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Keywords :
Adult; C-Peptide/analysis; Contraceptives, Oral, Combined/pharmacology; Cyproterone Acetate/pharmacology; Drug Combinations; Ethinyl Estradiol/pharmacology; Female; Glucose/metabolism; Glucose Tolerance Test; Humans; Insulin/metabolism/pharmacology; Metabolic Clearance Rate; OT - Biology; OT - Carbohydrate Metabolic Effects; OT - Contraception; OT - Contraceptive Methods; OT - Family Planning; OT - *Glucose Metabolism Effects; OT - *Metabolic Effects; OT - Oral Contraceptives; OT - *Oral Contraceptives, Combined; OT - *Oral Contraceptives, Low-dose; OT - Physiology; OT - *Prospective Studies; OT - Research Methodology; OT - *Research Report; OT - Studies
Abstract :
[en] OBJECTIVE: To study the effects of the slightly estrogen-dominant monophasic low-dose oral contraceptive (OC) Diane-35 (Schering AG, Berlin, Germany) (35 micrograms ethinyl estradiol [EE2] + 2 mg cyproterone acetate, a 17 alpha-hydroxyprogesterone derivative [17-OHP]) on glucose and insulin metabolism. DESIGN: Seven healthy young women were investigated by using the euglycemic hyperinsulinemic glucose clamp technique (insulin delivery rate = 100 mU/kg per hour for 120 minutes). This test was performed, after an overnight fast, during the last 7 days of a spontaneous cycle and within the last 5 days of pill intake during the sixth and twelfth cycle of a continuous treatment with Diane-35 in each subject. RESULTS: The three indexes measuring the insulin-induced glucose disposal during the clamp (glucose infusion rate, glucose metabolic clearance rate, and glucose infusion rate divided by plasma insulin plateau levels) were not significantly affected by Diane-35. In contrast, the metabolic clearance rate of the exogenous insulin infused during the clamp tended to be slightly increased with Diane-35 (significant after 6 but not after 12 cycles). CONCLUSION: These results suggest that a 1-year treatment with the OC Diane-35, which contains EE2 + a 17-OHP rather than a 19-nortestosterone derivative as the progestogen compound, does not significantly alter peripheral (presumably muscular) insulin sensitivity but slightly increases insulin (presumably hepatic) clearance.
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