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分子诊断中的即时检测(POCT):GeneXpert HCV RNA检测在丙型肝炎病毒感染诊断和监测中的性能评估

Point -of -care testing (POCT) in molecular diagnostics: Performance evaluation of GeneXpert HCV RNA test in diagnosing and monitoring of HCV infection.

作者信息

Gupta Ekta, Agarwala Pragya, Kumar Guresh, Maiwall Rakhi, Sarin Shiv Kumar

机构信息

Department of Clinical Virology, Institute of Liver & Biliary Sciences (ILBS), Vasant Kunj, New Delhi 110070, India.

Department of Clinical Virology, Institute of Liver & Biliary Sciences (ILBS), Vasant Kunj, New Delhi 110070, India.

出版信息

J Clin Virol. 2017 Mar;88:46-51. doi: 10.1016/j.jcv.2017.01.006. Epub 2017 Jan 29.

Abstract

BACKGROUND

Molecular testing at the point-of-care may turn out to be game changer for HCV diagnosis and treatment monitoring, through increased sensitivity, reduced turnaround time, and ease of performance. One such assay GeneXpert has recently been released.

OBJECTIVES

Comparative analysis between performances of GeneXpert and Abbott HCV-RNA was done.

STUDY DESIGN

174 HCV infected patients were recruited and, one time plasma samples from 154 patients and repeated samples from 20 patients, obtained at specific treatment time-points (0, 4, 12 and 24) weeks were serially re-tested on Xpert.

RESULTS

Genotype 3 was the commonest, seen in 80 (66%) of the cases, genotype 1 in 34 (28.3%), genotype 4 in 4 (3.3%) and genotypes 2 and 5 in 1 (0.8%) each. Median HCV RNA load was 4.69 log (range: 0-6.98log) IU/ml. Overall a very good correlation was seen between the two assays (R=0.985), concordance of the results between the assays was seen in 138 samples (89.6%). High and low positive standards were tested ten times on Xpert to evaluate the precision and the coefficient of variation was 0.01 for HPC and 0.07 for the LPC. Monitoring of patients on two different regimes of treatment, pegylated interferon plus ribavirin and sofosbuvir plus ribavirin was done by both the systems at baseline, 4, 12 and 24 weeks. Perfect correlation between the assays in the course of therapy at different treatment time- point in genotypes 3 and 1 was seen.

CONCLUSION

The study demonstrates excellent performance of the Xpert HCV assay in viral load assessment and in treatment course monitoring consistency.

摘要

背景

即时检验的分子检测可能会成为丙型肝炎病毒(HCV)诊断和治疗监测的变革者,因为它具有更高的灵敏度、更短的周转时间且操作简便。最近已推出了一种这样的检测方法——GeneXpert。

目的

对GeneXpert和雅培HCV-RNA的性能进行比较分析。

研究设计

招募了174例HCV感染患者,从154例患者中获取一次血浆样本,并从20例患者中获取在特定治疗时间点(0、4、12和24周)的重复样本,在GeneXpert上进行连续重新检测。

结果

基因型3最为常见,在80例(66%)病例中出现,基因型1在34例(28.3%)中出现,基因型4在4例(3.3%)中出现,基因型2和5各在1例(0.8%)中出现。HCV RNA载量中位数为4.69 log(范围:0 - 6.98 log)IU/ml。总体而言,两种检测方法之间具有非常好的相关性(R = 0.985),138个样本(89.6%)的检测结果具有一致性。在GeneXpert上对高、低阳性标准品进行了10次检测以评估精密度,高阳性标准品的变异系数为0.01,低阳性标准品的变异系数为0.07。两种检测系统在基线、4、12和24周时对接受聚乙二醇干扰素加利巴韦林和索磷布韦加利巴韦林两种不同治疗方案的患者进行了监测。在基因型3和1的不同治疗时间点的治疗过程中,两种检测方法之间呈现出完美的相关性。

结论

该研究证明了GeneXpert HCV检测在病毒载量评估和治疗过程监测一致性方面具有出色的性能。

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