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用于乙肝病毒DNA定量的Versant HBV DNA 3.0检测法与COBAS AmpliPrep - COBAS TaqMan检测法的比较:可能的临床意义。

Comparison of Versant HBV DNA 3.0 and COBAS AmpliPrep-COBAS TaqMan assays for hepatitis B DNA quantitation: Possible clinical implications.

作者信息

Garbuglia A R, Angeletti C, Lauria F N, Zaccaro P, Cocca A M, Pisciotta M, Solmone M, Capobianchi M R

机构信息

Laboratory of Virology, National Institute of Infectious Diseases INMI, Lazzaro Spallanzani, Via Portuense, 292-00149 Rome, Italy.

出版信息

J Virol Methods. 2007 Dec;146(1-2):274-80. doi: 10.1016/j.jviromet.2007.07.005. Epub 2007 Aug 20.

Abstract

We compared two commercial assays for HBV DNA quantitation, Versant HBV 3.0, System 340 (bDNA; Bayer Diagnostics) and COBAS AmpliPrep-COBAS TaqMan HBV Test (TaqMan; Roche Diagnostics). Analytical sensitivity, calculated on WHO International Standard, predicted 95% detection rate at 11.4 and 520.2IU/ml for TaqMan and bDNA, respectively. Specificity, established on 50 blood donor samples, was 100% and 84% for TaqMan and bDNA, respectively. When using clinical samples, HBV DNA was detected by TaqMan in 21/55 samples negative to bDNA. Mean values of HBV DNA obtained with bDNA were higher than those obtained with TaqMan (4.09log(10)+/-1.90 versus 3.39log(10)+/-2.41, p<0.001), and 24.4% of samples showed differences in viral load values >0.5log(10), without association with HBV genotype. There was a good correlation for HBV DNA concentrations measured by the two assays (r=0.94; p<0.001) within the overlapping range, and the distribution of results with respect to relevant clinical threshold recently confirmed (20,000 and 2000IU/ml) was similar. Approximately 50% of samples with low HBV DNA, appreciated by TaqMan but not by bDNA, were successfully sequenced in pol region, where drug resistance mutations are located.

摘要

我们比较了两种用于乙肝病毒(HBV)DNA定量的商业检测方法,即Versant HBV 3.0系统340(分支DNA法;拜耳诊断公司)和COBAS AmpliPrep - COBAS TaqMan HBV检测法(TaqMan法;罗氏诊断公司)。根据世界卫生组织国际标准计算得出的分析灵敏度显示,TaqMan法和分支DNA法在11.4IU/ml和520.2IU/ml时的预测检测率分别为95%。在50份献血者样本上确定的特异性方面,TaqMan法和分支DNA法分别为100%和84%。使用临床样本时,TaqMan法在55份分支DNA法检测为阴性的样本中检测出21份存在HBV DNA。分支DNA法获得的HBV DNA平均值高于TaqMan法(4.09log₁₀±1.90对3.39log₁₀±2.41,p<0.001),并且24.4%的样本病毒载量值差异>0.5log₁₀,与HBV基因型无关。两种检测方法在重叠范围内测量的HBV DNA浓度具有良好的相关性(r = 0.94;p<0.001),并且关于最近确认的相关临床阈值(20,000和2000IU/ml)的结果分布相似。大约50%的低HBV DNA样本,TaqMan法检测到但分支DNA法未检测到,在耐药突变所在的pol区域成功进行了测序。

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