of Technology, Kelvin Grove, Queensland, 4059, Australia.School of Biomedical Sciences, Faculty of Health, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, Queensland 4059, Australia; Gallipoli Medical Research Institute, Greenslopes Private Hospital, Newdegate Street, Greenslopes, QLD 4120, AustraliaSchool of Biomedical Sciences, Faculty of Health, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, Queensland 4059, AustraliaGallipoli Medical Research Institute, Greenslopes Private Hospital, Newdegate Street, Greenslopes, QLD 4120, AustraliaDepartment of Translational Research in Psychiatry, Max Planck Institute of Psychiatry, Munich, 80804, GermanySchool of Biomedical Sciences, Faculty of Health, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, Queensland 4059, AustraliaDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA 30322, USASchool of Psychology and Counselling, Faculty of Health, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, Queensland 4059, Australia; Gallipoli Medical Research Institute, Greenslopes Private Hospital, Newdegate Street, Greenslopes, QLD 4120, AustraliaDepartment of Translational Research in Psychiatry, Max Planck Institute of Psychiatry, Munich, 80804, Germany; Department of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA 30322, USASchool of Biomedical Sciences, Faculty of Health, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, Queensland 4059, AustraliaAccelerated epigenetic aging, the difference between the DNA methylation-predicted age (DNAm age) and the chronological age, is associated with a myriad of diseases. This study investigates the relationship between epigenetic aging and risk and protective factors of PTSD. Genome-wide DNA methylation analysis was performed in 211 individuals including combat-exposed Australian veterans (discovery cohort, n = 96 males) and trauma-exposed civilian males from the Grady Trauma Project (replication cohort, n = 115 males). Primary measures included the Clinician Administered PTSD Scale for DSM-5 and the Connor-Davidson Resilience Scale (CD-RISC). DNAm age prediction was performed using the validated epigenetic clock calculator. Veterans with PTSD had increased PTSD symptom severity (P-value = 3.75 × 10−34) and lower CD-RISC scores (P-value = 7.5 × 10−8) than veterans without PTSD. DNAm age was significantly correlated with the chronological age (P-value = 3.3 × 10−6), but DNAm age acceleration was not different between the PTSD and non-PTSD groups (P-value = 0.24). Evaluating potential protective factors, we found that DNAm age acceleration was significantly associated with CD-RISC resilience scores in veterans with PTSD, these results remained significant after multiple testing correction (P-value = 0.023; r = 0.32). This finding was also replicated in an independent trauma-exposed civilian cohort (P-value = 0.02; r = 0.23). Post-hoc factor analyses revealed that this association was likely driven by “self-efficacy” items within the CD-RISC (P-value = 0.015; r = 0.35). These results suggest that among individuals already suffering from PTSD, some aspects of increased resilience might come at a biological cost. Keywords: Epigenetic aging, Biomarkers, Veterans, Stress, PTSD, Resiliencehttp://www.sciencedirect.com/science/article/pii/S2352289517300528