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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.
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页码:1 / 8
页数:8
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