A randomized controlled study comparing the endocrine effects of pulsatileintravenous gonadotropin-releasing hormone after gonadotropin-releasing hormone agonist pretreatment versus clomiphene citrate in patients with polycystic ovary syndrome
Ecm. Timmerman-van Kessel et al., A randomized controlled study comparing the endocrine effects of pulsatileintravenous gonadotropin-releasing hormone after gonadotropin-releasing hormone agonist pretreatment versus clomiphene citrate in patients with polycystic ovary syndrome, FERT STERIL, 73(6), 2000, pp. 1145-1148
Objective: To compare the endocrine changes in the follicular phase in infe
rtile patients with polycystic ovary syndrome (PCOS) treated with either pu
lsatile IV GnRH after GnRH-agonist (GnRH-a) downregulation or clomiphene ci
trate (CC).
Design: Subgroup analysis within a randomized, controlled, multicenter stud
y.
Setting: Women referred to the Infertility Clinic, Catharina Hospital Eindh
oven, The Netherlands.
Patient(s): Twenty-eight infertile patients with PCOS. Intervention(s): Pat
ients were randomly assigned to pulsatile IV GnRH (10-20 mu g/90 min) after
GnRH-a down-regulation or CC (50-150 mg; cycle days 3-7). Patients were mo
nitored on alternate days with ovarian sonography and serum concentrations
of E-2, LH, and FSH. Serum P and songraphy confirmed ovulation.
Main Outcome Measure(s): Serum concentrations of E-2, LH, and FSH were asse
ssed before treatment was started and after each ovarian sonography.
Result(s): In ovulatory cycles, no statistically significant differences we
re observed during the follicular phase comparing serum concentrations of E
-2, LH, and FSH between the treatments. However, a significant increase in
LH occurred in the GnRH group.
Conclusion(s): No significant endocrine differences were observed between G
nRH and CC treatment. However, there was a significant increase in the seru
m LH concentration during the follicular phase in the GnRH group. Increment
s of LH in the GnRH group may be due to recovery of endogenous LH secretion
. (C) 2000 by American Society for Reproductive Medicine.