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E-选择素基因(SEL-E)中的 rs1805193、rs5361 和 rs5355 单核苷酸多态性与亚临床动脉粥样硬化相关:动脉粥样硬化疾病的遗传学(GEA)墨西哥研究。

The rs1805193, rs5361, and rs5355 single nucleotide polymorphisms in the E-selectin gene (SEL-E) are associated with subclinical atherosclerosis: The Genetics of Atherosclerotic Disease (GEA) Mexican study.

机构信息

Department of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.

Department of Endocrinology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico.

出版信息

Immunobiology. 2019 Jan;224(1):10-14. doi: 10.1016/j.imbio.2018.11.003. Epub 2018 Nov 24.

DOI:10.1016/j.imbio.2018.11.003
PMID:30501958
Abstract

The aim of this study was to evaluate the association of rs1805193, rs5361, and rs5355 E-selectin gene single nucleotide polymorphisms (SNPs) with the risk of developing subclinical atherosclerosis (SA) in a group of Mexicans individuals. SNPs were determined by TaqMan genotyping assays in a group of 287 individuals with SA and 688 healthy controls. Under different models, the T allele of the 5'UTR G98 T (rs1805193) (OR = 1.71, 95%CI: 1.00-2.93, pC = 0.0006, OR = 2.02, 95%CI: 1.21-3.38, pC = 0.004, and OR = 2.14, 95%CI: 1.34-3.44, pC = 0.0015) and the C allele of the Ser128Arg A561C (rs5361) (OR = 1.60, 95%CI: 0.92-2.79, pC = 0.012, OR = 1.78, 95%CI: 1.04-3.06, pC = 0.038, and OR = 1.87, 95%CI: 1.13-3.11, pC = 0.016) polymorphisms were associated with an increased risk of development of SA. In the same way, under co-dominant model, the CT genotype of the Leu575Phe C1880T (rs5355) polymorphism was associated with an increased risk of SA as compared to CC genotype (OR = 2.34, 95%CI: 1.33-4.11, pC = 0.0035). All models were adjusted by traditional cardiovascular risk factors. In summary, this study demonstrates that the 5'UTR G98 T, Ser128Arg A561C, and Leu575Phe C1880T polymorphisms are associated with an increased risk of developing SA.

摘要

本研究旨在评估 rs1805193、rs5361 和 rs5355 E-选择素基因单核苷酸多态性 (SNP) 与一组墨西哥个体发生亚临床动脉粥样硬化 (SA) 的风险之间的关联。在一组 287 名 SA 患者和 688 名健康对照中,通过 TaqMan 基因分型检测 SNP。在不同模型下,5'UTR G98→T (rs1805193) 的 T 等位基因 (OR=1.71, 95%CI: 1.00-2.93, pC=0.0006, OR=2.02, 95%CI: 1.21-3.38, pC=0.004, 和 OR=2.14, 95%CI: 1.34-3.44, pC=0.0015) 和 Ser128Arg A561C 的 C 等位基因 (rs5361) (OR=1.60, 95%CI: 0.92-2.79, pC=0.012, OR=1.78, 95%CI: 1.04-3.06, pC=0.038, 和 OR=1.87, 95%CI: 1.13-3.11, pC=0.016) 多态性与 SA 发病风险增加相关。同样,在共显性模型下,与 CC 基因型相比,Leu575Phe C1880T (rs5355) 多态性的 CT 基因型与 SA 的发生风险增加相关 (OR=2.34, 95%CI: 1.33-4.11, pC=0.0035)。所有模型均通过传统心血管危险因素进行调整。总之,本研究表明,5'UTR G98→T、Ser128Arg A561C 和 Leu575Phe C1880T 多态性与 SA 的发生风险增加相关。

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