Traumatic stress, oxidative stress and post-traumatic stress disorder: neurodegeneration and the accelerated-aging hypothesis

Mol Psychiatry. 2014 Nov;19(11):1156-62. doi: 10.1038/mp.2014.111. Epub 2014 Sep 23.

Abstract

Post-traumatic stress disorder (PTSD) is associated with elevated risk for a variety of age-related diseases and neurodegeneration. In this paper, we review evidence relevant to the hypothesis that chronic PTSD constitutes a form of persistent life stress that potentiates oxidative stress (OXS) and accelerates cellular aging. We provide an overview of empirical studies that have examined the effects of psychological stress on OXS, discuss the stress-perpetuating characteristics of PTSD, and then identify mechanisms by which PTSD might promote OXS and accelerated aging. We review studies on OXS-related genes and the role that they may have in moderating the effects of PTSD on neural integrity and conclude with a discussion of directions for future research on antioxidant treatments and biomarkers of accelerated aging in PTSD.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Aging / genetics
  • Aging / physiology*
  • Animals
  • Chronic Disease
  • Humans
  • Nerve Degeneration / genetics
  • Nerve Degeneration / physiopathology*
  • Oxidative Stress / genetics
  • Oxidative Stress / physiology*
  • Stress Disorders, Post-Traumatic / genetics
  • Stress Disorders, Post-Traumatic / physiopathology*
  • Stress, Psychological / genetics
  • Stress, Psychological / physiopathology*