Enhanced corticotropin response to corticotropin-releasing hormone as a predictor of mania in euthymic bipolar patients

1999 ◽  
Vol 29 (4) ◽  
pp. 971-978 ◽  
Author(s):  
E. VIETA ◽  
M. J. MARTÍNEZ-DE-OSABA ◽  
F. COLOM ◽  
A. MARTÍNEZ-ARÁN ◽  
A. BENABARRE ◽  
...  

Background. Dysregulation of corticotropin (ACTH) and cortisol response after corticotropin-releasing hormone (CRH) stimulation has been reported in bipolar patients. Most findings involve the pathophysiology of the depressive phase of the illness and its prediction. However, the possible predictive value of the CRH challenge test with respect to manic episodes remains unknown.Methods. The ACTH and free cortisol response to the injection of 100 μg of synthetic human CRH and plasma cortisol-binding globulin levels were measured in 42 lithium-treated patients suffering from Research Diagnostic Criteria bipolar I disorder in remission, and 21 age- and sex-matched normal controls. A 1-year follow-up was conducted to assess any possible relationship between outcome and the hormonal response.Results. Bipolar patients showed higher baseline and peak ACTH concentrations than control subjects. A higher area under ACTH concentration curve after CRH stimulation predicted manic/hypomanic relapse within 6 months by multiple regression analysis.Conclusion. Bipolar patients in remission show mild abnormalities in ACTH levels before and after CRH stimulation. CRH challenge may be a potentially good predictor of manic or hypomanic relapse in remitted bipolar patients.

1995 ◽  
Vol 38 (12) ◽  
pp. 803-807 ◽  
Author(s):  
Claas-H. Lammers ◽  
Diego Garcia-Borreguero ◽  
Jürgen Schmider ◽  
Ulrike Gotthardt ◽  
Michael Dettling ◽  
...  

1997 ◽  
Vol 20 (8) ◽  
pp. 476-481 ◽  
Author(s):  
Hazra S. Moeniralam ◽  
E. Endert ◽  
J. J. B. van Lanschot ◽  
H. P. Sauerwein ◽  
J. A. Romijn

1989 ◽  
Vol 120 (3) ◽  
pp. 390-394 ◽  
Author(s):  
Katsumi Goji

Abstract. The human corticotropin-releasing hormone (hCRH) tests were performed in twelve normal short children, and the responses of plasma ACTH and cortisol to iv administration of 1 μg/kg hCRH were compared with those to insulin-induced hypoglycemia. After administration of hCRH, the mean plasma ACTH level rose from a basal value of 3.3 ± 0.4 pmol/l (mean ± sem) to a peak value of 9.2 ± 0.8 pmol/l at 30 min, and the mean plasma cortisol level rose from a basal value of 231 ± 25 nmol/l to a peak value of 546 ± 30 nmol/l at 30 min. The ACTH response after insulin-induced hypoglycemia was greater than that after hCRH administration; the mean peak level (P < 0.01), the percent maximum increment (P < 0.01), and the area under the ACTH response curve (P < 0.01) were all significantly greater after insulin-induced hypoglycemia than those after hCRH administration. Although the mean peak cortisol level after insulin-induced hypoglycemia was about 1.3-fold higher than that after hCRH administration (P < 0.01), neither the percent maximum increment in plasma cortisol nor the area under the cortisol response curve after insulin-induced hypoglycemia was significantly different from that after hCRH administration. Consequently, the acute increases in plasma ACTH after the administration of 1 μg/kg hCRH stimulated the adrenal gland to almost the same cortisol response as that obtained with a much greater increase in plasma ACTH after insulin-induced hypoglycemia. These results suggest that a plasma ACTH peak of 9–11 pmol/l produces near maximum acute stimulation of adrenal steroidgenesis.


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