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Comparison clinical and metabolic effects of metformin and pioglitazone in polycystic ovary syndrome

INTRODUCTION: Polycystic ovary syndrome (PCOS) is one of the most common endocrine disorders in women. PCOS comprises a broad spectrum of anomalies, including hyperandrogenism, chronic anovulation, obesity, and infertility. Insulin resistance and its compensatory hyperinsulinemia play a key role in...

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Autores principales: Shahebrahimi, Karoon, Jalilian, Nasrin, Bazgir, Nasrin, Rezaei, Mansour
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5105565/
https://www.ncbi.nlm.nih.gov/pubmed/27867884
http://dx.doi.org/10.4103/2230-8210.192925
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author Shahebrahimi, Karoon
Jalilian, Nasrin
Bazgir, Nasrin
Rezaei, Mansour
author_facet Shahebrahimi, Karoon
Jalilian, Nasrin
Bazgir, Nasrin
Rezaei, Mansour
author_sort Shahebrahimi, Karoon
collection PubMed
description INTRODUCTION: Polycystic ovary syndrome (PCOS) is one of the most common endocrine disorders in women. PCOS comprises a broad spectrum of anomalies, including hyperandrogenism, chronic anovulation, obesity, and infertility. Insulin resistance and its compensatory hyperinsulinemia play a key role in the pathogenicity of PCOS. This study compares the effects of 2 types of insulin sensitizer drugs, metformin and pioglitazone, on clinical, metabolic, and endocrine characteristics of women with PCOS. METHODS: In this randomized clinical trial, 56 women with PCOS (ages 20–49 years) were treated orally with either metformin (500 mg 3 times daily) or pioglitazone (30 mg daily) for 3 months. Clinical (body weight, blood pressure [BP], and body mass index) and laboratory indices (fasting blood sugar [FBS], serum triglyceride [TG], cholesterol, low-density lipoprotein, high-density lipoprotein, insulin, testosterone, and dehydroepiandrosterone [DHEA]) were measured before and after therapy. Data were analyzed by Chi-square and McNemar's tests. RESULTS: Significant decreases were seen after treatment with metformin in extent of hair loss (P = 0.008), wrist circle (P = 0.011), weight (P = 0.047), diastolic BP (P = 0.023), and DHEA (P = 0.035). A significant decrease in TG was seen with pioglitazone treatment (P = 0.047). In both groups, significant decreases in acne, menstrual disturbance, FBS, and serum insulin were seen. CONCLUSION: There is a significant amelioration of endocrine and metabolic indices with pioglitazone in PCOS patients. Although we were not able to recommend one treatment regime over the other, pioglitazone offers a useful, alternate treatment in women with PCOS who are not able to tolerate metformin.
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spelling pubmed-51055652016-11-18 Comparison clinical and metabolic effects of metformin and pioglitazone in polycystic ovary syndrome Shahebrahimi, Karoon Jalilian, Nasrin Bazgir, Nasrin Rezaei, Mansour Indian J Endocrinol Metab Original Article INTRODUCTION: Polycystic ovary syndrome (PCOS) is one of the most common endocrine disorders in women. PCOS comprises a broad spectrum of anomalies, including hyperandrogenism, chronic anovulation, obesity, and infertility. Insulin resistance and its compensatory hyperinsulinemia play a key role in the pathogenicity of PCOS. This study compares the effects of 2 types of insulin sensitizer drugs, metformin and pioglitazone, on clinical, metabolic, and endocrine characteristics of women with PCOS. METHODS: In this randomized clinical trial, 56 women with PCOS (ages 20–49 years) were treated orally with either metformin (500 mg 3 times daily) or pioglitazone (30 mg daily) for 3 months. Clinical (body weight, blood pressure [BP], and body mass index) and laboratory indices (fasting blood sugar [FBS], serum triglyceride [TG], cholesterol, low-density lipoprotein, high-density lipoprotein, insulin, testosterone, and dehydroepiandrosterone [DHEA]) were measured before and after therapy. Data were analyzed by Chi-square and McNemar's tests. RESULTS: Significant decreases were seen after treatment with metformin in extent of hair loss (P = 0.008), wrist circle (P = 0.011), weight (P = 0.047), diastolic BP (P = 0.023), and DHEA (P = 0.035). A significant decrease in TG was seen with pioglitazone treatment (P = 0.047). In both groups, significant decreases in acne, menstrual disturbance, FBS, and serum insulin were seen. CONCLUSION: There is a significant amelioration of endocrine and metabolic indices with pioglitazone in PCOS patients. Although we were not able to recommend one treatment regime over the other, pioglitazone offers a useful, alternate treatment in women with PCOS who are not able to tolerate metformin. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC5105565/ /pubmed/27867884 http://dx.doi.org/10.4103/2230-8210.192925 Text en Copyright: © Indian Journal of Endocrinology and Metabolism http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Shahebrahimi, Karoon
Jalilian, Nasrin
Bazgir, Nasrin
Rezaei, Mansour
Comparison clinical and metabolic effects of metformin and pioglitazone in polycystic ovary syndrome
title Comparison clinical and metabolic effects of metformin and pioglitazone in polycystic ovary syndrome
title_full Comparison clinical and metabolic effects of metformin and pioglitazone in polycystic ovary syndrome
title_fullStr Comparison clinical and metabolic effects of metformin and pioglitazone in polycystic ovary syndrome
title_full_unstemmed Comparison clinical and metabolic effects of metformin and pioglitazone in polycystic ovary syndrome
title_short Comparison clinical and metabolic effects of metformin and pioglitazone in polycystic ovary syndrome
title_sort comparison clinical and metabolic effects of metformin and pioglitazone in polycystic ovary syndrome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5105565/
https://www.ncbi.nlm.nih.gov/pubmed/27867884
http://dx.doi.org/10.4103/2230-8210.192925
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