4.6 Article

Urinary Metabolites Reveal Hyperinsulinemia and Insulin Resistance in Polycystic Ovarian Syndrome (PCOS)

Journal

METABOLITES
Volume 11, Issue 7, Pages -

Publisher

MDPI
DOI: 10.3390/metabo11070437

Keywords

PCOS; insulin resistance; hyperinsulinemia; urine metabolomics

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This study identified a noninvasive method to properly evaluate insulin metabolism in young non-diabetic PCOS patients, showing promise in providing a more accurate and early diagnosis. Metabolomics could potentially lead to identification of biomarkers for exaggerated insulin response in OGTT, leading to substantial progress in PCOS diagnosis.
The identification of insulin resistance and hyperinsulinemia in polycystic ovary syndrome (PCOS) is not a minor issue. The homeostasis model assessment of insulin resistance index (HOMA) is the most used index of IR (Insulin Resistance), validated in overweight and obese patients but not in normal-weight PCOS subjects, who can still present with increased insulin secretion by an oral glucose tolerance test (OGTT). The evaluation of insulin secretion and resistance represents a still unresolved problem. The aim of this study is to identify a possible yet noninvasive method to properly evaluate the insulin metabolism in young non-diabetic subjects. Girls aged 14-22 years, afferent to the center of Gynecological Diseases in Childhood and Adolescence of Cagliari (Italy), were screened for PCOS. A total of 42 subjects comprised the study group. Hormonal assays, OGTT, transabdominal (TA) or transvaginal (TV) US, and urine collection for H-1-NMR analysis were assayed in the early follicular phase. A H-1-NMR coupled multivariate statistical analysis was performed. The OPLS model indicated that the NMR profile of urine had a good fit and prediction ability for the AUC OGTT with R-2 = 0.813. Metabolomics can be a promising tool to the potential identification of biomarkers of an exaggerated insulin response to OGTT and can encourage substantial progress for a more accurate and early diagnosis in PCOS.

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