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首页> 外文期刊>Journal of Medical Virology >Predictive value of early viral dynamics during peginterferon and ribavirin combination therapy based on genetic polymorphisms near the IL28B gene in patients infected with HCV genotype 1b.
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Predictive value of early viral dynamics during peginterferon and ribavirin combination therapy based on genetic polymorphisms near the IL28B gene in patients infected with HCV genotype 1b.

机译:基于IL28B基因附近的遗传多态性,聚乙二醇干扰素和利巴韦林联合治疗期间早期病毒动力学对HCV基因型1b感染患者的预测价值。

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A study was carried out to determine whether early viral dynamics retain prediction of the outcome of peginterferon (PEG-IFN) and ribavirin combination therapy based on different genetic polymorphisms near the IL28B gene, the strongest baseline predictor of response to this therapy. A total of 272 patients infected with hepatitis C virus (HCV) genotype 1b were grouped according to genetic polymorphisms near the IL28B gene (rs8099917). The ability of reduced HCV RNA levels at 4 and 12 weeks after starting therapy to predict a sustained virologic response was evaluated based on these genotypes. Among patients with the TT genotype for rs8099917 (associated with a favorable response), the rates of sustained virologic response were higher in patients with a >/=3 log(10) reduction in serum HCV RNA levels at 4 weeks after starting therapy (P < 0.0001). In contrast, among patients with the TG/GG genotype (associated with an unfavorable response), there were no differences in this rate based on the reduction in HCV RNA levels at 4 weeks. Early viral dynamics at 4 weeks after starting therapy retains its predictive value for sustained virologic response in patients with the TT genotype for rs8099917, but not in patients with the TG/GG genotype. Patients who are likely to achieve sustained virologic response despite unfavorable TG/GG genotype cannot be identified based on early viral dynamics during therapy. In contrast, lack of early virologic response at 12 weeks retains a strong predictive value for the failure of sustained virologic response regardless of IL28B polymorphisms, which remains useful as a factor to stop therapy.
机译:进行了一项研究,以根据IL28B基因附近不同的遗传多态性来确定早期病毒动力学是否保留了聚乙二醇干扰素(PEG-IFN)和利巴韦林联合治疗的结果预测,IL28B基因是该治疗反应的最强基线预测因子。根据接近IL28B基因的遗传多态性(rs8099917),将总共272名感染了丙型肝炎病毒(HCV)基因型1b的患者分组。基于这些基因型,评估了开始治疗后第4周和第12周HCV RNA水平降低的能力,以预测持续的病毒学应答。在具有rs8099917 TT基因型的患者(与良好的应答相关)中,开始治疗后4周血清HCV RNA水平降低> / = 3 log(10)的患者的持续病毒学应答率更高(P <0.0001)。相反,在TG / GG基因型(与不良反应相关)的患者中,基于4周时HCV RNA水平的降低,该比率没有差异。开始治疗后4周的早期病毒动力学对于rs基因型为rs8099917的患者保持持续的病毒学应答仍具有预测价值,而对于TG / GG基因型的患者则没有。尽管TG / GG基因型不利,仍可能实现持续病毒学应答的患者无法根据治疗期间的早期病毒动力学进行鉴定。相反,不管IL28B多态性如何,缺乏持续12周的早期病毒学应答仍对持续病毒学应答失败具有很强的预测价值,而IL28B多态性仍可作为终止治疗的一个因素。

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