血管内皮生长因子A基因多态性与伊朗人群系统性红斑狼疮易感性的关系

S. Soltani, S. Aslani, S. Faezi, A. Jamshidi, E. Farhadi, M. Mahmoudi
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引用次数: 2

摘要

背景:系统性红斑狼疮(SLE)是一种自身免疫、自身炎症性疾病,遗传因素与该病的发病机制有关。据报道,SLE患者血管内皮生长因子(VEGF)水平升高。本研究旨在评估伊朗人群中VEGFA基因rs833061和rs2010963单核苷酸多态性(snp)与SLE易感性风险的关系。方法:在这项病例对照研究中,招募了400名SLE患者和400名年龄、性别和种族匹配的健康对照者。采用实时荧光定量PCR等位基因鉴别技术对SLE患者和对照组的VEGFA基因rs833061和rs2010963多态性进行基因分型。结果:检测到rs833061和rs2010963 snp的等位基因和基因型在患者与对照组之间均无统计学差异。此外,单倍型与SLE易感性无关。而rs833061和rs2010963的多态性D = 95%为连锁不平衡,r2= 42%为非连锁不平衡。rs833061 (C vs. T: OR= 0.98, 95% CI= 0.80-1.20, P= 0.87)和rs2010963 (C vs. G: OR= 0.89, 95% CI= 0.73 - 1.09, P= 0.28)与SLE风险的相关性不显著。患者临床数据抗dsdna (P= 0.036)、抗ssa (P= 0.039)、抗ssab (P= 0.036)与VEGFA基因rs2010963 SNP基因型相关。结论:我们认识到VEGFA基因rs833061和rs2010963多态性不影响伊朗人群的SLE易感性。
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Association of Vascular Endothelial Growth Factor A gene polymorphisms with susceptibility to Systemic lupus erythematosus in Iranian population
Background: Systemic lupus erythematosus (SLE) is an autoimmune, autoinflammatory disorder in which genetic factors have been implicated in the etiopathogenesis of the disease. Elevated levels of vascular endothelial growth factor (VEGF) have been reported in patients with SLE. This study intended to evaluate the association of VEGFA gene rs833061 and rs2010963 single nucleotide polymorphisms (SNPs) with the risk of SLE susceptibility in the Iranian population.Methods: In this case-control study, 400 SLE patients and 400 age-, sex-, and ethnically-matched healthy controls were recruited. Genotyping of VEGFA gene rs833061 and rs2010963 polymorphisms in both SLE and control groups was done through the real-time PCR allelic discrimination technique.Results: It was detected that none of the alleles nor genotypes of both rs833061 and rs2010963 SNPs had a statistically significant difference between patient and control groups. Moreover, the haplotypes were not associated with the SLE susceptibility. However, rs833061 and rs2010963 polymorphisms were in linkage disequilibrium according to Dꞌ= 95 %, but not according to the r2= 42%. The associations between rs833061 (C vs. T: OR= 0.98, 95% CI= 0.80-1.20, P= 0.87) and rs2010963 (C vs. G: OR= 0.89, 95% CI= 0.73 - 1.09, P= 0.28) with risk of SLE were not significant. The clinical data of the patients, including anti-dsDNA (P= 0.036), anti-SSA (P= 0.039), and anti-SSAB (P= 0.036), were associated with the genotypes of VEGFA gene rs2010963 SNP.Conclusions: We recognize that VEGFA gene rs833061 and rs2010963 polymorphisms did not affect SLE susceptibility in the Iranian population.
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