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作 者:徐爱芳[1] 陈刚[1] 王妙婵[1] 朱秀亚[1]
机构地区:[1]浙江中医药大学附属杭州市第六人民医院,杭州310014
出 处:《中国卫生检验杂志》2009年第10期2337-2338,共2页Chinese Journal of Health Laboratory Technology
摘 要:目的:采用时间分辨免疫荧光法(TRFIA法)检测乙肝患者前S1抗原,并与酶联免疫吸附法(ELISA法)测定的前S1抗原结果及HBV-DNA测定结果进行比较。方法:分别采用TRFIA法和ELISA法检测362例乙肝患者血清标本的前S1抗原,并进行卡方检验比较。对两种乙肝病毒前S1抗原检测方法结果不符合的标本和部分前S1抗原检测结果在Cutoff值附近的标本进行HBV-DNA的定量检测,并作比较。结果:以ELISA法为参考,TRFIA法的阳性符合率为98.8%,阴性符合率为75.7%,总体符合率为92.0%,两种检测方法的差异有统计学意义(χ2=16.69,P<0.01),TRFIA法的检测阳性率高于ELISA法。与乙肝病毒DNA检测结果相比,TRFIA法差异无统计学意义(χ2=0.25,P>0.05),ELISA法差异有统计学意义(χ2=19.36,P<0.01)。结论:与ELISA法相比,采用TRFIA法检测前S1抗原能更好地反映病人体内乙肝病毒复制情况。Objective: Using time - resolved immunofluorescence assay (TRFIA) to detect hepatitis B patients pre - S1 antigen and comparing the results of enzyme - linked immunosorbent assay (ELISA) and HBV - DNA measured results. Methods: TRFIA method and ELISA method were used separately to detect serum pre - S1 antigen of 362 cases of hepatitis B patients. HBV - DNA was detected to the specimens which PreS1 antigen results did not meet by two methods and some pre - S1 antigen test results are near Cutoff. Results : Using the ELISA method as a reference, the positive coincidence rate of TRFIA method was 98. 8% and the negative coincidence rate was 75.7%. The overall coincidence rate was 92.0% and the difference between the two methods had statistical significance. The positive rate of TRFIA method was higher than ELISA method. Comprised With hepatitis B virus DNA results. The TRFIA method had no significant difference. And the ELISA method had statistical significance. Conclusion:Compared with the ELISA method, detection of pre S1 antigen with TRFIA method can better reflect the hepatitis B virus replication.
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