Relationship between leptin receptor and polycystic ovary syndrome

被引:28
作者
Li, Lan [1 ]
Lee, Kyung-Ju [2 ]
Choi, Bum-Chae [3 ]
Baek, Kwang-Hyun [1 ]
机构
[1] CHA Univ, Dept Biomed Sci, Bundang CHA Hosp, Songnam 463840, Gyeonggi Do, South Korea
[2] CHA Univ, CHA Gen Hosp, Dept Gynecol & Obstet, Seoul 135081, South Korea
[3] CL Womens Hosp, Dept Obstet & Gynecol, Kwangju 502800, South Korea
关键词
Leptin; Polycystic ovary; Single nucleotide polymorphism (SNP); GENOME-WIDE ASSOCIATION; INSULIN-RESISTANCE; ADIPOSE-TISSUE; GENE POLYMORPHISMS; INCREASED RISK; OBESITY; WOMEN; METABOLISM; MUTATIONS; PROGNOSIS;
D O I
10.1016/j.gene.2013.05.074
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Polycystic ovary syndrome (PCOS) is one of the most common endocrine disorders, which is involved in the multi-system disease, and its etiology is still not clearly understood. It is currently considered that not only the genetic factors but also the environment factors play a crucial role in the pathogenesis of PCOS. Obesity plays an important role through the insulin, leptin and endocannabinoid system in the pathological process of PCOS, leading to more severe clinical manifestations. The aim of our present study is to investigate whether there is association between single nucleotide polymorphisms (SNPs) of Gln223Arg and Pro1019Pro in the leptin receptor gene (LEPR) and PCOS in a Korean population. Interestingly, a significant association was found between the Pro1019Pro in LEPR gene and PCOS, and a highly significant association was found between the Gln223Arg in LEPR gene and PCOS (P = 0.033, OR = 1.523, 95% confidence interval and P < 0.0001, OR = 0.446, 95% confidence interval). Moreover, genotype combination and haplotype analyses indicate that Gln223Arg and Pro1019Pro polymorphisms of LEPR are significantly associated with the risk of PCOS. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:71 / 74
页数:4
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