HBV DNA与HBVm对比分析
乙型肝炎病毒;,脱氧核糖核酸;,荧光定量聚合酶链反应;,血清标志物;,酶联免疫吸附试验,,乙型肝炎病毒;,脱氧核糖核酸;,荧光定量聚合酶链反应;,血清标志物;,酶联免疫吸附试验,HBVDNA与H
【摘要】目的: 探讨荧光定量PCR检测HBV DNA与HBVm的关系。 方法: 采用荧光定量PCR法和酶联免疫吸附试验(ELISA)对159份HBVm 8种不同阳性模式及67份HBVm全阴模式血清进行HBV DNA检测。 结果: HBsAg、HBcAb、HBeAe阳性者HBV DNA阳性率为8983%; HBsAg、HBcAb、HBeAb阳性者HBV DNA阳性率为2881%; HBsAb、HBcAb、HBeAb阳性者HBV DNA阳性率为1666%; HBVm全阴性者HBV DNA阳性率为1791%。 结论: 荧光定量PCR法检测HBV DNA是乙型肝炎病毒复制最直接可信的指标,可反映HBV真实感染和复制状态,特别是低复制状态,明显优于ELISA法检测HBVm,具有重要临床意义。【关键词】乙型肝炎病毒; 脱氧核糖核酸; 荧光定量聚合酶链反应; 血清标志物; 酶联免疫吸附试验
Comparative Analysis between HBV DNA by FQPCR and HBVm by ELISA
LIU Jinlu, LI Caiqing, LU Cheng, et al
The First Affiliated Hospital, Hebei North University, Zhangjiakou, 075000, Hebei China
【ABSTRACT】Objective: To investigate the relationship between HBVDNA determined by the polymerase chain reaction (PCR) assay and HepatitisB markers by ELISA method.Methods: The serum samples from 159 cases with 8 different positive models and 67 cases with all negative models were tested by Fluorescence quantitative PCR assay (FQPCR) and also by ELISA to compare the results.Results: Among the patients,the positive rate of HBVDNA for the patients with positive HBsAg、HBcAB and HBeAe was 8983%;the positive rate of HBVDNA for the patients with positive HBsAg、HBcAb and HBsAb was 2881%;the positive rate of HBVDNA for the patients with positive HBsAb、HBcAb and HBeAb was 1666%;the positive rate of HBV DNA for the patients with all negative HBVm was 1791%.Conclusione: HBVDNA determined by PCR assay is much more corrct and sensitive than HBVmarkers by ELISA assay.FQPCR could be used as a excellent monitor for the state of HBV irfection and its complication, especially for the state of low complication. ......
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