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Author Notes:

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. divya.mehta@qut.edu.au (D. Mehta).

The authors thank the Gallipoli Medical Research Foundation for their support, especially Miriam Dwyer and Dr Sarah McLeay for their project management support.

The authors would also like to acknowledge Dr Madeline Romaniuk for psychological expertise and Dr John Gibson and the team at the Keith Payne Unit, and the staff and investigators at Greenslopes Private Hospital for their valuable contribution to the study.

All authors extend their gratitude to the study participants for their generous provision of data and time.

The Gallipoli Medical Research Foundation wishes to thank the RSL QLD for their generous donation, and Sullivan Nicolaides Pathology and Queensland X-Ray for their in-kind support.

The authors thank QUT and IHBI for financial and administrative support.

All authors report no potential conflicts of interest.

Subjects:

Research Funding:

The PTSD Initiative was funded by the Queensland Branch of the Returned & Services League of Australia (RSL QLD).

Divya Mehta was funded via the QUT Vice Chancellors Research Fellowship.

Keywords:

  • Biomarkers
  • Epigenetic aging
  • PTSD
  • Resilience
  • Stress
  • Veterans

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

Tools:

Journal Title:

Neurobiology of Stress

Volume:

Volume 8

Publisher:

, Pages 112-119

Type of Work:

Article | Final Publisher PDF

Abstract:

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.

Copyright information:

© 2018 The Authors

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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