ORAL-CONTRACEPTIVE THERAPY FOR POLYCYSTIC OVARY DISEASE AFTER CHRONICGONADOTROPIN-RELEASING AGONIST ADMINISTRATION - PREDICTORS OF CONTINUED OVARIAN SUPPRESSION
Ke. Elkindhirsch et al., ORAL-CONTRACEPTIVE THERAPY FOR POLYCYSTIC OVARY DISEASE AFTER CHRONICGONADOTROPIN-RELEASING AGONIST ADMINISTRATION - PREDICTORS OF CONTINUED OVARIAN SUPPRESSION, Journal of reproductive medicine, 41(9), 1996, pp. 645-652
OBJECTIVE: To study the beneficial effects of oral contraceptive (OC)
therapy following gonadotropin-releasing hormone agonist (GnRH-a) admi
nistration in women with polycystic ovary disease (PCOD). STUDY DESIGN
: Twenty-three hyperandrogenic women (aged 15-39) were randomized into
two groups; GnRH-a (depot every 28 days) for six months or combinatio
n therapy (GnRH-a plus OC ''addback'') for six months. Following six m
onths of treatment with either therapy, all patients received OC thera
py for at least six months. The hormonal state wits evaluated at three
-month intervals. RESULTS: Hormone levels of luteinizing hormone (LH),
testosterone (T) and free T remained suppressed within the normal ran
ge in II of 17 patients (65%) during the six months of OC-only therapy
, while the other six patients showed ''escape'' from suppression, wit
h the LH, T and free T concentrations rising to pre-GnRH-a treatment l
evels. Use of Oc addback therapy did Mot potentiate the long-acting th
erapeutic effect of GnRH-a pretreatment; three of six patients in the
escape group were pretreated with combination therapy and three with G
nRH-a only. CONCLUSION: In the majority of women with PCOD, OC therapy
following GhRH-a administration was effective in maintaining ovarian
androgen Suppression. Failure to maintain ovarian suppression in this
patient population was associated with higher elevations of baseline f
ree T concentrations.