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The clinical characteristics and etiological study of nonalcoholic fatty liver disease in Chinese women with PCOS

Background: Polycystic ovary syndrome (PCOS) is highly associated with non-alcoholic fatty liver disease (NAFLD). There are extensive ethnic differences in the clinical manifestations, pathological changes, and ovarian changes in women with PCOS. Objective: To investigate the prevalence and clinical...

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Autores principales: Qu, Zhongyu, Zhu, Yanhui, Jiang, Jingjing, Shi, Yuhua, Chen, Zijiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research and Clinical Center for Infertility 2013
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941330/
https://www.ncbi.nlm.nih.gov/pubmed/24639812
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author Qu, Zhongyu
Zhu, Yanhui
Jiang, Jingjing
Shi, Yuhua
Chen, Zijiang
author_facet Qu, Zhongyu
Zhu, Yanhui
Jiang, Jingjing
Shi, Yuhua
Chen, Zijiang
author_sort Qu, Zhongyu
collection PubMed
description Background: Polycystic ovary syndrome (PCOS) is highly associated with non-alcoholic fatty liver disease (NAFLD). There are extensive ethnic differences in the clinical manifestations, pathological changes, and ovarian changes in women with PCOS. Objective: To investigate the prevalence and clinical characteristics of NAFLD in Chinese women with PCOS. Materials and Methods: Non-pregnant women with PCOS (N= 602) and matched controls without PCOS (N=588) were recruited. Basal endocrine, oral glucose tolerance test, insulin release level, lipid level, blood pressure, and body mass index (BMI) were measured. Liver biochemical and B-hepatitis and C-hepatitis indices were determined. Results: NAFLD was significantly more prevalent in women with PCOS than controls (32.9% vs. 18.5%) and included 113 (57.1%) mild, 75 (37.8%) moderate and 10 (5.1%) severe cases. Luteinizing hormone was significantly lower in PCOS women with NAFLD than without NAFLD. In the PCOS group, NAFLD prevalence and severity increased with BMI. The liver index was significantly higher (p<0.001), and the quantitative insulin sensitivity check index and high density lipoprotein cholesterol were significantly lower (p<0.001) in the PCOS group than controls. Insulin resistance, abdominal obesity, diabetes mellitus, abnormal glucose tolerance, liver dysfunction, dyslipidemia, hypertension, and metabolic syndrome were significantly more prevalent in the NAFLD group than controls. Conclusion: Chinese women with PCOS have a high prevalence of mostly mild and moderate NAFLD, not significantly associated with hyperandrogenism that increased significantly with BMI. Insulin resistance and metabolic abnormalities are important factors associated with NAFLD. Chinese women with BMI ≥24 kg/m(2) should be screened for NAFLD.
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spelling pubmed-39413302014-03-17 The clinical characteristics and etiological study of nonalcoholic fatty liver disease in Chinese women with PCOS Qu, Zhongyu Zhu, Yanhui Jiang, Jingjing Shi, Yuhua Chen, Zijiang Iran J Reprod Med Background: Polycystic ovary syndrome (PCOS) is highly associated with non-alcoholic fatty liver disease (NAFLD). There are extensive ethnic differences in the clinical manifestations, pathological changes, and ovarian changes in women with PCOS. Objective: To investigate the prevalence and clinical characteristics of NAFLD in Chinese women with PCOS. Materials and Methods: Non-pregnant women with PCOS (N= 602) and matched controls without PCOS (N=588) were recruited. Basal endocrine, oral glucose tolerance test, insulin release level, lipid level, blood pressure, and body mass index (BMI) were measured. Liver biochemical and B-hepatitis and C-hepatitis indices were determined. Results: NAFLD was significantly more prevalent in women with PCOS than controls (32.9% vs. 18.5%) and included 113 (57.1%) mild, 75 (37.8%) moderate and 10 (5.1%) severe cases. Luteinizing hormone was significantly lower in PCOS women with NAFLD than without NAFLD. In the PCOS group, NAFLD prevalence and severity increased with BMI. The liver index was significantly higher (p<0.001), and the quantitative insulin sensitivity check index and high density lipoprotein cholesterol were significantly lower (p<0.001) in the PCOS group than controls. Insulin resistance, abdominal obesity, diabetes mellitus, abnormal glucose tolerance, liver dysfunction, dyslipidemia, hypertension, and metabolic syndrome were significantly more prevalent in the NAFLD group than controls. Conclusion: Chinese women with PCOS have a high prevalence of mostly mild and moderate NAFLD, not significantly associated with hyperandrogenism that increased significantly with BMI. Insulin resistance and metabolic abnormalities are important factors associated with NAFLD. Chinese women with BMI ≥24 kg/m(2) should be screened for NAFLD. Research and Clinical Center for Infertility 2013-09 /pmc/articles/PMC3941330/ /pubmed/24639812 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Qu, Zhongyu
Zhu, Yanhui
Jiang, Jingjing
Shi, Yuhua
Chen, Zijiang
The clinical characteristics and etiological study of nonalcoholic fatty liver disease in Chinese women with PCOS
title The clinical characteristics and etiological study of nonalcoholic fatty liver disease in Chinese women with PCOS
title_full The clinical characteristics and etiological study of nonalcoholic fatty liver disease in Chinese women with PCOS
title_fullStr The clinical characteristics and etiological study of nonalcoholic fatty liver disease in Chinese women with PCOS
title_full_unstemmed The clinical characteristics and etiological study of nonalcoholic fatty liver disease in Chinese women with PCOS
title_short The clinical characteristics and etiological study of nonalcoholic fatty liver disease in Chinese women with PCOS
title_sort clinical characteristics and etiological study of nonalcoholic fatty liver disease in chinese women with pcos
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941330/
https://www.ncbi.nlm.nih.gov/pubmed/24639812
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