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HCV Ag quantification as a one-step procedure in diagnosing chronic hepatitis C infection in Cameroon: the ANRS 12336 study

机译:HCV Ag定量作为诊断喀麦隆慢性丙型肝炎感染的一站式程序:ANRS 12336研究

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>Introduction: The diagnostic procedure for chronic hepatitis C infection (CHC) usually combines anti-HCV antibody (HCV-Ab) and HCV-RNA measurement. Quantifying HCV core antigen (cAg) as a one-step procedure could shorten the diagnostic process. We aimed to assess the performance of cAg quantification in diagnosing CHC and how it is influenced by concomitant HIV or HBV infections.>Methods: The cAg was quantified by an automated assay (Abbott Diagnostics) in 465 HCV-Ab negative serum samples and 544 HCV-RNA positive serum samples (n = 1009) collected in patients from the Pasteur Center in Cameroon, some of whom were infected by HBV or HIV. Its performance was evaluated in comparison to the gold standard (ELISA or PCR) by estimating its sensitivity (Se) and specificity (Sp), and by comparing the area under ROC (AUROC) curves in each patient population: HCV mono-infected, HCV-HBV and HIV-HCV co-infected.>Results: Among the 465 HCV-Ab negative patients, 51 and 79 were HIV- and HBV-infected, respectively, whereas among the 544 patients with CHC, 27 and 28 were HIV- and HBV-infected, respectively. The Spearman ρ correlation coefficient between cAg and HCV-RNA was 0.75 (p < 0.00001). The assay had a sensitivity of 95.7% (95% CI: 93.2–97.5) and a specificity of 99.7% (95% CI: 98.1–10) in diagnosing CHC, corresponding to an AUROC of 0.99 (95% CI: 0.98–1.0). Being HIV- or HBV-infected did not impact the performance of cAg (Se = 96.4%, Sp = 96.2% and AUROC = 0.98 (95% CI: 0.95–1.0) in the HBV group, Se = 100%, Sp = 88.2% and AUROC = 0.99 (95% CI: 0.97–1.0) in the HIV group, p between AUROC = 0.69).>Conclusions: The cAg quantification displayed a high specificity and sensitivity for the diagnosis of CHC in Cameroon, and its performance was not significantly modified by a concomitant HIV or HBV infection. In the context of CHC elimination on a global scale, using cAg quantification as a screening tool to directly identify CHC could be a reliable tool in a “test and treat” strategy.
机译:>简介:慢性丙型肝炎(CHC)的诊断程序通常结合抗HCV抗体(HCV-Ab)和HCV-RNA测量。一步定量HCV核心抗原(cAg)可以缩短诊断过程。我们旨在评估cAg定量在诊断CHC中的性能以及它如何受到伴随的HIV或HBV感染的影响。>方法:通过自动测定法(Abbott Diagnostics)在465 HCV-Ab中对cAg进行定量从喀麦隆巴斯德中心的患者中收集了阴性血清样本和544例HCV-RNA阳性血清样本(n = 1009),其中一些感染了HBV或HIV。通过评估其灵敏度(Se)和特异性(Sp),并通过比较每个患者群体的ROC下面积(AUROC)曲线,与黄金标准(ELISA或PCR)进行比较,评估其性能:HCV单感染,HCV >结果:在465例HCV-Ab阴性患者中,分别有51和79例被HIV和HBV感染,而在544例CHC患者中,有27例和28分别是HIV和HBV感染。 cAg与HCV-RNA之间的Spearmanρ相关系数为0.75(p <0.00001)。该方法在诊断CHC中的敏感性为95.7%(95%CI:93.2–97.5),特异性为99.7%(95%CI:98.1–10),对应于AUROC为0.99(95%CI:0.98–1.0) )。在HBV组中,被HIV或HBV感染不会影响cAg(Se = 96.4%,Sp = 96.2%和AUROC = 0.98(95%CI:0.95–1.0))的表现,Se = 100%,Sp = 88.2 HIV组中的%和AUROC = 0.99(95%CI:0.97–1.0),p在AUROC = 0.69之间。>结论:cAg定量显示对CHC的诊断具有很高的特异性和敏感性。喀麦隆,其性能并未因伴随的HIV或HBV感染而显着改变。在全球范围内消除CHC的背景下,使用cAg定量作为筛查工具直接识别CHC可能是“测试与治疗”策略中的可靠工具。

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