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Tumor necrosis factor-alpha microsatellite polymorphism association with rheumatoid arthritis in Indian patients.

机译:肿瘤坏死因子-α微卫星多态性与类风湿关节炎的印度患者。

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BACKGROUND: Level of TNF-alpha increases significantly in synovial fluid of rheumatoid arthritis (RA) patients. It is proposed that tumor necrosis factor (TNF) microsatellite alleles may influence its expression and presumably can contribute to the disease severity. However, there is a lack of such study to predict any such association with RA in an Indian population. METHODS: In this study, we investigated the differential pattern of distribution of TNF microsatellite alleles in an Indian population and its association with RA. One hundred eighteen RA patients and 120 healthy individuals were genotyped for TNF microsatellite alleles using Genescan. Odds ratio was calculated to demonstrate the correlation between allelic distribution and clinical severity. RESULTS: The study shows that distribution of TNF microsatellite alleles in an Indian population is very different from other Asian Oriental and Western populations, except for some similarities with an Italian population. Frequency of microsatelliteTNFd3 allele (9.24 vs. 3.85%, chi(2)=5.6, p < or =0.0179, OR=0.393, 95% CI=0.177-0.87) and more interestingly TNFd3 containing haplotypes has been found significantly reduced in patients. On the contrary, TNFb5 allele frequency increased in the patients (22.3 vs. 30.8%, chi(2)=4.4, p < or =0.036, OR=1.55, 95% CI=1.027-2.344) as compared to controls. Furthermore, significant increase in frequency of this allele in severe patients (22.3 vs. 33.8%, chi(2)=6.22, p < or =0.013, OR=1.78, 95% CI=1.132-2.798) along with the significant increase in haplotypes containing this allele supports the association of TNFb5 with disease severity. CONCLUSIONS: In an Indian population, TNFb5 may be considered as a risk factor, whereas TNFd3, unlike others, may be protective for RA.
机译:背景:类风湿关节炎(RA)患者的滑液中TNF-α水平显着增加。有人提出,肿瘤坏死因子(TNF)微卫星等位基因可能影响其表达,并可能导致疾病严重。但是,缺乏这样的研究来预测印度人口中与RA的任何这种关联。方法:在这项研究中,我们调查了印度人群中TNF微卫星等位基因分布的差异模式及其与RA的关系。使用Genescan对118位RA患者和120位健康个体的TNF微卫星等位基因进行基因分型。计算几率以证明等位基因分布与临床严重性之间的相关性。结果:研究表明,除了与意大利人群的某些相似之处外,印度人群中TNF微卫星等位基因的分布与其他亚洲东方和西方人群有很大差异。微卫星TNFd3等位基因的频率(9.24 vs.3.85%,chi(2)= 5.6,p <或= 0.0179,OR = 0.393,95%CI = 0.177-0.87)和更有趣的是发现患者中含有TNFd3的单倍型。相反,与对照组相比,患者的TNFb5等位基因频率增加(22.3对30.8%,chi(2)= 4.4,p <或= 0.036,OR = 1.55,95%CI = 1.027-2.344)。此外,重症患者中该等位基因频率的显着增加(22.3 vs. 33.8%,chi(2)= 6.22,p <或= 0.013,OR = 1.78,95%CI = 1.132-2.798),以及包含该等位基因的单倍型支持TNFb5与疾病严重程度的关联。结论:在印度人群中,TNFb5可能被认为是危险因素,而TNFd3与其他人群不同,可能对RA具有保护作用。

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