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白细胞介素-17基因变异在中国汉族女性子痫前期中的作用

Role of IL-17 Variants in Preeclampsia in Chinese Han Women.

作者信息

Wang Haiyan, Guo Mingzhen, Liu Fenghua, Wang Jingli, Zhou Zheng, Ji Jing, Ye Yuanhua, Song Weiqing, Liu Shiguo, Sun Bo

机构信息

Department of Blood Transfusion, the Affiliated Hospital of Qingdao University, Qingdao, China.

Department of Blood Transfusion, the First Affiliated Hospital of Harbin Medical University, Harbin, China.

出版信息

PLoS One. 2015 Oct 9;10(10):e0140118. doi: 10.1371/journal.pone.0140118. eCollection 2015.

Abstract

Previous studies have suggested an important role for IL-17, mainly secreted by Th17 cells, in the development of systemic inflammation in preeclampsia (PE). This study therefore investigated the association between genetic variants in IL-17A, IL-17F, and IL-17RA and susceptibility to PE in Chinese Han women. We recruited 1,031 PE patients and 1,298 controls of later pregnant women, and used TaqMan allelic discrimination real-time PCR to genotype the polymorphisms of IL17A rs2275913, IL-17F rs763780, and IL-17RA rs4819554. No significant differences in genotypic or allelic frequencies were found at all three polymorphic sites between PE patients and controls (rs2275913: genotype χ2 = 0.218, p = 0.897 and allele χ2 = 0.157, p = 0.692, OR = 1.024, 95%CI 0.911-1.152; rs763780: genotype χ2 = 1.948, p = 0.377 and allele χ2 = 1.242, p = 0.265, OR = 0.897, 95%CI 0.741-1.086; rs4819554: genotype χ2 = 0.633, p = 0.729 and allele χ2 = 0.115, p = 0.735, OR = 1.020, 95%CI 0.908-1.146). There were also no significant differences in genetic distributions between mild/severe PE or early/late-onset PE and control subgroups. Our data indicate that the genetic variants of rs2275913 in IL-17A, rs763780 in IL-17F, and rs4819554 in IL-17RA may not play a role in the pathogenesis of PE in Chinese Han women. However, these findings should be confirmed in other ethnic populations.

摘要

以往研究表明,主要由Th17细胞分泌的白细胞介素-17(IL-17)在子痫前期(PE)全身炎症反应的发生发展中起重要作用。因此,本研究调查了IL-17A、IL-17F和IL-17RA基因变异与中国汉族女性患PE易感性之间的关联。我们招募了1031例PE患者和1298例晚期妊娠女性作为对照,采用TaqMan等位基因鉴别实时荧光定量PCR技术对IL17A rs2275913、IL-17F rs763780和IL-17RA rs4819554的多态性进行基因分型。在PE患者和对照组之间,所有三个多态性位点的基因型或等位基因频率均无显著差异(rs2275913:基因型χ2 = 0.218,p = 0.897,等位基因χ2 = 0.157,p = 0.692,OR = 1.024,95%CI 0.911 - 1.152;rs763780:基因型χ2 = 1.948,p = 0.377,等位基因χ2 = 1.242,p = 0.265,OR = 0.897,95%CI 0.741 - 1.086;rs4819554:基因型χ2 = 0.633,p = 0.729,等位基因χ2 = 0.115,p = 0.735,OR = 1.020,95%CI 0.908 - 1.146)。轻度/重度PE或早发型/晚发型PE与对照组亚组之间的基因分布也无显著差异。我们的数据表明,IL-17A中的rs2275913、IL-17F中的rs763780和IL-17RA中的rs4819554基因变异可能在中国汉族女性PE发病机制中不起作用。然而,这些发现应在其他种族人群中得到证实。

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