| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Submitted on January 11, 2006
Accepted on June 9, 2006
All authors are associated with Oregon Health and Sciences University, Portland, Oregon 97239
* To whom correspondence should be addressed. E-mail: whelert{at}ohsu.edu.
Context: Several authors have reported the unsuspected finding of low cortisol levels (urinary, salivary and serum) in patients with PTSD.
Objective: To assess concentrations of cortisol and its predominant metabolites, cortisol production rate (CPR) and glucocorticoid receptor (GR) binding characteristics in PTSD compared with normal subjects.
Design: Matched PTSD patients and control subject had cortisol production rates determined by a stable isotope dilution technique after infusion of deuterated cortisol. Serum cortisol, urinary cortisol and its metabolites were measured by gas chromatography/mass spectroscopy (GS/MS). GR binding capacity (Ro) and ligand binding affinity (Kd) were measured in mononuclear leukocytes.
Setting: All subjects were tested during a 40 h admission in an inpatient Clinical Research Center.
Patients and Participants: Ten patients with PTSD were matched by age and gender with 10 controls.
Interventions: None.
Outcome Measures: Statistical comparison was conducted for various measures of cortisol in PTSD patients and normal subjects.
Results: No statistical difference was found in mean level or circadian pattern of cortisol secretion using serum or salivary immunoassay detection methods. Although in the normal range, urinary cortisol by immunoassay showed statistically lower values over a 24 h period in PTSD patients compared with controls. This finding was not confirmed by GC/MS determination of cortisol or its metabolites. CPR was not statistically different between these groups. GR also showed no alteration in (Ro) or (Kd) between the groups.
Conclusion: The data indicate that PTSD in the chronic and unprovoked state is not characterized by an acute "biological" stress response.
Read all eLetters
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |