Basal circadian and pulsatile ACTH and cortisol secretion in patients with fibromyalgia and/or chronic fatigue syndrome

被引:166
作者
Crofford, LJ [1 ]
Young, EA
Engleberg, NC
Korszun, A
Brucksch, CB
McClure, LA
Brown, MB
Demitrack, MA
机构
[1] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Neuronetics, Malvern, PA USA
[3] Univ Michigan, Sch Publ Hlth, Dept Biostat, Ann Arbor, MI 48109 USA
[4] Cardiff Univ, Coll Med, Cardiff CF1 3NS, S Glam, Wales
[5] Univ Michigan, Sch Med, Dept Psychiat, Ann Arbor, MI USA
关键词
D O I
10.1016/j.bbi.2003.12.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
The objective of this study was to evaluate and compare the basal circadian and pulsatile architecture of the HPA axis in groups of patients with FMS, CFS, or both syndromes with individually matched control groups. Forty patients with either FMS (n = 13), FMS and CFS (n = 12), or CFS (n = 15) were matched by age (18-65), sex, and menstrual status to healthy controls. Subjects were excluded if they met criteria for major Axis I psychiatric disorders by structured clinical interview (SCID). Subjects were admitted to the General Clinical Research Center where meals and activities were standardized. Blood was collected from an intravenous line every 10 min over 24 h for analysis of ACTH and cortisol. Samples were evaluable for ACTH in 36 subject pairs and for cortisol in 37 subject pairs. There was a significant delay in the rate of decline from acrophase to nadir for cortisol levels in patients with FMS (P < .01). Elevation of cortisol in the late evening quiescent period was evident in half of the FMS patients compared with their control group, while cortisol levels were numerically, but not significantly, lower in the overnight period in patients with CFS compared with their control group. Pulsatility analyses did not reveal statistically significant differences between patient and control groups. We conclude that the pattern of differences for basal circadian architecture of HPA axis hormones differs between patients with FMS and CFS compared to their matched control groups. The abnormalities in FMS patients are consistent with loss of HPA axis resiliency. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:314 / 325
页数:12
相关论文
共 43 条
[1]
Reduced hypothalamic-pituitary and sympathoadrenal responses to hypoglycemia in women with fibromyalgia syndrome [J].
Adler, GK ;
Kinsley, BT ;
Hurwitz, S ;
Mossey, CJ ;
Goldenberg, DL .
AMERICAN JOURNAL OF MEDICINE, 1999, 106 (05) :534-543
[2]
Mineralocorticoid receptor blockade by canrenoate increases both spontaneous and stimulated adrenal function in humans [J].
Arvat, E ;
Maccagno, B ;
Giordano, R ;
Pellegrino, M ;
Broglio, F ;
Gianotti, L ;
Maccario, M ;
Camanni, F ;
Ghigo, E .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (07) :3176-3181
[3]
INFLUENCES OF CORTICOTROPIN-RELEASING HORMONE, ADRENOCORTICOTROPIN, AND CORTISOL ON SLEEP IN NORMAL MAN [J].
BORN, J ;
SPATHSCHWALBE, E ;
SCHWAKENHOFER, H ;
KERN, W ;
FEHM, HL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1989, 68 (05) :904-911
[4]
Fibromyalgia and chronic fatigue syndrome - Similarities and differences [J].
Buchwald, D .
RHEUMATIC DISEASE CLINICS OF NORTH AMERICA, 1996, 22 (02) :219-+
[5]
BUYSSE DJ, 1991, SLEEP, V14, P331
[6]
Catley D, 2000, ARTHRIT CARE RES, V13, P51, DOI 10.1002/1529-0131(200002)13:1<51::AID-ART8>3.0.CO
[7]
2-Q
[8]
THE CONCEPTS OF STRESS AND STRESS SYSTEM DISORDERS - OVERVIEW OF PHYSICAL AND BEHAVIORAL HOMEOSTASIS [J].
CHROUSOS, GP ;
GOLD, PW .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1992, 267 (09) :1244-1252
[9]
Chronic pain and fatigue syndromes: Overlapping clinical and neuroendocrine features and potential pathogenic mechanisms [J].
Clauw, DJ ;
Chrousos, GP .
NEUROIMMUNOMODULATION, 1997, 4 (03) :134-153
[10]
HYPOTHALAMIC-PITUITARY-ADRENAL AXIS PERTURBATIONS IN PATIENTS WITH FIBROMYALGIA [J].
CROFFORD, LJ ;
PILLEMER, SR ;
KALOGERAS, KT ;
CASH, JM ;
MICHELSON, D ;
KLING, MA ;
STERNBERG, EM ;
GOLD, PW ;
CHROUSOS, GP ;
WILDER, RL .
ARTHRITIS AND RHEUMATISM, 1994, 37 (11) :1583-1592