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Follicular hyperandrogenism and insulin resistance in polycystic ovary syndrome patients with normal circulating testosterone levels

Polycystic ovary syndrome (PCOS) is a common reproductive disease with high heterogeneity. The role of excess androgen in PCOS etiology remains disputed, since around 20%–50% of PCOS women do not display hyperandrogenemia. The microenvironment of the ovary critically influences follicular developmen...

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Autores principales: Li, Andi, Zhang, Lu, Jiang, Jiajia, Yang, Nan, Liu, Ying, Cai, Lingbo, Cui, Yugui, Diao, Feiyang, Han, Xiao, Liu, Jiayin, Sun, Yujie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Department of Journal of Biomedical Research 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6265400/
https://www.ncbi.nlm.nih.gov/pubmed/29760297
http://dx.doi.org/10.7555/JBR.32.20170136
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author Li, Andi
Zhang, Lu
Jiang, Jiajia
Yang, Nan
Liu, Ying
Cai, Lingbo
Cui, Yugui
Diao, Feiyang
Han, Xiao
Liu, Jiayin
Sun, Yujie
author_facet Li, Andi
Zhang, Lu
Jiang, Jiajia
Yang, Nan
Liu, Ying
Cai, Lingbo
Cui, Yugui
Diao, Feiyang
Han, Xiao
Liu, Jiayin
Sun, Yujie
author_sort Li, Andi
collection PubMed
description Polycystic ovary syndrome (PCOS) is a common reproductive disease with high heterogeneity. The role of excess androgen in PCOS etiology remains disputed, since around 20%–50% of PCOS women do not display hyperandrogenemia. The microenvironment of the ovary critically influences follicular development. In the present study, we assessed the role of androgen in PCOS by investigating whether excessive follicular fluid androgen was present in PCOS patients with normal serum androgen levels and influenced by follicular fluid insulin resistance (IR). Follicular fluid samples of 105 women with PCOS and 105 controls were collected. Levels of steroid hormones, glucose and insulin in the follicular fluid were examined and compared with data from serum biochemistry tests. We found that 64.9% (63/97) of PCOS patients with normal serum androgen levels displayed abnormally high follicular fluid androgen level. The follicular fluid androgen level was positively correlated with follicular fluid IR within a certain range and follicular fluid estrogen-to-testosterone (E2/T) ratio was significantly reduced in these patients. These results indicated that there existed a subgroup of PCOS patients who displayed excessive follicular fluid androgen and IR despite their normal circulating testosterone (T) levels. Our study highlights the importance of ovary hyperandrogenism and IR in the etiology of PCOS.
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spelling pubmed-62654002018-12-11 Follicular hyperandrogenism and insulin resistance in polycystic ovary syndrome patients with normal circulating testosterone levels Li, Andi Zhang, Lu Jiang, Jiajia Yang, Nan Liu, Ying Cai, Lingbo Cui, Yugui Diao, Feiyang Han, Xiao Liu, Jiayin Sun, Yujie J Biomed Res Original Article Polycystic ovary syndrome (PCOS) is a common reproductive disease with high heterogeneity. The role of excess androgen in PCOS etiology remains disputed, since around 20%–50% of PCOS women do not display hyperandrogenemia. The microenvironment of the ovary critically influences follicular development. In the present study, we assessed the role of androgen in PCOS by investigating whether excessive follicular fluid androgen was present in PCOS patients with normal serum androgen levels and influenced by follicular fluid insulin resistance (IR). Follicular fluid samples of 105 women with PCOS and 105 controls were collected. Levels of steroid hormones, glucose and insulin in the follicular fluid were examined and compared with data from serum biochemistry tests. We found that 64.9% (63/97) of PCOS patients with normal serum androgen levels displayed abnormally high follicular fluid androgen level. The follicular fluid androgen level was positively correlated with follicular fluid IR within a certain range and follicular fluid estrogen-to-testosterone (E2/T) ratio was significantly reduced in these patients. These results indicated that there existed a subgroup of PCOS patients who displayed excessive follicular fluid androgen and IR despite their normal circulating testosterone (T) levels. Our study highlights the importance of ovary hyperandrogenism and IR in the etiology of PCOS. Editorial Department of Journal of Biomedical Research 2018-06-26 2018-03-12 /pmc/articles/PMC6265400/ /pubmed/29760297 http://dx.doi.org/10.7555/JBR.32.20170136 Text en © 2018 by the Journal of Biomedical Research. All rights reserved /creativecommons.org/licenses/by/4.0/ This is an open access article under the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited.
spellingShingle Original Article
Li, Andi
Zhang, Lu
Jiang, Jiajia
Yang, Nan
Liu, Ying
Cai, Lingbo
Cui, Yugui
Diao, Feiyang
Han, Xiao
Liu, Jiayin
Sun, Yujie
Follicular hyperandrogenism and insulin resistance in polycystic ovary syndrome patients with normal circulating testosterone levels
title Follicular hyperandrogenism and insulin resistance in polycystic ovary syndrome patients with normal circulating testosterone levels
title_full Follicular hyperandrogenism and insulin resistance in polycystic ovary syndrome patients with normal circulating testosterone levels
title_fullStr Follicular hyperandrogenism and insulin resistance in polycystic ovary syndrome patients with normal circulating testosterone levels
title_full_unstemmed Follicular hyperandrogenism and insulin resistance in polycystic ovary syndrome patients with normal circulating testosterone levels
title_short Follicular hyperandrogenism and insulin resistance in polycystic ovary syndrome patients with normal circulating testosterone levels
title_sort follicular hyperandrogenism and insulin resistance in polycystic ovary syndrome patients with normal circulating testosterone levels
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6265400/
https://www.ncbi.nlm.nih.gov/pubmed/29760297
http://dx.doi.org/10.7555/JBR.32.20170136
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