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Volume 61, Issue 8, Pages 952-956 (15 April 2007)


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Effects of Metyrapone on Hypothalamic-Pituitary-Adrenal Axis and Sleep in Women with Post-Traumatic Stress Disorder

Christian Otteabd, Maryann Lenocib, Thomas Metzlerb, Rachel Yehudac, Charles R. Marmarab, Thomas C. NeylanabCorresponding Author Informationemail address

Received 24 October 2005; received in revised form 16 March 2006 and 2 August 2006; accepted 7 August 2006. published online 09 March 2007.

Background

Metyrapone blocks cortisol synthesis which results in removal of negative feedback, a stimulation of hypothalamic corticotropin releasing factor (CRF) and a reduction in delta sleep. We previously reported a diminished delta sleep and hypothalamic-pituitary-adrenal (HPA) response to metyrapone in men with post-traumatic stress disorder (PTSD). In this study, we aimed to extend these findings to women.

Methods

Three nights of polysomnography were obtained in 17 women with PTSD and 16 controls. On day 3, metyrapone was administered throughout the day up until bedtime. Plasma adrenocorticotropic hormone (ACTH), cortisol, and 11-deoxycortisol were obtained the morning following sleep recordings the day before and after metyrapone administration.

Results

There were no significant between-group differences in hormone concentration and delta sleep at baseline. Relative to controls, women with PTSD had decreased ACTH and delta sleep responses to metyrapone. Decline in delta sleep was associated with the magnitude of increase in ACTH across groups.

Conclusions

Similar to our previous findings in men, the ACTH and sleep electroencephalogram response to metyrapone is attenuated in women with PTSD. These results are consistent with a model of downregulation of CRF receptors in an environment of chronically increased CRF activity or with enhanced negative feedback regulation in PTSD.

a Department of Psychiatry, University of California, San Francisco, California

b Veterans Affairs Medical Center, San Francisco, California

c Department of Psychiatry, Mount Sinai School of Medicine, New York, New York

d Department of Psychiatry, University Hospital Hamburg-Eppendorf, Hamburg, Germany.

Corresponding Author InformationAddress reprint requests to Thomas C. Neylan, M.D., Veterans Affairs Medical Center, 4150 Clement Street (116 P), San Francisco, CA 94121

PII: S0006-3223(06)01067-5

doi:10.1016/j.biopsych.2006.08.018


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