Objective: To thoroughly examine the mechanisms for insulin resistance in plycystic ovary syndrome (PCOS) and to evaluate the effects of pioglitazone treatment on insulin resistance, beta-cell function, LH secretion, and glucose metabolism. Design: Randomized, blinded, pacebo-controlled study. Setting: Outpatient clinic, at a university hospital in Denmark. Patient(s): Thirty obese women wity PCOS and 14 weight-matched healy females. Interventions: Sixteen weeks of blinded treatment with pioglitazone (30 mg/d) or placebo. Main Outcome Measure(s): Fasting blood samples, 24-hour 20-minute integrated blood sampling (LH, insulinm and C-peptide), euglycemic hyperinsulinemic clamps including 3-H-3 glucose and indirect calorimetry were operformed before and after the intervention period. Results: Patients with PCOS had significantly lower insulin sensitivity compared with controls, including significantly decreased insulin stimulate oxidative and nonoxidative glucose metabolism Pioglitazone treatment resulted in significantly lower levels of fasting Insulin and significantly higher insulin sensitivity increased insulin-stimulated glucose, oxidation and increased insulin-stimulated inhibition of lipid oxidation. During 24-hour blood sampling significantly under-the-curve insulin and lower, median insulin levels were observed Secretion profiies of LH and E-2 and T levels did not change significantly. Conclusion(s): Insulin resistance in PCOS was characterized by hyperinsulinemia impaired insulin stimulated oxidative and nonoxidative, glucose metabolism, 'which was partly reversed by pioglitazone treatment (Fertil Steril (R) 2006;86.385. (c) 2006 by American, Society for Reproductive Medicine)