Chen Yao, Fang Shu-Ying
Hangzhou Fuyang Women and Children HospitalHangzhou, China
Hangzhou Fuyang Women and Children HospitalHangzhou, China.
Endocr Connect. 2018 May;7(5):R187-R195. doi: 10.1530/EC-18-0121. Epub 2018 Apr 5.
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.
多囊卵巢综合征(PCOS)是一种异质性内分泌疾病,具有月经过少、高雄激素血症、多毛、肥胖、胰岛素抵抗以及2型糖尿病风险增加等典型症状。大量证据表明,PCOS是一种遗传性疾病,众多生化途径与其发病机制相关。已对这些途径中的许多基因进行了研究,其中包括参与类固醇激素生物合成与代谢、促性腺激素和性腺激素作用、卵泡发生、肥胖与能量调节、胰岛素分泌与作用等的基因。在本综述中,我们总结了相关出版物中关于PCOS基因多态性的历史和最新研究结果,并概述了一些可能与PCOS风险相关的基因多态性。这些信息可能揭示与PCOS相关的候选基因,这对于开发针对PCOS患者的新型诊断和治疗平台具有重要价值。