Hypothalamic-pituitary-adrenal axis function in patients with chronic depression

被引:98
作者
Watson, S [1 ]
Gallagher, P [1 ]
Del-Estal, D [1 ]
Hearn, A [1 ]
Ferrier, IN [1 ]
Young, AH [1 ]
机构
[1] Univ Newcastle, Stanley Fdn Res Ctr, Sch Neurosci & Psychiat, Royal Victoria Infirm, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
关键词
D O I
10.1017/S0033291702005998
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background. Hypothalamic-pituitary-adrenal (HPA) axis function in patients with chronic depression has previously been shown to be normal when measured using the dexamethasone suppression test (DST). We examined patients with chronic depression using the sensitive dexamethasone/corticotropin releasing hormone (dex/CRH) test and the dexamethasone suppression test (DST) to establish whether HPA axis abnormalities are present in this group. We also compared the sensitivity of the two tests and compared the results with previous studies in depression that have not specifically selected chronic patients. Method. Twenty-nine patients with the chronic subtype of major depressive disorder and 28 matched controls underwent examination of HPA axis function. Results. Neither the cortisol response to the DST or the dex/CRH test differed significantly between the patient and control groups. There was a trend in favour of more patients than controls having an abnormal response to the dex/CRH test (P = 0(.)052). Neither the patients with an abnormally enhanced response, nor the magnitude of response could be predicted by any illness or demographic variable. Conclusion. The HPA axis is not overtly abnormal in chronic depression. This contrasts with previous findings in acute depression and bipolar disorder and may suggest that the HPA axis abnormalities present in acute depression resolve, but are not accompanied by symptom resolution. Alternatively, a subgroup of depressives with less HPA dysfunction may progress to chronicity. This has implications for treatment and prognosis. The dex/CRH is a more sensitive test of HPA axis function than the DST in patients with chronic depression.
引用
收藏
页码:1021 / 1028
页数:8
相关论文
共 31 条
[1]  
Altman D., 2000, STAT CONFIDENCE
[2]   Cognitive-behavioral management of drug-resistant major depressive disorder [J].
Fava, GA ;
Savron, G ;
Grandi, S ;
Rafanelli, C .
JOURNAL OF CLINICAL PSYCHIATRY, 1997, 58 (06) :278-282
[3]  
First M.B., 2007, STRUCTURED CLIN INTE
[4]  
GALLAGHER P, 2001, J PSYCHOPHARMACOL S3, V15, pA15
[5]   Risk for bipolar illness in patients initially hospitalized for unipolar depression [J].
Goldberg, JF ;
Harrow, M ;
Whiteside, JE .
AMERICAN JOURNAL OF PSYCHIATRY, 2001, 158 (08) :1265-1270
[6]  
HAYS RD, 1995, ARCH GEN PSYCHIAT, V52, P11
[7]   Fortnighly review - Stress, the brain, and mental illness [J].
Herbert, J .
BRITISH MEDICAL JOURNAL, 1997, 315 (7107) :530-535
[8]   THE COMBINED DEXAMETHASONE CRH TEST - A REFINED LABORATORY TEST FOR PSYCHIATRIC-DISORDERS [J].
HEUSER, I ;
YASSOURIDIS, A ;
HOLSBOER, F .
JOURNAL OF PSYCHIATRIC RESEARCH, 1994, 28 (04) :341-356
[9]  
Heuser IJE, 1996, AM J PSYCHIAT, V153, P93
[10]   Psychosocial disability during the long-term course of unipolar major depressive disorder [J].
Judd, LL ;
Akiskal, HS ;
Zeller, PJ ;
Paulus, M ;
Leon, AC ;
Maser, JD ;
Endicott, J ;
Coryell, W ;
Kunovac, JL ;
Mueller, TI ;
Ricc, JP ;
Keller, MB .
ARCHIVES OF GENERAL PSYCHIATRY, 2000, 57 (04) :375-380