4.5 Article

The role of acute cortisol and DHEAS in predicting acute and chronic PTSD symptoms

期刊

PSYCHONEUROENDOCRINOLOGY
卷 45, 期 -, 页码 179-186

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.psyneuen.2014.04.001

关键词

Posttraumatic stress disorder; Cortisol; DHEAS; Traumatic injury; Predictors; Prospective study

资金

  1. Netherlands Organization for Health Research and Development (ZonMw) [62300038]
  2. Stichting Achmea Slachtoffer en Samenleving (SASS), Aid to Victims, Zeist, The Netherlands

向作者/读者索取更多资源

Background: Decreased activation of the hypothalamus pituitary adrenal (HPA) axis in response to stress is suspected to be a vulnerability factor for posttraumatic stress disorder (PTSD). Previous studies showed inconsistent findings regarding the role of cortisol in predicting PTSD. In addition, no prospective studies have examined the role of dehydroepiandrosterone (DHEA), or its sulfate form DHEAS, and the cortisol-to-DHEA(S) ratio in predicting PTSD. In this study, we tested whether acute plasma cortisol, DHEAS and the cortisol-to-DHEAS ratio predicted PTSD symptoms at 6 weeks and 6 months post-trauma. Methods: Blood samples of 397 adult level-1 trauma center patients, taken at the trauma resuscitation room within hours after the injury, were analyzed for cortisol and DHEAS levels. PTSD symptoms were assessed at 6 weeks and 6 months post-trauma with the Clinician Administered PTSD Scale. Results: Multivariate linear regression analyses showed that lower cortisol predicted PTSD symptoms at both 6 weeks and 6 months, controlling for age, gender, time of blood sampling, injury, trauma history, and admission to intensive care. Higher DHEAS and a smaller cortisol-toDHEAS ratio predicted PTSD symptoms at 6 weeks, but not after controlling for the same variables, and not at 6 months. Conclusions: Our study provides important new evidence on the crucial role of the HPA-axis in response to trauma by showing that acute cortisol and DHEAS levels predict PTSD symptoms in survivors of recent trauma. (c) 2014 Elsevier Ltd. All rights reserved.

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