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首页> 外文期刊>Rheumatology International >Association of tumor necrosis factor alpha and IL-10 promoter polymorphisms with rheumatoid arthritis in North Indian population
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Association of tumor necrosis factor alpha and IL-10 promoter polymorphisms with rheumatoid arthritis in North Indian population

机译:肿瘤坏死因子α和IL-10启动子多态性与北印度人类风湿关节炎的关联

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摘要

Rheumatoid arthritis is a chronic autoimmune disorder associated with altered expression of pro- and anti-inflammatory cytokines in the affected tissues. The aim of this study was to investigate the association between promoter polymorphisms of TNFα and IL-10 gene with susceptibility, age of disease onset and disease severity in North Indian patients with rheumatoid arthritis (RA). SNPs at position −308 and −863 of TNF gene and −819/−592 and −1082 position of IL-10 gene were determined in 222 patients and 208 healthy controls using RFLP or ARMS method. Polymorphism TNF −308A was less prevalent among the patients (1.7%) than controls (4.9%; p = 0.01, OR: 0.32, 95% CI: 0.13–0.76). Among female patients, IL-10 −592A allele associated with higher baseline disease activity scores (5.77 ± 1.99) than −592C (5.57 ± 1.19; p = 0.04). Female patients carrying allele A of TNFα −863 had earlier age of onset of RA (33.99 ± 9.6 years) than those with allele C (36.15 ± 11.21 years; p = 0.043). In conclusion, allele A at TNFα −308 locus provides protection against RA in North Indian population while another TNF allele A at −863 position had weak association with earlier onset of disease in female patients. On the other hand promoter polymorphisms of IL-10 did not affect susceptibility but polymorphism at −819/−592A was associated with higher disease activity scores at baseline.
机译:类风湿关节炎是一种慢性自身免疫性疾病,与受影响的组织中促炎和抗炎细胞因子的表达改变有关。这项研究的目的是调查北印度类风湿关节炎(RA)患者的TNFα和IL-10基因启动子多态性与易感性,疾病发作年龄和疾病严重程度之间的关系。使用RFLP或ARMS方法在222例患者和208名健康对照中测定了TNF基因的-308和-863位以及IL-10基因的-819 / -592和-1082位的SNP。多态性TNF -308A在患者(1.7%)中比对照组(4.9%; p = 0.01,OR:0.32,95%CI:0.13-0.76)少。在女性患者中,IL-10 -592A等位基因与-592C(5.57±1.19; p = 0.04)相关的基线疾病活动评分更高(5.77±1.99)。携带TNFα-863等位基因A的女性患者的RA发病年龄(33.99±9.6岁)比等位基因C的女性(36.15±11.21岁; p = 0.043)更早。总之,在TNFα-308位点的等位基因A为北印度人群提供了针对RA的保护,而在-863位的另一个TNF等位基因A与女性患者疾病的早期发作之间存在弱关联。另一方面,IL-10的启动子多态性不会影响药敏性,但在-819 / -592A处的多态性与基线时较高的疾病活动性评分相关。

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