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Potential genetic polymorphisms predicting polycystic ovary syndrome

Polycystic ovary syndrome (PCOS) is a heterogenous endocrine disorder with typical symptoms of oligomenorrhoea, hyperandrogenism, hirsutism, obesity, insulin resistance and increased risk of type 2 diabetes mellitus. Extensive evidence indicates that PCOS is a genetic disease and numerous biochemica...

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Autores principales: Chen, Yao, Fang, Shu-ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5937197/
https://www.ncbi.nlm.nih.gov/pubmed/29622662
http://dx.doi.org/10.1530/EC-18-0121
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author Chen, Yao
Fang, Shu-ying
author_facet Chen, Yao
Fang, Shu-ying
author_sort Chen, Yao
collection PubMed
description Polycystic ovary syndrome (PCOS) is a heterogenous endocrine disorder with typical symptoms of oligomenorrhoea, hyperandrogenism, hirsutism, obesity, insulin resistance and increased risk of type 2 diabetes mellitus. Extensive evidence indicates that PCOS is a genetic disease and numerous biochemical pathways have been linked with its pathogenesis. A number of genes from these pathways have been investigated, which include those involved with steroid hormone biosynthesis and metabolism, action of gonadotropin and gonadal hormones, folliculogenesis, obesity and energy regulation, insulin secretion and action and many others. In this review, we summarize the historical and recent findings in genetic polymorphisms of PCOS from the relevant publications and outline some genetic polymorphisms that are potentially associated with the risk of PCOS. This information could uncover candidate genes associating with PCOS, which will be valuable for the development of novel diagnostic and treatment platforms for PCOS patients.
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spelling pubmed-59371972018-05-09 Potential genetic polymorphisms predicting polycystic ovary syndrome Chen, Yao Fang, Shu-ying Endocr Connect Review Polycystic ovary syndrome (PCOS) is a heterogenous endocrine disorder with typical symptoms of oligomenorrhoea, hyperandrogenism, hirsutism, obesity, insulin resistance and increased risk of type 2 diabetes mellitus. Extensive evidence indicates that PCOS is a genetic disease and numerous biochemical pathways have been linked with its pathogenesis. A number of genes from these pathways have been investigated, which include those involved with steroid hormone biosynthesis and metabolism, action of gonadotropin and gonadal hormones, folliculogenesis, obesity and energy regulation, insulin secretion and action and many others. In this review, we summarize the historical and recent findings in genetic polymorphisms of PCOS from the relevant publications and outline some genetic polymorphisms that are potentially associated with the risk of PCOS. This information could uncover candidate genes associating with PCOS, which will be valuable for the development of novel diagnostic and treatment platforms for PCOS patients. Bioscientifica Ltd 2018-04-05 /pmc/articles/PMC5937197/ /pubmed/29622662 http://dx.doi.org/10.1530/EC-18-0121 Text en © 2018 The authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (http://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Review
Chen, Yao
Fang, Shu-ying
Potential genetic polymorphisms predicting polycystic ovary syndrome
title Potential genetic polymorphisms predicting polycystic ovary syndrome
title_full Potential genetic polymorphisms predicting polycystic ovary syndrome
title_fullStr Potential genetic polymorphisms predicting polycystic ovary syndrome
title_full_unstemmed Potential genetic polymorphisms predicting polycystic ovary syndrome
title_short Potential genetic polymorphisms predicting polycystic ovary syndrome
title_sort potential genetic polymorphisms predicting polycystic ovary syndrome
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5937197/
https://www.ncbi.nlm.nih.gov/pubmed/29622662
http://dx.doi.org/10.1530/EC-18-0121
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