Enhanced cortisol suppression in response to dexamethasone administration in traumatized veterans with and without posttraumatic stress disorder

被引:124
作者
de Kloet, C. S.
Vermetten, E.
Heijnen, C. J.
Geuze, E.
Lentjes, E. G. W. M.
Westenberg, H. G. M.
机构
[1] Cent Mil Hosp, Dept Mil Psychiat, NL-3584 CX Utrecht, Netherlands
[2] Univ Utrecht, Med Ctr, Rudolf Magnus Inst Neurosci, Dept Psychiat, Utrecht, Netherlands
[3] Univ Utrecht, Med Ctr, Lab Psychoneuroimmunol, Utrecht, Netherlands
[4] Univ Utrecht, Med Ctr, Dept Clin Chem & Haematol, Lab Endocrinol, Utrecht, Netherlands
关键词
PTSD; dexamethasone suppression test; cortisol; HPA-axis; corticosteroid binding globulin; saliva;
D O I
10.1016/j.psyneuen.2006.12.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: While enhanced cortisol suppression in response to dexamethasone is one of the most consistent biological findings in posttraumatic stress disorder (PTSD), the relative contribution of trauma exposure to this finding remains unclear. Methods: Assessment of diurnal salivary cortisol levels and 1600h salivary cortisol before and after oral administration of 0.5 mg dexamethasone in veterans with PTSD, veterans without PTSD (trauma controls) and healthy controls. Assessment of 1600h plasma cortisol, ACTH and corticotrophin binding globulin (CBG) in response to dexamethasone in PTSD patients and trauma controls. Results: Both PTSD patients and trauma controls demonstrated significantly more salivary cortisol suppression compared to healthy controls. Salivary cortisol, plasma cortisol and ACTH suppression as well as CBG levels did not differ between PTSD patients and trauma controls. PTSD patients showed a reduced awakening cortisol response (ACR) compared to healthy controls that correlated significantly with PTSD symptoms. No significant differences were observed in ACR between PTSD patients and trauma controls. Conclusions: These data suggest that enhanced cortisol suppression to dexamethasone is related to trauma exposure and not specifically to PTSD. The correlation between the ACR and PTSD severity suggests that a flattened ACR may be a result of clinical symptoms. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:215 / 226
页数:12
相关论文
共 61 条
[1]  
[Anonymous], 1994, AM PSYCHIATR ASSOC
[2]   Glucocorticoid receptor polymorphisms and post-traumatic stress disorder [J].
Bachmann, AW ;
Sedgley, TL ;
Jackson, RV ;
Gibson, JN ;
Young, RMD ;
Torpy, DJ .
PSYCHONEUROENDOCRINOLOGY, 2005, 30 (03) :297-306
[3]  
Baker DG, 1999, AM J PSYCHIAT, V156, P585
[4]   Higher levels of basal serial CSF cortisol in combat veterans with posttraumatic stress disorder [J].
Baker, DG ;
Ekhator, NN ;
Kasckow, JW ;
Dashevsky, B ;
Horn, PS ;
Bednarik, L ;
Geracioti, TD .
AMERICAN JOURNAL OF PSYCHIATRY, 2005, 162 (05) :992-994
[5]   Behavioral and physiological characterization of mate mice under chronic psychosocial stress [J].
Bartolomucci, A ;
Pederzani, T ;
Sacerdote, P ;
Panerai, AE ;
Parmigiani, S ;
Palanza, P .
PSYCHONEUROENDOCRINOLOGY, 2004, 29 (07) :899-910
[6]   Increased salivary cortisol after waking in depression [J].
Bhagwagar, Z ;
Hafizi, S ;
Cowen, PJ .
PSYCHOPHARMACOLOGY, 2005, 182 (01) :54-57
[7]  
BLAKE DD, 1995, J TRAUMA STRESS, V8, P75, DOI 10.1002/jts.2490080106
[8]   Diseases among men 20 years after exposure to severe stress: Implications for clinical research and medical care [J].
Boscarino, JA .
PSYCHOSOMATIC MEDICINE, 1997, 59 (06) :605-614
[9]   Posttraumatic stress disorder and physical illness - Results from clinical and epidemiologic studies [J].
Boscarino, JA .
BIOBEHAVIORAL STRESS RESPONSE: PROTECTIVE AND DAMAGING EFFECTS, 2004, 1032 :141-153
[10]  
Bremner JD, 1997, AM J PSYCHIAT, V154, P624