快速检测耐链霉素结核分枝杆菌rpsL基因的分子分析:一项荟萃分析。

Jing He, Baosheng Zhu, Zhaojie Yang, Binbin Hu, Lianbing Lin, Qi Zhang
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引用次数: 3

摘要

背景:耐药结核分枝杆菌(MTB)是结核病(TB)控制规划和公共卫生的主要威胁。大多数传统的药敏试验方法是精确的,但耗时。rpsL基因的分子分析具有快速、特异的特点,已广泛应用于耐链霉素结核分枝杆菌的诊断。本研究的目的是进行一项荟萃分析,以评估rpsL基因的分子测定对快速检测链霉素耐药MTB的准确性。方法:我们检索PubMed、Web of Science和EBSCO数据库,查找以常规方法为参照,应用rpsL基因分子测定法检测耐链霉素MTB的研究。采用Meta-DiSc软件建立随机效应模型,对敏感性和特异性进行汇总。采用综合受试者工作特征曲线(SROC)评价诊断的准确性。结果:共有22项研究纳入2618份标本,其中链霉素耐药标本1372份,链霉素敏感标本1246份符合纳入标准。总体敏感性和特异性估计分别为0.64(95%可信区间(CI) 0.61-0.66)和1.00 (95% CI 0.99-1.00)。SROC曲线下面积为0.9069,Cochrane (Q*)指数为0.8387。结论:本荟萃分析表明,rpsL基因的分子检测是一种可靠、有效的检测链霉素耐药MTB的方法。
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Molecular analysis of the rpsL gene for rapid detection of streptomycin-resistant Mycobacterium tuberculosis: a meta-analysis.

Background: Drug-resistant Mycobacterium tuberculosis (MTB) is a major threat to tuberculosis (TB) control programs and public health. Most conventional methods of drug susceptibility testing (DST) are precise but time-consuming. Molecular analysis of the rpsL gene has been used widely in diagnosing streptomycin-resistant MTB since it is rapid and specific. The aim of the present study was to perform a meta-analysis to assess the accuracy of molecular assay of the rpsL gene for the rapid detection of streptomycin-resistant MTB.

Methods: We searched PubMed, Web of Science, and EBSCO databases for studies that applied a molecular assay of the rpsL gene to detect streptomycin-resistant MTB with a conventional method as the reference. The sensitivity and specificity were pooled by a random effect model using Meta-DiSc software. A summary receiver operating characteristic curve (SROC) was applied to summarize the diagnostic accuracy.

Results: A total of 22 studies involving 2618 specimens with 1372 streptomycin-resistant and 1246 streptomycin-susceptible specimens met our inclusion criteria. The overall sensitivity and specificity estimates were 0.64 (95% confidence interval (CI) 0.61-0.66) and 1.00 (95% CI 0.99-1.00), respectively. The area under the SROC curve was 0.9069 and the Cochrane (Q*) index was 0.8387.

Conclusions: This meta-analysis reveals that molecular assay of the rpsL gene is a reliable and useful method for the detection of streptomycin-resistant MTB.

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