H. Medenvrtovec, GNRH ANALOG ADMINISTRATION IN PATIENTS WITH POLYCYSTIC OVARIAN DISEASE, International journal of gynaecology and obstetrics, 50(2), 1995, pp. 179-183
Objective: To evaluate the hormonal response to the short protocol of
gonadotropin-releasing hormone (GnRH) analog (GnRHa) in patients with
polycystic ovarian disease (PCOD). Methods: We enrolled 35 patients (2
0 infertile) with ultrasonographic and hormonal PCOD characteristics.
GnRHa Suprefact was applied subcutaneously at a daily dose of 0.9 ml f
or 9 consecutive days starting on the 10th-15th day after induced or s
pontaneous bleeding. Blood sampling for follicle-stimulating hormone (
FSH), luteinizing hormone (LH), testosterone (T), estradiol (E(2)), es
trone (E(1)) and dehydroepiandrosterone sulfate (DHEA-S) was performed
before the treatment and on days 3 and 4 of GnRHa administration. Stu
dent's t-test was used for the analysis of differences between various
mean values. All statistical analyses were performed by the computeri
zed statistical package CSS-Statistica. Results: Pretreatment hormonal
levels (FSH 5.68 +/- 1.86 IU/I, LH 14.16 +/- 1.72 IU/I, E(2) 0.29 +/-
0.20 nmol/l, E(1) 0.35 +/- 0.17 nmol/l, T 3.52 +/- 1.40 nmol/l, DHEA-
S 7.15 +/- 2.89 mu mol/l) barely differed on day 3 of GnRHa administra
tion, except for the rise in LH (17.14 +/- 10.97 IU/I), which was stil
l not significant. On day 9 of GnRHa application, significant suppress
ion of FSH (3.16 +/- 1.55 IU/1) and LH (8.05 +/- 5.00 IU/I) was regist
ered compared with pretreatment levels, without changes in the FSH:LH
ratio, and in other parameters studied. Although there were no changes
in ultrasound characteristics on day 9 of GnRHa administration compar
ed with basal findings, bleeding occurred 14-18 days after the last Gn
RHa dose in 32 patients. There were three pregnancies out of 20 infert
ile patients in the treated cycles. Conclusion: Significant suppressio
n of FSH and LH in PCOD patients does not interfere with ovarian stero
id production, which is probably maintained due to higher follicular s
ensitivity to normal FSH and LH levels. Alternatively it may be the co
nsequence of the unaltered FSH:LH ratio in spite of GnRHa-suppressed a
bsolute values. However the recommencement of menstrual bleeding and 1
5% of pregnancies in the investigated infertile patients suggest the o
ccurrence of certain temporary intraovarian events, which probably con
tinue after the cessation of GnRHa administration.