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白细胞介素-31基因多态性与中国人群隐睾症风险的关联

Association of Interleukin-31 gene polymorphisms with risk of cryptorchidism in a Chinese population.

作者信息

Zou Bing, Yu Zhihai, Huang Jing, Tan Chunlin, Wang Haiyun, Fu Jian, Li Xin, Wang Xiaojun, Cui Shu, Tang Tielong

机构信息

Department of Urology.

Urogenital Diseases Lab, Affiliated Hospital of North Sichuan Medical College, Nanchong.

出版信息

Medicine (Baltimore). 2019 May;98(22):e15861. doi: 10.1097/MD.0000000000015861.

Abstract

This study aims to investigate the possible association between Interleukin-31 (IL-31) gene polymorphisms and cryptorchidism risk.Two single nucleotide polymorphisms of IL-31, rs7977932 (C/G) and rs4758680 (C/A), were selected to be investigated in this study. Polymerase chain reaction-restriction fragment length polymorphism methods were used to discriminate the selected single nucleotide polymorphisms of IL-31 gene. A hospital-based case-control study of 112 cryptorchidism patients and 425 healthy controls was conducted.The frequencies of the C allele of rs4758680 in the patients with cryptorchidism were significantly higher compared with those in controls (89% vs 83%, P = .02, OR = 0.58, 95% CI = 0. 37-0.92). Compared with CC genotype in dominant model, notable decreased frequencies of A carriers (CA/AA genotypes) were observed in cryptorchidism patients (P = . 03, OR = 0.58, 95% CI = 0.35-0.96).Results demonstrated that IL-31 gene polymorphisms were associated with the genetic susceptibility to cryptorchidism in a Chinese population. Compared with CC genotype, the A carriers (CA/AA genotypes) of rs4758680 were protect factors in cryptorchidism susceptibility.

摘要

本研究旨在探讨白细胞介素-31(IL-31)基因多态性与隐睾症风险之间的可能关联。本研究选择了IL-31的两个单核苷酸多态性,即rs7977932(C/G)和rs4758680(C/A)进行研究。采用聚合酶链反应-限制性片段长度多态性方法来鉴别所选的IL-31基因单核苷酸多态性。开展了一项基于医院的病例对照研究,纳入112例隐睾症患者和425例健康对照。与对照组相比,隐睾症患者中rs4758680的C等位基因频率显著更高(89%对83%,P = 0.02,OR = 0.58,95%CI = 0.37 - 0.92)。在显性模型中,与CC基因型相比,隐睾症患者中A携带者(CA/AA基因型)的频率显著降低(P = 0.03,OR = 0.58,95%CI = 0.35 - 0.96)。结果表明,IL-31基因多态性与中国人群隐睾症的遗传易感性相关。与CC基因型相比,rs4758680的A携带者(CA/AA基因型)是隐睾症易感性的保护因素。

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