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Insulin resistance is believed to be an integral component of the polycystic ovary syndrome (PCOS). Beta ( ß ) cell dysfunction is also found in PCOS. In the study, we determined the influence of age, body mass index (BMI), and waist-to-hip ratio (WHR) on insulin response to oral glucose load (OGTT) and on insulin sensitivity (Si) and ß -cell function in young women with PCOS. One hundred fourteen patients with PCOS and 41 controls with normal basal plasma glucose were studied. A 75-g OGTT was performed to determine glucose tolerance and insulin response. Insulin sensitivity and ß -cell function were studied using a modified frequently sampled IV glucose tolerance test (FISGTT) to determine the acute insulin response (AIR G ), as well as S i by minimal model analysis. S i was decreased in PCOS women (2.49 0.18 vs. 3.41 ± 0.36, p < 0.05), but no difference in AIR G existed between the PCOS and control group (75.1 ± 4.6 vs. 63.4 ± 4.6, p < 0.05). BMI and WHR correlated negatively with S i ( r  = -0.43; r  = -0.289, p < 0.001, respectively), but not with AIR G ( r  = 0.116; r  = -0.02, p > 0.05, respectively). Increasing age correlated negatively with AIR G ( r  = -0.285, p < 0.001). There was a significant interaction between disease (PCOS), BMI, and WHR on S i as well as between age and PCOS on AIR G . Thus, patients below the age of 25 with PCOS showed enhanced AIR G (89.5 ± 7.1 vs. 65.1 ± 6.7, p < 0.05) and decreased S i (2.43 ± 0.25 vs. 4.52 ± 0.62, p < 0.05) compared to age-matched controls. In conclusion, these data suggest that not all patients with PCOS have basal and stimulated hyperinsulinemia, insulin resistance, and impaired glucose tolerance. Based on these data in young PCOS subjects, the development of insulin resistance and T2DM may be prevented with appropriate treatment strategies., Competing Interests: The authors declare that there are no conflicts of interest regarding the publication of this paper., (Copyright © 2022 Mirjana Šumarac-Dumanović et al.)