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Association between TNFAIP3 Gene Polymorphisms and Risk of Allergic Rhinitis in a Chinese Han Population

机译:TNFAIP3基因多态性与中国汉族人群过敏性鼻炎风险的关系

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Tumor necrosis factor alpha-inducible protein 3 (TNFAIP3) gene polymorphisms have been reported to be associated with the susceptibility to several immune-related diseases. Here we investigated the effect of TNFAIP3 gene polymorphisms on the risk of allergic rhinitis (AR) in a Chinese Han population. The case-control study included 540 AR patients and 524 healthy controls. Genotyping for TNFAIP3 polymorphisms (rs5029928, rs9494885, rs10499194, rs610604, and rs7753873) were performed using restriction fragment length polymorphism analysis and DNA sequencing. Allele and genotype frequencies were compared between patients and controls. The rs9494885 TC genotype (corrected p (p=0.0032); odds ratio (OR)=2.06, 95% confidence intervals (CI): 1.40-3.04) and C allele (p=0.0056; OR=1.94, 95% CI: 1.35-2.76) were more frequent in AR patients compared with controls. The frequencies of the rs9494885 TT genotype (p=0.0029; OR=0.49, 95% CI: 0.33-0.72) and T allele (p= 0.0056; OR=0.52, 95% CI: 0.36-0.74) were lower in AR patients than that in controls. A higher frequency of the rs7753873 AC genotype (p=0.0023; OR=1.96, 95 %CI: 1.38-2.77) and C allele (p=0.0012; OR=1.74, 95% CI: 1.26-2.40) and a lower frequency of the rs7753873 AA genotype (p=0.0040; OR=0.53, 95% CI: 0.38-0.75) and A allele (p=0.0012; OR=0.58, 95% CI: 0.42-0.80) were observed in AR patients. TNFAIP3 gene polymorphisms (rs9494885 and rs7753873) are associated with the susceptibility to AR in the Chinese Han population.
机译:据报道肿瘤坏死因子α诱导蛋白3(TNFAIP3)基因多态性与几种免疫相关疾病的易感性有关。在这里,我们调查了中国汉族人群中TNFAIP3基因多态性对过敏性鼻炎(AR)风险的影响。病例对照研究包括540例AR患者和524例健康对照。使用限制性片段长度多态性分析和DNA测序对TNFAIP3多态性(rs5029928,rs9494885,rs10499194,rs610604和rs7753873)进行基因分型。比较患者和对照组之间的等位基因和基因型频率。 rs9494885 TC基因型(校正后的p(p = 0.0032);优势比(OR)= 2.06,95%置信区间(CI):1.40-3.04)和C等位基因(p = 0.0056; OR = 1.94,95%CI:1.35 -2.76)在AR患者中比对照组更频繁。 AR患者中rs9494885 TT基因型(p = 0.0029; OR = 0.49,95%CI:0.33-0.72)和T等位基因(p = 0.0056; OR = 0.52,95%CI:0.36-0.74)的频率低于AR患者在控件中。 rs7753873 AC基因型的较高频率(p = 0.0023; OR = 1.96,95%CI:1.38-2.77)和C等位基因(p = 0.0012; OR = 1.74,95%CI:1.26-2.40)和较低的频率在AR患者中观察到rs7753873 AA基因型(p = 0.0040; OR = 0.53,95%CI:0.38-0.75)和A等位基因(p = 0.0012; OR = 0.58,95%CI:0.42-0.80)。 TNFAIP3基因多态性(rs9494885和rs7753873)与中国汉族人群对AR的易感性有关。

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