首页> 外文期刊>Journal of Hepatology: The Journal of the European Association for the Study of the Liver >Predictive value of the IL28B polymorphism on the effect of interferon therapy in chronic hepatitis C patients with genotypes 2a and 2b.
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Predictive value of the IL28B polymorphism on the effect of interferon therapy in chronic hepatitis C patients with genotypes 2a and 2b.

机译:IL28B基因多态性对2a和2b基因型慢性丙型肝炎患者干扰素治疗效果的预测价值。

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BACKGROUND & AIMS: Common IL28B locus polymorphisms (SNPs rs8099917 and rs12979860) have been reported to affect peg-interferon plus ribavirin combination therapy (PEG-RBV) for hepatitis C virus (HCV) genotype 1b, but few reports have examined their effect on other two common genotypes, 2a and 2b. METHODS: We analyzed predictive factors for sustained virological response (SVR) in a retrospective study of 719 patients with either genotype 2a (530) or 2b (189). Of these patients, 160 were treated with PEG-RBV and 559 were treated with interferon monotherapy. We evaluated predictive factors including HCV RNA, histological findings, IL28B SNP genotypes (rs8099917, rs12979860, and rs12980275), and the effect of treatment regimen and prior treatment history. RESULTS: HCV RNA viral load, treatment regimen, and rs8099917 genotypes independently contributed to the effect of the therapy. For patients treated with PEG-RBV, rs8099917 and viral load were independent predictive factors for SVR in genotype 2b but not in genotype 2a. Conversely, in patients treated with interferon monotherapy, viral load and rs8099917 were independent predictive factors for SVR in genotype 2a but not in genotype 2b. The favorable rs8099917 genotype is also associated with a steep decline in viral load by the second week of treatment. CONCLUSIONS: Initial viral load and rs8099917 genotype are significant independent predictors of SVR in genotype 2 patients.
机译:背景与目的:据报道,常见的IL28B基因座多态性(SNP rs8099917和rs12979860)影响丙型肝炎病毒(HCV)基因型1b的聚乙二醇干扰素加利巴韦林联合治疗(PEG-RBV),但很少有报道检查其对其他基因的影响两种常见的基因型2a和2b。方法:在一项回顾性研究中,我们对719名2a(530)或2b(189b)基因型患者的持续病毒学应答(SVR)的预测因素进行了分析。这些患者中,有160例接受了PEG-RBV治疗,而559例接受了干扰素单药治疗。我们评估了预测因素,包括HCV RNA,组织学发现,IL28B SNP基因型(rs8099917,rs12979860和rs12980275)以及治疗方案和既往治疗史的影响。结果:HCV RNA病毒载量,治疗方案和rs8099917基因型独立影响治疗效果。对于接受PEG-RBV治疗的患者,rs8099917和病毒载量是2b型而不是2a型SVR的独立预测因素。相反,在接受干扰素单药治疗的患者中,病毒载量和rs8099917是基因型2a而非基因型2b中SVR的独立预测因素。 rs8099917基因型良好也与治疗第二周病毒载量急剧下降有关。结论:初始病毒载量和rs8099917基因型是基因2型患者SVR的重要独立预测因子。

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