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使用2周内病毒反应预测基于替拉那韦的三联疗法的持续病毒学应答

Prediction of Sustained Virological Response to Telaprevir-Based Triple Therapy Using Viral Response within 2 Weeks.

作者信息

Tamai Hideyuki, Shimizu Ryo, Shingaki Naoki, Mori Yoshiyuki, Maeshima Shuya, Nuta Junya, Maeda Yoshimasa, Moribata Kosaku, Muraki Yosuke, Deguchi Hisanobu, Inoue Izumi, Maekita Takao, Iguchi Mikitaka, Kato Jun, Ichinose Masao

机构信息

Second Department of Internal Medicine, Wakayama Medical University, 811-1 Kimiidera, Wakayama, Wakayama Prefecture 641-0012, Japan.

出版信息

Hepat Res Treat. 2014;2014:748935. doi: 10.1155/2014/748935. Epub 2014 Sep 28.

Abstract

The aim of the present study was to predict sustained virological response (SVR) to telaprevir with pegylated interferon (PEG-IFN) and ribavirin using viral response within 2 weeks after therapy initiation. Thirty-six patients with genotype 1 hepatitis C virus (HCV) and high viral load were treated by telaprevir-based triple therapy. SVR was achieved in 72% (26/36) of patients. Significant differences between the SVR group and non-SVR group were noted regarding response to prior PEG-IFN plus ribavirin, interleukin (IL)28B polymorphism, amino acid substitution at core 70, cirrhosis, hyaluronic acid level, and HCV-RNA reduction within 2 weeks. Setting 4.56 logIU/mL as the cut-off value for HCV-RNA reduction at 2 weeks, the sensitivity, specificity, positive predictive value, negative predictive value, and accuracy for predicting SVR were 77%, 86%, 95%, 50%, and 79%, respectively, and for neither the IL28B minor allele nor core 70 mutant were 80%, 71%, 91%, 50%, and 78%, respectively. In conclusion, evaluation of viral reduction at 2 weeks or the combination of IL28B polymorphism and amino acid substitution at core 70 are useful for predicting SVR to telaprevir with PEG-IFN and ribavirin therapy.

摘要

本研究的目的是利用治疗开始后2周内的病毒反应,预测特拉匹韦联合聚乙二醇干扰素(PEG-IFN)和利巴韦林治疗的持续病毒学应答(SVR)。36例基因1型丙型肝炎病毒(HCV)且病毒载量高的患者接受了基于特拉匹韦的三联疗法。72%(26/36)的患者实现了SVR。在对既往PEG-IFN加利巴韦林的反应、白细胞介素(IL)28B多态性、核心区70位氨基酸替代、肝硬化、透明质酸水平以及2周内HCV-RNA降低情况方面,SVR组和非SVR组之间存在显著差异。将2周时HCV-RNA降低的截断值设定为4.56 logIU/mL,预测SVR的敏感性、特异性、阳性预测值、阴性预测值和准确性分别为77%、86%、95%、50%和79%,对于IL28B次要等位基因和核心区70位突变体,相应的值分别为80%、71%、91%、50%和78%。总之,评估2周时的病毒降低情况或IL28B多态性与核心区70位氨基酸替代的组合,对于预测特拉匹韦联合PEG-IFN和利巴韦林治疗的SVR是有用的。

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