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Confirmation of -174G/C interleukin-6 gene promoter polymorphism as a genetic marker predicting antitumor necrosis factor treatment outcome

机译:确认-174G / C白细胞介素6基因启动子多态性作为预测抗肿瘤坏死因子治疗结果的遗传标记

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BACKGROUND: The IL-6 -174G/C genetic variant has recently been associated with the clinical response to etanercept therapy in rheumatoid arthritis (RA) patients. Considering previous results, the aim of our study was to validate the role of this polymorphism as a predictor of the antitumor necrosis factor (anti-TNF) treatment outcome in RA. MATERIALS AND METHODS: Our study population was composed of 199 Spanish patients with RA receiving anti-TNF therapy. The IL-6 -174G/C (rs1800795) genetic variant was genotyped using the TaqMan allelic discrimination technology. Patients were classified, according to the European League Against Rheumatism (EULAR) criteria, as responders (good and moderate response) and nonresponders at 6, 12, 18, and 24 months after the first infusion. RESULTS: The -174 G allele was significantly associated with a good or moderate EULAR response at 12 [P=0.015, odds ratio (OR)=2.93, 95% confidence interval (CI) 1.29-6.70], 18 (P=4.54E-03, OR=5.17, 95% CI 1.80-14.85), and 24 months (P=4.54E-03, OR=14.86, 95% CI 2.91-75.91). A meta-analysis combining these data with the results from a previous study confirmed this association (P=1.89E-02, OR=1.80, 95% CI 1.13-2.87, at 12 months). CONCLUSION: Our results support the role of the -174G/C IL-6 polymorphism as a genetic marker of responsiveness to anti-TNF therapy.
机译:背景:IL-6 -174G / C基因变异最近与类风湿关节炎(RA)患者对依那西普治疗的临床反应有关。考虑到以前的结果,我们的研究目的是验证这种多态性作为RA中抗肿瘤坏死因子(anti-TNF)治疗结果的预测指标的作用。材料与方法:我们的研究人群由199名接受抗TNF治疗的西班牙RA患者组成。使用TaqMan等位基因鉴别技术对IL-6 -174G / C(rs1800795)遗传变异进行基因分型。根据欧洲抗风湿病联盟(EULAR)的标准,在首次输注后的6、12、18和24个月,将患者分为反应者(良好和中度反应)和无反应者。结果:-174 G等位基因与12时的良好或中等EULAR反应显着相关[P = 0.015,优势比(OR)= 2.93,95%置信区间(CI)1.29-6.70],18(P = 4.54E -03,OR = 5.17,95%CI 1.80-14.85)和24个月(P = 4.54E-03,OR = 14.86,95%CI 2.91-75.91)。荟萃分析将这些数据与先前研究的结果相结合,证实了这种关联(P = 1.89E-02,OR = 1.80,95%CI 1.13-2.87,在12个月时)。结论:我们的结果支持-174G / C IL-6多态性作为抗TNF治疗反应的遗传标志物的作用。

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