结核病与肺部健康杂志 ›› 2013, Vol. 2 ›› Issue (2): 112-114.

• 论著 • 上一篇    下一篇

荧光定量PCR和双抗原夹心胶体金免疫层析法检测结核分枝杆菌的对比观察

梁少碧   

  1. 528500 广东省佛山市高明区慢性病防治站内科综合呼吸专科
  • 收稿日期:2013-03-04 出版日期:2013-06-30 发布日期:2013-06-30

Comparative study for detecting Mycobacterium tuberculosis with methods of fluorogenic quantitative PCR and double antigen sandwich colloidal gold immunochromatography

LIANG Shao-bi   

  1. Department of Internal Medicine Respiratory Specialist,Institute of Chronic Disease Prevention and Control of Gaoming District,Foshan,Guangdong,Foshan 528500,China
  • Received:2013-03-04 Online:2013-06-30 Published:2013-06-30

摘要: 目的比较荧光定量PCR和双抗原夹心胶体金免疫层析法检测结核分枝杆菌的诊断价值。方法选取经过结核分枝杆菌培养阳性的70例肺结核患者,分别采取荧光定量PCR和双抗原夹心胶体金免疫层析法进行结核分枝杆菌的检测,观察比较两种检测法的敏感度、特异度及准确率。采用SPSS 12.0软件处理数据,以P<0.05为差异有统计学意义。结果以细菌培养结果作为金标准,双抗原夹心胶体金免疫层析法与荧光定量PCR法检测结果进行比较,前者检测假阳性率明显低于后者[前者:1.7%(1/59),后者:8.8%(6/68);χ2=5.46,P<0.05],即前者特异度较高;前者检测假阴性率明显高于后者[前者:15.7%(11/70),后者:2.9%(2/70);χ2=9.71,P<0.05],即后者敏感度较高;两种检测方法的结果准确率比较差异无统计学意义[前者:82.9%(58/70),后者:88.6%(62/70);χ2=1.33,P>0.05]。结论两种检测方法皆是临床上迅速检测结核分枝杆菌的有效方法,其中荧光定量PCR敏感度高,应用在初筛中效果更为显著,而双抗原夹心胶体金免疫层析法特异度高,可进一步作为鉴别诊断的参考依据,各有利弊,可结合临床实际需要合理选用。

Abstract: Objective To compare the diagnostic value of detecting Mycobacterium tuberculosis(Mtb)with fluorogenic quantitative PCR(polymerase chain reaction)and double antigen sandwich colloidal gold immunochromatography.Methods Seventy cases with culture-positive pulmonary tuberculosis were selected to compare the sensitivities,specificities and accuracies of fluorogenic quantitative PCR and double antigen sandwich colloidal gold immunochromatography respectively. SPSS 12.0 software was applied for data cleaning and analysis,and P<0.05 was set as the criteria of statistical significance.Results The bacterial culture results were regarded as the gold stan-dard, the results of fluorogenic quantitative PCR(the former)and double antigen sandwich colloidal gold immunochromatography(the latter)were compared. The false-positive rate of the former was significantly lower than the latter [the former:1.7%(1/59),the latter:8.8%(6/68). χ2=5.46,P<0.05]. It meant the specificity of the former was relative higher. The false-negative rate of the former was significantly higher than the latter [the former:15.7%(11/70),the latter:2.9%(2/70). χ2=9.71,P<0.05]. The sensitivity of the latter was higher. There was no statistical significance of the difference between the accuracies of the two methods [the former:82.9%(58/70),the latter:88.6%(62/70). χ2=1.33,P>0.05].Conclusion Both methods are effective and rapid clinical methods to detect Mtb. The fluorogenic quantitative PCR has a more remarkable effect in primary screening with its higher sensitivity, and the double antigen sandwich colloidal gold immunochromatography technique can be a reference for diffe-rential diagnosis with its higher specificity. Both of them have advantages and disadvantages,and they should be selected according to the clinical practice.