Pre-treatment cortisol awakening response predicts symptom reduction in posttraumatic stress disorder after treatment

被引:20
|
作者
Rapcencu, A. E. [1 ,2 ]
Gorter, R. [1 ,5 ]
Kennis, M. [3 ,5 ]
van Rooij, S. J. H. [4 ]
Geuze, E. [1 ,5 ]
机构
[1] Minist Def, Res Ctr Mil Mental Healthcare, Utrecht, Netherlands
[2] Netherlands Inst Forens Psychiat & Psychol, Utrecht, Netherlands
[3] Univ Utrecht, Dept Clin Psychol, Utrecht, Netherlands
[4] Emory Univ, Sch Med, Dept Psychiat & Behav Sci, Atlanta, GA USA
[5] Univ Med Ctr Utrecht, Dept Psychiat, Brain Ctr Rudolf Magnus, Utrecht, Netherlands
关键词
Cortisol awakening response; Neuroendocrinology; PTSD; Treatment; Veterans; Trauma; HPA-axis; Gortisol; Biomarker; SALIVARY CORTISOL; TRIPARTITE MODEL; PTSD TREATMENT; DEPRESSION; REACTIVITY; VETERANS; ANXIETY; TRAUMA; AXIS; PSYCHOTHERAPY;
D O I
10.1016/j.psyneuen.2017.04.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dysfunction of the HPA-axis has frequently been found in the aftermath of trauma exposure with or without PTSD. Decreasing HPA-axis reactivity to different stress cues has been reported during PTSD treatment. The cortisol awakening response (CAR) is a well-validated, standardized measure of HPA-axis reactivity which can be easily acquired in the clinical setting. Whether CAR(i) changes over time in traumatized individuals are specific to PTSD treatment is unknown. Furthermore, a possible role for the baseline CAR(i) in predicting symptom reduction after treatment in PTSD has not been examined before. To answer these questions, a cohort study was conducted in which the awakening cortisol was measured in both PTSD (N = 41) and non-PTSD (N = 25) combat-exposed male subjects. Measurements took place at inclusion and 6-8 months after inclusion for both the PTSD and the non-PTSD group. During the 6-8 months interval, PTSD patients received trauma-focused focused psychotherapy, whereas non-PTSD patients received no treatment. We found a decrease in the CAR(i) over time in both groups, suggesting it was not specific to PTSD or the effect of treatment. Therefore, caution is warranted when attributing diminished HPA-axis reactivity over time to effects of PTSD treatment. Second, CAR(i) prior to treatment predicted PTSD symptom reduction (CAPS score change) after treatment, and accounted for 10% of the variance, even when adjusted for changes in depressive symptoms and medication use during the study period. A putative role emerges for CAR(i) as a predictive biomarker of symptom reduction in male individuals with combat-related PTSD.
引用
收藏
页码:1 / 8
页数:8
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