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首页> 外文期刊>Journal of Clinical Microbiology >Effect of Multiple Freeze-Thaw Cycles on Hepatitis B Virus DNA and Hepatitis C Virus RNA Quantification as Measured with Branched-DNA Technology
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Effect of Multiple Freeze-Thaw Cycles on Hepatitis B Virus DNA and Hepatitis C Virus RNA Quantification as Measured with Branched-DNA Technology

机译:支链DNA技术测量多个冻融循环对乙型肝炎病毒DNA和丙型肝炎病毒RNA定量的影响

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摘要

Quantification of hepatitis B virus (HBV) DNA and hepatitis C virus (HCV) RNA often is performed in specimens that have been frozen and thawed more than once. To ensure optimal therapeutic and prognostic value, it is important to establish whether viral load measurements are affected by repeated freeze-thaw (FT) cycles. We therefore evaluated the effect of multiple FT cycles on HBV DNA and HCV RNA quantification by testing serum specimens subjected to one (baseline), two, four, and eight FT cycles with the appropriate Chiron Quantiplex assay. Linear regression analysis showed minor increases of 1.7% per FT cycle for both HBV DNA and HCV RNA. The rise in HCV RNA levels was more pronounced among low-concentration samples, since further analysis revealed an increase of 3.2% per FT cycle among samples with 0.2 to 3.86 Meq of HCV RNA per ml. Given that the coefficient of variation for the Quantiplex assays is generally 10 to 15%, the minor increases in HBV DNA and HCV RNA levels with progressive FT cycles for the specimens tested were recognized only because analysis of variance revealed a statistically significant trend (P < 0.05). Due to the minor statistical trend, the clinical impact for individual patient specimens is likely to be limited, but it may deserve further study. In conclusion, the concentration of HBV DNA and HCV RNA in serum specimens subjected to up to eight short-term FT cycles was stable.
机译:乙型肝炎病毒(HBV)DNA和丙型肝炎病毒(HCV)RNA的定量通常在已经多次冷冻和融化的标本中进行。为了确保最佳的治疗和预后价值,重要的是要确定病毒载量的测量是否受到重复的冻融(FT)周期的影响。因此,我们通过使用适当的Chiron Quantiplex测定法检测经过一个(基线),两个,四个和八个FT循环的血清样本,评估了多个FT循环对HBV DNA和HCV RNA定量的影响。线性回归分析显示,对于HBV DNA和HCV RNA,每个FT周期仅增加1.7%。 HCV RNA水平的升高在低浓度样品中更为明显,因为进一步的分析显示,每毫升HCV RNA含量为0.2至3.86 Meq的样品中,每个FT循环增加3.2%。鉴于Quantiplex分析的变异系数通常为10%到15%,因此仅在进行方差分析后发现统计学上的显着趋势( P <0.05)。由于统计趋势较小,对单个患者标本的临床影响可能有限,但值得进一步研究。总之,血清标本中的HBV DNA和HCV RNA的浓度经过最多八个短期FT循环后是稳定的。

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