Neuroendocrine biomarkers of prolonged exposure treatment response in military-related PTSD
- PMID: 32554173
- DOI: 10.1016/j.psyneuen.2020.104749
Neuroendocrine biomarkers of prolonged exposure treatment response in military-related PTSD
Erratum in
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Corrigendum to "Neuroendocrine biomarkers of prolonged exposure treatment response in military-related PTSD" [Psychoneuroendocrinology (2020) Article 104749].Psychoneuroendocrinology. 2020 Oct;120:104802. doi: 10.1016/j.psyneuen.2020.104802. Epub 2020 Jul 10. Psychoneuroendocrinology. 2020. PMID: 32732021 No abstract available.
Abstract
Posttraumatic stress disorder (PTSD) is associated with dysregulation of the neuroendocrine system, including cortisol, allopregnanolone, and pregnanolone. Preliminary evidence from animal models suggests that baseline levels of these biomarkers may predict response to PTSD treatment. We report the change in biomarkers over the course of PTSD treatment. Biomarkers were sampled from individuals participating in (1) a randomized controlled trial comparing a web-version of Prolonged Exposure (Web-PE) therapy to in-person Present-Centered Therapy (PCT) and (2) from individuals participating in a nonrandomized effectiveness study testing PE delivered in-person as part of an intensive outpatient PTSD program. We found that higher cortisol reactivity during script-driven imagery was associated with higher baseline PTSD severity and that baseline allopregnanolone, pregnanolone, and cortisol reactivity were associated with PTSD treatment responder status over the course of intensive outpatient treatment. These findings demonstrate that peripherally assessed biomarkers are associated with PTSD severity and likelihood of successful treatment outcome of PE delivered daily over two weeks. These assessments could be used to determine which patients are likely to respond to treatment and which patients require augmentation to increase the likelihood of optimal response to PTSD treatment.
Keywords: Allopregnanolone; Cortisol; DHEA; Posttraumatic stress disorder; Pregnanolone; Treatment.
Published by Elsevier Ltd.
Conflict of interest statement
Declaration of Competing Interest Dr. Rauch receives support from Wounded Warrior Project (WWP), Department of Veterans Affairs (VA), National Institute of Health (NIH), Woodruff Foundation, and Department of Defense (DOD). Dr. Rauch receives royalties from Oxford University Press. Dr. Sripada is supported by U.S. Department of Veterans Affairs Health Services Research & Development Service. Mark Burton has nothing to disclose. Dr. Michopoulos receives support from the National Institute of Health (NIH). Kimberly Kerley has nothing to disclose. Christine E. Marx has nothing to disclose. Jason D. Kilts has nothing to disclose. Dr. Naylor receives support from the Department of Veterans Affairs (VA). Dr. Rothbaum receives support from the Wounded Warrior Project, Department of Defense, National Institute of Mental Health, and McCormick Foundation. Dr. Rothbaum receives royalties from Oxford University Press, Guilford, APPI, and Emory University and received one advisory board payment from Genentech, Jazz Pharmaceuticals, and Aptinyx. Carmen P. McLean has nothing to disclose. Dr. Smith receives support from NIH. Dr. Norrholm receives support from the Department of Veterans Affairs (VA) and Department of Defense (DOD). Dr. Jovanovic receives funding from NIH and Brain and Behavior Research Foundation Dr. Liberzon receives support from National Institute of Health (NIH), Cohen Veterans Bioscience, and Department of Defense (DOD). Douglas E. Williamson has nothing to disclose. COL Jeffrey S. Yarvis has nothing to disclose. Katherine A. Dondanville has nothing to disclose. Dr. Young-McCaughan receives support as part of her work supporting research studies from the Department of Defense (DOD), Department of Veterans Affairs (VA), and the National Institutes of Health (NIH). Terence M. Keane has nothing to disclose. Alan L. Peterson has nothing to disclose.
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