Basal and dexamethasone suppressed salivary cortisol concentrations in a community sample of patients with posttraumatic stress disorder

被引:75
作者
Lindley, SE [1 ]
Carlson, EB [1 ]
Benoit, M [1 ]
机构
[1] Palo Alto Vet Affairs Hlth Care Syst, Dept Vet Affairs, Natl Ctr Posttraumat Stress Disorder, Menlo Pk, CA USA
关键词
dexamethasone; HPA axis; posttraumatic stress disorder; salivary cortisol; stress; trauma;
D O I
10.1016/j.biopsych.2003.12.021
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background. Posttraumatic stress disorder (PTSD) has been associated with lower concentrations of cortisol and enhanced suppression of cortisol by dexamethasone, although discrepancies exist among reports. The objective of the study was to determine the pattern of cortisol responses inpatients seeking treatment for PTSD resulting from a variety of traumatic experiences and to test whether cortisol responses are significantly related to childhood trauma, severity of symptoms, or length of time since trauma. Methods. Salivary cortisol was measured at 8 AM, 4 PM, and 10 PM on 2 consecutive days before and after a 10 PM dose of .5 mg dexamethasone in 17 psychotropic medication and substance-free subjects with PTSD and 17 matched control subjects. Results. Repeated-measures analysis of variance (ANOVA) of the baseline salivary cortisol concentrations demonstrated a significant effect for group with higher concentrations in the PTSD group but no significant differences in responses to dexamethasone. The presence of childhood abuse did not significantly affect salivary cortisol concentrations, and there was no correlation between predexamethasone cortisol and either the severity of PTSD symptoms or the time since the index trauma. Conclusions. Neither low basal concentrations nor enhanced suppression of cortisol are consistent markers of a PTSD diagnosis.
引用
收藏
页码:940 / 945
页数:6
相关论文
共 56 条
[1]   Stress hormone dysregulation at rest and after serotonergic stimulation among alcohol-dependent men with extended abstinence and controls [J].
Anthenelli, RM ;
Maxwell, RA ;
Geracioti, TD ;
Hauger, R .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2001, 25 (05) :692-703
[2]   Neopterin levels and dexamethasone suppression test in posttraumatic stress disorder [J].
Atmaca, M ;
Kuloglu, M ;
Tezcan, E ;
Onal, S ;
Ustundag, B .
EUROPEAN ARCHIVES OF PSYCHIATRY AND CLINICAL NEUROSCIENCE, 2002, 252 (04) :161-165
[3]  
Baker DG, 1999, AM J PSYCHIAT, V156, P585
[4]  
Barden N, 1999, J PSYCHIATR NEUROSCI, V24, P25
[5]  
Carlson E.B., 2000, Trauma, Violence, Abuse, V1, P4, DOI [DOI 10.1177/1524838000001001002, 10.1177/1524838000001001002]
[6]   Diurnal salivary cortisol in pediatric posttraumatic stress disorder [J].
Carrion, VG ;
Weems, CF ;
Ray, RD ;
Glaser, B ;
Hessl, D ;
Reiss, AL .
BIOLOGICAL PSYCHIATRY, 2002, 51 (07) :575-582
[7]   Adrenal insufficiency in critically ill emergency department patients: A Taiwan preliminary study [J].
Chang, SS ;
Liaw, SJ ;
Bullard, MJ ;
Chiu, TF ;
Chen, JC ;
Liao, HC .
ACADEMIC EMERGENCY MEDICINE, 2001, 8 (07) :761-764
[8]   Increased beclomethasone-induced vasoconstriction in women with posttraumatic stress disorder [J].
Coupland, NJ ;
Hegadoren, KM ;
Myrholm, J .
JOURNAL OF PSYCHIATRIC RESEARCH, 2003, 37 (03) :221-228
[9]   STRESS UPDATE - ADAPTATION OF THE HYPOTHALAMIC PITUITARY-ADRENAL AXIS TO CHRONIC STRESS [J].
DALLMAN, MF .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 1993, 4 (02) :62-69
[10]   Developmental traumatology Part I: Biological stress systems [J].
De Bellis, MD ;
Baum, AS ;
Birmaher, B ;
Keshavan, MS ;
Eccard, CH ;
Boring, AM ;
Jenkins, FJ ;
Ryan, ND .
BIOLOGICAL PSYCHIATRY, 1999, 45 (10) :1259-1270