Effects of Rosiglitazone in Obese Women with Polycystic Ovary Syndrome and Severe Insulin Resistance
Vicken Sepilian and
Manubai Nagamani
Department of Obstetrics and Gynecology, Division of Reproductive Endocrinology and Infertility, University of Texas Medical Branch, Galveston, Texas 77555
Address all correspondence and requests for reprints to: Manubai Nagamani, M.D., Department of Obstetrics & Gynecology, University of Texas Medical Branch, Galveston, Texas 77555-0587. E-mail: mnagaman{at}utmb.edu.
Our objective was to evaluate the effectiveness of the insulin-sensitizingagent rosiglitazone in obese women with polycystic ovary syndrome(PCOS) and severe insulin resistance. Twelve obese women withPCOS were recruited. All were hirsute and anovulatory with acanthosisnigricans indicating severe insulin resistance. All women weretreated with 4 mg of rosiglitazone daily for 6 months. A standard75-g oral glucose tolerance test with insulin levels was performedbefore and after the women were treated with rosiglitazone.Glucose and insulin areas under the curve (AUC) were calculated.Serum levels of total and free testosterone, dehydroepiandrosteronesulfate, LH, and 17-hydroxyprogesterone were also measured beforeand after treatment. The body mass index was determined beforeand after treatment. There was a highly significant (r = 0.881,P < 0.0001) positive correlation between insulin responseduring oral glucose tolerance test and basal total testosteronelevels. After treatment with rosiglitazone, there were significantdecreases in fasting insulin levels (46.0 ± 6.5 vs. 16.9± 2.0 µU/ml; P < 0.001), insulin AUC (749.3± 136.3 vs. 225.0 ± 15.7 µU/ml; P = 0.003),fasting glucose levels (90.8 ± 3.0 vs. 81.8 ±1.9 mg/dl; P = 0.003), and glucose AUC (437.9 ± 25.0vs. 322.5 ± 14.7 mg/dl; P < 0.001). Both total testosterone(96.3 ± 17.3 vs. 56.1 ± 5.8 ng/dl; P = 0.01) andfree testosterone (5.8 ± 0.6 vs. 3.4 ± 0.5 pg/ml;P < 0.001) decreased significantly after treatment, althoughthere was no significant change in LH levels. Levels of SHBGincreased significantly (18.3 ± 3.4 vs. 25.8 ±6.6 nmol/liter; P = 0.009) after treatment, and dehydroepiandrosteronesulfate levels decreased significantly (P = 0.04). There wasno significant change in body mass index (40.4 ± 2.4vs. 41.1 ± 2.7 kg/m2). Eleven of the women reverted toregular ovulatory cycles during the treatment period. We concludethat 1) rosiglitazone therapy improves insulin resistance andglucose tolerance in obese women with PCOS; 2) rosiglitazonedecreases ovarian androgen production, which appears to be independentof any changes in LH levels; 3) hyperinsulinemia appears toplay a key role in the overproduction of ovarian androgens inthese women because attenuation of insulin levels is associatedwith decreased testosterone levels; and 4) short-term rosiglitazonetherapy helps restore spontaneous ovulation.
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