Servicio Microbiología Clínica, Complejo Hospitalario Navarra, Pamplona, Spain; Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain; CIBER Epidemiología y Salud Pública (CIBERESP), Spain.
Servicio Microbiología Clínica, Complejo Hospitalario Navarra, Pamplona, Spain; Instituto de Investigación Sanitaria de Navarra (IdiSNA), Pamplona, Spain.
Int J Infect Dis. 2019 Dec;89:131-136. doi: 10.1016/j.ijid.2019.09.022. Epub 2019 Sep 30.
New efficient strategies are needed for the assessment of active hepatitis C virus (HCV) infection. The aim of this study was to evaluate the ability of HCV core antigen (HCV-cAg) as a marker of active HCV infection in newly diagnosed patients, for treatment monitoring, and for the detection of therapeutic failure.
A prospective study was conducted at a regional reference hospital in Spain. HCV-cAg and viral load (RNA-HCV) were tested in plasma or serum samples from three patient groups: new diagnosis, treatment monitoring, and treatment failure. The treatment monitoring group was tested at the beginning of treatment, at 4 weeks post-initiation, at the end of treatment, and at 12 weeks post-treatment completion. The Architect HCV core antigen assay was performed for HCV-cAg testing, and viral load was quantified with the Cobas 6800 system.
A total of 303 samples from 124 patients were analyzed. Excellent correlation was seen between HCV-cAg and HCV-RNA (R=0.932). The optimal cut-off value was 3fmol/l in the receiver operating characteristics curve analysis, and the area under the curve was 0.987 (95% confidence interval 0.972-1.000). HCV-cAg sensitivity and specificity were 97% and 95%, respectively. Most diverging results were observed in the treatment follow-up group.
HCV-cAg demonstrated good sensitivity and specificity as a marker for active HCV infection, new diagnosis, detection of antiviral therapeutic failure, and treatment monitoring.
需要新的有效策略来评估丙型肝炎病毒(HCV)的活跃感染。本研究旨在评估 HCV 核心抗原(HCV-cAg)作为新诊断患者活跃 HCV 感染、治疗监测和检测治疗失败的标志物的能力。
在西班牙一家地区参考医院进行了一项前瞻性研究。在三组患者的血浆或血清样本中检测 HCV-cAg 和病毒载量(RNA-HCV):新诊断、治疗监测和治疗失败。治疗监测组在治疗开始时、治疗开始后 4 周、治疗结束时和治疗完成后 12 周进行检测。使用 Architect HCV 核心抗原检测试剂盒进行 HCV-cAg 检测,使用 Cobas 6800 系统定量病毒载量。
共分析了来自 124 名患者的 303 个样本。HCV-cAg 与 HCV-RNA 之间存在极好的相关性(R=0.932)。在受试者工作特征曲线分析中,最佳截断值为 3fmol/l,曲线下面积为 0.987(95%置信区间 0.972-1.000)。HCV-cAg 的灵敏度和特异性分别为 97%和 95%。在治疗随访组中观察到的结果差异最大。
HCV-cAg 作为活跃 HCV 感染、新诊断、抗病毒治疗失败检测和治疗监测的标志物,具有良好的灵敏度和特异性。