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The correlation of aromatase activity and obesity in women with or without polycystic ovary syndrome
BACKGROUND: This study aimed to investigate the effect of polycystic ovary syndrome (PCOS) on the association of aromatase activity assessed by estradiol-to-testosterone ratio (E(2)/T) with body mass index (BMI) in women. METHODS: This was a cohort study in five centers for reproductive medicine in...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392749/ https://www.ncbi.nlm.nih.gov/pubmed/25881575 http://dx.doi.org/10.1186/s13048-015-0139-1 |
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author | Chen, Jie Shen, Shanmei Tan, Yong Xia, Dong Xia, Yanjie Cao, Yunxia Wang, Wenjun Wu, Xiaoke Wang, Hongwei Yi, Long Gao, Qian Wang, Yong |
author_facet | Chen, Jie Shen, Shanmei Tan, Yong Xia, Dong Xia, Yanjie Cao, Yunxia Wang, Wenjun Wu, Xiaoke Wang, Hongwei Yi, Long Gao, Qian Wang, Yong |
author_sort | Chen, Jie |
collection | PubMed |
description | BACKGROUND: This study aimed to investigate the effect of polycystic ovary syndrome (PCOS) on the association of aromatase activity assessed by estradiol-to-testosterone ratio (E(2)/T) with body mass index (BMI) in women. METHODS: This was a cohort study in five centers for reproductive medicine in China. Data were collected from July 2012 to December 2013. PCOS patients (n = 785) and non PCOS, healthy, age-matched controls (n = 297) were included. Plasma sex hormones including estradiol (E(2)), testosterone (T), follicle stimulating hormone (FSH), and luteinizing hormone (LH) were measured by ELISA, together with BMI and E(2)/T being calculated, on the third day of the menstrual cycle. Aromatase activity in PCOS patients with different BMI, T and E(2) levels were compared. RESULTS: E(2)/T was significantly lower (P < 0.05) while BMI was significantly increased (P < 0.05) in PCOS than non-PCOS. No significant difference was observed in E(2)/T among different BMI subgroups of either PCOS or control. Ovarian aromatase activity was decreased in PCOS patients which was independent of BMI. Hyperestrogen promoted ovarian aromatase activity, while hyperandrogen inhibited such activity, both in a dose-dependent, biphasic manner. CONCLUSIONS: Ovarian aromatase activity was lower in PCOS, which was independent of BMI. New therapeutic strategies can be developed by targeting aromatase activity for treating PCOS women, especially those with obesity. |
format | Online Article Text |
id | pubmed-4392749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43927492015-04-11 The correlation of aromatase activity and obesity in women with or without polycystic ovary syndrome Chen, Jie Shen, Shanmei Tan, Yong Xia, Dong Xia, Yanjie Cao, Yunxia Wang, Wenjun Wu, Xiaoke Wang, Hongwei Yi, Long Gao, Qian Wang, Yong J Ovarian Res Research BACKGROUND: This study aimed to investigate the effect of polycystic ovary syndrome (PCOS) on the association of aromatase activity assessed by estradiol-to-testosterone ratio (E(2)/T) with body mass index (BMI) in women. METHODS: This was a cohort study in five centers for reproductive medicine in China. Data were collected from July 2012 to December 2013. PCOS patients (n = 785) and non PCOS, healthy, age-matched controls (n = 297) were included. Plasma sex hormones including estradiol (E(2)), testosterone (T), follicle stimulating hormone (FSH), and luteinizing hormone (LH) were measured by ELISA, together with BMI and E(2)/T being calculated, on the third day of the menstrual cycle. Aromatase activity in PCOS patients with different BMI, T and E(2) levels were compared. RESULTS: E(2)/T was significantly lower (P < 0.05) while BMI was significantly increased (P < 0.05) in PCOS than non-PCOS. No significant difference was observed in E(2)/T among different BMI subgroups of either PCOS or control. Ovarian aromatase activity was decreased in PCOS patients which was independent of BMI. Hyperestrogen promoted ovarian aromatase activity, while hyperandrogen inhibited such activity, both in a dose-dependent, biphasic manner. CONCLUSIONS: Ovarian aromatase activity was lower in PCOS, which was independent of BMI. New therapeutic strategies can be developed by targeting aromatase activity for treating PCOS women, especially those with obesity. BioMed Central 2015-03-22 /pmc/articles/PMC4392749/ /pubmed/25881575 http://dx.doi.org/10.1186/s13048-015-0139-1 Text en © Chen et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Chen, Jie Shen, Shanmei Tan, Yong Xia, Dong Xia, Yanjie Cao, Yunxia Wang, Wenjun Wu, Xiaoke Wang, Hongwei Yi, Long Gao, Qian Wang, Yong The correlation of aromatase activity and obesity in women with or without polycystic ovary syndrome |
title | The correlation of aromatase activity and obesity in women with or without polycystic ovary syndrome |
title_full | The correlation of aromatase activity and obesity in women with or without polycystic ovary syndrome |
title_fullStr | The correlation of aromatase activity and obesity in women with or without polycystic ovary syndrome |
title_full_unstemmed | The correlation of aromatase activity and obesity in women with or without polycystic ovary syndrome |
title_short | The correlation of aromatase activity and obesity in women with or without polycystic ovary syndrome |
title_sort | correlation of aromatase activity and obesity in women with or without polycystic ovary syndrome |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4392749/ https://www.ncbi.nlm.nih.gov/pubmed/25881575 http://dx.doi.org/10.1186/s13048-015-0139-1 |
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