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作 者:于霞[1,2] 梁倩[1,2] 马异峰[1,2] 付育红[1,2] 黄海荣[1,2]
机构地区:[1]北京市结核病胸部肿瘤研究所 [2]首都医科大学附属北京胸科医院,北京101149
出 处:《中国实验诊断学》2013年第5期846-849,共4页Chinese Journal of Laboratory Diagnosis
基 金:北京市重大科技攻关项目(D121100003012001)
摘 要:目的评价环介导等温扩增技术(loop-mediated isothermal amplification,LAMP)技术在结核分枝杆菌诊断中的应用价值。方法收集246份疑似肺结核患者的痰标本,分别进行涂片镜检,罗氏培养以及实时定量PCR和LAMP法检测。结果涂片镜检,罗氏培养实时定量PCR和LAMP法对结核分枝杆菌的检出率分别为30.89%,45.53%,54.47%,57.32%。以罗氏培养结果作为金标准,LAMP法诊断的敏感性为96.19%(101/105),特异性为76.87%(103/134),两种方法检测结果的一致性是Κ=0.71,两法具有很好的吻合性。以实时定量法为标准,LAMP法的敏感性为90.07%(127/141),特异性为93.33%(98/105),两法检测结果的一致性是κ=0.83,P<0.001。结论 LAMP法检测结核分枝杆菌具有较高的敏感性和特异性,与罗氏培养和RT-PCR有着较高的吻合性,很适合作为临床检测项目开展。Objective To evaluate the diagnostic value of loop-mediated isothermal amplification(LAMP)in the diag nosis of Mycobacterium tuberculosis. Methods Collected 246 sputa from suspected tuberculosis patients and conducted smear microscopy,IJ culture,real-time quantitative PCR (RT-PCR)and LAMP assay. Results The detection rate of smear microscopy, LJ culture, RT-PCR and LAMP assay for Mycobacterium tuberculosis were 30. 89%, 45. 53%, 54.47% and 57.32%, respectively. Comparing with culture method, the sensitivity and the specificity of the LAMP assay was 96. 19% (101/105) and 76. 87% (103/134), respectively. The two assays were in good consistency (K= 0.71). Comparing with RT-PCR,the sensitivity and specificity of the LAMP was 90.07% (127/141) and 93.33%(98/ 105), respectively. The two assays were in good consistency(K=0.83) . Conclusion LAMP assay for rapid detection of Mycobacterium tuberculosis with high sensitivity and specificity,has high consistency with culture and RT-PCR,and is very suitable for routine clinical test.
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