SOMATOSTATIN TREATMENT REDUCES THE EXAGGERATED RESPONSE OF ADRENOCORTICOTROPIN HORMONE AND CORTISOL TO CORTICOTROPIN-RELEASING HORMONE IN POLYCYSTIC-OVARY-SYNDROME
A. Lanzone et al., SOMATOSTATIN TREATMENT REDUCES THE EXAGGERATED RESPONSE OF ADRENOCORTICOTROPIN HORMONE AND CORTISOL TO CORTICOTROPIN-RELEASING HORMONE IN POLYCYSTIC-OVARY-SYNDROME, Fertility and sterility, 67(1), 1997, pp. 34-39
Objective: To evaluate the influence of somatostatin analogue (octreot
ide) in the function of hypothalamic-pituitary-adrenal (HPA) axis in w
omen with polycystic ovary syndrome (PCOS). Setting: Women referred to
the Department of Obstetrics and Gynecology, Universita Cattolica del
Sacro Cuore. Patient(s): Twelve PCOS women and 12 normo-ovulatory con
trols. Intervention(s): In early follicular phase, I mu g/kg human cor
ticotrophin-releasing hormone (CRH) was injected at 9:00 A.M. and bloo
d samples were collected for 90 minutes after stimulus; ACTH and corti
sol plasma levels were measured. The following day at 8:00 A.M., PCOS
patients received an ACTH test (250 mu g IV) and samples were collecte
d 60 minutes after injection. After 6 weeks of octreotide treatment (1
00 mg SC twice daily), PCOS patients repeated the same study. Main Out
come Measure(s): Plasma cortisol and ACTH concentrations. Result(s): T
he ACTH and cortisol baseline levels were similar in PCOS and control
patients. The responses to human CRH of ACTH (incremental area = 437.8
6 +/- 188.7 versus 175.78 +/- 87.6 pmol/L; mean +/- SD) and cortisol (
incremental area = 17,293.6 +/- 4,320.3 versus 5,885 (912.1 nmol/L) we
re significantly greater in PCOS with respect to control subjects. Aft
er octreotide treatment, ACTH response significantly decreased and no
difference was observed with respect to controls (incremental area = 1
76.94 +/- 91.4). Cortisol responses were decreased hy treatment. Howev
er, they remained significantly higher than in controls. Treatment did
not modify adrenal response to IV ACTH. Conclusion(s): Data suggest t
hat, in the HPA axis, hyperfunction of PCOS somatostatin could be invo
lved partially.