英国HIV-1基因型耐药检测绩效评估试点计划。

P A Cane, C Aitkin, K Ward, J Clarke, S Parmar, M Zuckerman, M Smith, P Tilston, S O'Shea, D Pillay
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引用次数: 0

摘要

通过基因型方法进行HIV-1药物敏感性测试现在在英国很普遍,因此确定此类调查的可重复性非常重要。进行了一项初步研究,以确定通过患者样本的核苷酸测序进行基因型检测的实验室之间的可重复性,并比较提供给临床医生的结果的解释。样品在参与的实验室之间分发。八个实验室,使用三种不同的方法,对四个样本进行了测序。核苷酸序列和报告由一个实验室进行整理和比较。在获得测序数据的地方,观察到核苷酸指定的一致性> 99%。与耐药相关的核苷酸序列未发现不一致。然而,在解释一些突变对药物敏感性的影响方面,实验室之间存在相当大的差异。这项研究强调了现有解释系统的可变性,以及在决定治疗方案时联合实验室-临床讨论的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pilot scheme for performance assessment of HIV-1 genotypic resistance testing in the UK.

HIV-1 drug susceptibility testing by genotypic methods is now widespread in the UK and it is thus important to determine the reproducibility of such investigations. A pilot study was carried out to determine the reproducibility between laboratories of genotypic testing by nucleotide sequencing of patient samples, and to compare the interpretations of the results provided to the clinicians. Samples were distributed between the participating laboratories. Eight laboratories, using three different methods, sequenced four samples. Nucleotide sequence and reports were collated and compared by one laboratory. Where sequencing data were obtained > 99% concordance was observed for nucleotide designations. No discordances in nucleotide sequencing were found in positions associated with drug resistance. However, there were considerable differences between the laboratories in the interpretation of some of the mutations with respect to their effect on drug susceptibility. This study emphasises the variability in the available interpretation systems, and the importance of joint laboratory-clinical discussion in making decisions about treatment options.

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