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丙型肝炎病毒核心抗原作为直接作用抗病毒药物治疗后评估治疗效果的一种可能替代方法。

Hepatitis C virus core antigen as a possible alternative for evaluation of treatment effectiveness after treatment with direct-acting antivirals.

作者信息

Łucejko M, Tomasiewicz K, Olczak A, Tudrujek-Zdunek M, Halota W, Jelski W, Donica H, Krintus M, Mroczko B, Flisiak R

机构信息

Department of Infectious Diseases and Hepatology, Medical University of Bialystok, Bialystok, Poland.

Department of Infectious Diseases and Hepatology, Division of Laboratory Diagnostics, Medical University of Lublin, Lublin, Poland.

出版信息

Br J Biomed Sci. 2019 Oct;76(4):190-194. doi: 10.1080/09674845.2019.1654790. Epub 2019 Sep 6.

Abstract

: Chronic hepatitis C is a major public health problem around the world. In monitoring treatment efficacy, although costly and labour-intensive methods of molecular biology are often used, much cheaper and technically easier serological methods evaluating the concentration of HCV core antigen in serum are available. We evaluated HCVcAg quantification as a possible assessment of the treatment efficacy instead of HCV RNA quantification.: We collected 514 serum samples from treated HCV infected patients. Quantitative evaluation of HCV RNA and HCVcAg was carried out before treatment, at the end of treatment, and at least 12 weeks following treatment termination. HCV RNA was determined by automated assay (Roche COBAS) and HCVcAg quantitation with ARCHITECT ci8200 analyser.: There was a significant correlation between HCVcAg and HCV RNA concentrations at baseline and follow-up visits, but not at the end of treatment. Among samples collected before the treatment, at the end of treatment and follow-up visit, concordance of HCV RNA and HCVcAg reached level of 98.1%, 98.9% and 98.7%, respectively. Diagnostic sensitivity, specificity, positive and negative predictive values of HCVcAg detection were >97%.: HCVcAg measurement could be an alternative for determining HCV treatment efficacy after chemotherapy and could be an option in the diagnosis of HCV infection.

摘要

慢性丙型肝炎是全球主要的公共卫生问题。在监测治疗效果时,虽然常使用成本高且耗费人力的分子生物学方法,但也有更便宜且技术上更简便的血清学方法可用于评估血清中丙型肝炎病毒(HCV)核心抗原的浓度。我们评估了HCVcAg定量作为一种可能的治疗效果评估方法,以替代HCV RNA定量。

我们收集了514例接受治疗的HCV感染患者的血清样本。在治疗前、治疗结束时以及治疗终止后至少12周对HCV RNA和HCVcAg进行定量评估。HCV RNA通过自动化检测(罗氏COBAS)测定,HCVcAg定量使用ARCHITECT ci8200分析仪。

在基线和随访时,HCVcAg与HCV RNA浓度之间存在显著相关性,但在治疗结束时不存在。在治疗前、治疗结束时和随访时收集的样本中,HCV RNA和HCVcAg的一致性分别达到98.1%、98.9%和98.7%。HCVcAg检测的诊断敏感性、特异性、阳性和阴性预测值均>97%。

HCVcAg测量可作为化疗后确定HCV治疗效果的替代方法,也可作为HCV感染诊断的一种选择。

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