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前S1蛋白与病毒DNA和核心抗原对乙型肝炎病毒复制诊断的对比
引用本文:李琴,孙桂珍,魏玉香,闵福援,丛玉隆,欧晓娟,王宝恩.前S1蛋白与病毒DNA和核心抗原对乙型肝炎病毒复制诊断的对比[J].中华肝脏病杂志,2004,12(3):134-136.
作者姓名:李琴  孙桂珍  魏玉香  闵福援  丛玉隆  欧晓娟  王宝恩
作者单位:1. 100050,北京,首都医科大学附属北京友谊医院肝病研究中心
2. 北京佑安医院临床检验科
3. 北京解放军总医院临床检验科
基金项目:北京市科技计划项目(H020920020091)
摘    要:目的 分析前S1(Pre-S1)蛋白在诊断慢性乙型病毒性肝炎病毒复制中的作用。 方法 收集慢性乙型病毒性肝炎患者共104例,均经肝活组织检查证实。检测其Pre S1蛋白,HBV标志物与HBV DNA。结果 HBsAg、HBeAg、抗-HBc阳性者29例,HBV DNA与Pre-S1蛋白的检出率均达96.5%,这组患者存在病毒的高复制。HBsAg、抗-HBe和抗-HBc阳性者65例,HBV DNA与Pre-S1蛋白的检出率分别为81.5%和72.3%;HBsAg和抗-HBc阳性者8例,HBV DNA与Pre-S1蛋白的检出率分别为87.5%、75.0%,说明部分HBeAg阴性而抗-HBe阳性/阴性的患者仍存在着病毒复制。以HBV DNA定量>103拷贝/ml为诊断标准,HBV DNA阳性患者HBeAg、Pre-S1蛋白的检出率分别为31.5%(28/89)、80.9%(72/89);两者与HBV DNA的总符合率分别为40.0%(42/104)、82.0%(85/104)。HBV DNA与HBeAg检出率差异有显著性(x2=53.397,P<0.001);HBV DNA与Pre-S1蛋白检出率差异无显著性。 结论Pre-S1蛋白较HBeAg更敏感的反映了HBV复制的情况。

关 键 词:前S1蛋白  病毒DNA  核心抗原  乙型肝炎病毒  病毒复制  诊断  检测
修稿时间:2003年7月1日

The contrast study of Pre-S1 protein, HBV-DNA and HBeAg in diagnosing viral replication in patients with chronic hepatitis B
LI Qin,SUN Gui-zhen,WEI Yu-xiang,MN Yu-yuan,CONG Yu-long,OU Xiao-juan,WANG Bao-en. Liver Research Center,Beijing Friendship Hospital Affiliate of Capital University of Medical Sciences,Beijing ,China Corresponding author: LIN Qin..The contrast study of Pre-S1 protein, HBV-DNA and HBeAg in diagnosing viral replication in patients with chronic hepatitis B[J].Chinese Journal of Hepatology,2004,12(3):134-136.
Authors:LI Qin  SUN Gui-zhen  WEI Yu-xiang  MN Yu-yuan  CONG Yu-long  OU Xiao-juan  WANG Bao-en Liver Research Center  Beijing Friendship Hospital Affiliate of Capital University of Medical Sciences  Beijing  China Corresponding author: LIN Qin
Institution:Liver Research Center, Beijing Friendship Hospital Affiliate of Capital University of Medical Sciences, Beijing 100050, China.
Abstract:Objective To determine the role of Pre-S1 protein in diagnosing viral replication in patients with chronic hepatitis B. Methods 104 consecutive patients with chronic hepatitis B were included in the study, liver biopsy were performed in all patients. Serial serum samples were studied with the quantitative determination of HBV-DNA by a quantitative PCR assay, determination of Pre-Sl protein by ELISA. Results The positive rates of HBV-DNA and Pre-Sl protein in patients with HBsAg HBeAg anti-HBc( ) both were 96.5%. The positive rates of HBV-DNA and Pre-Sl protein in patients with HBsAg anti-HBe anti-HBc( ) were 81.5%, 72.3%, respectively. The positive rates of HBV-DNA and Pre-Sl protein in patients with HBsAg anti-HBc( ) were 87.5%,75.0%, respectively. It represented some patients with HBeAg (-) anti-HBe ( /-) still had viral replication. HBV-DNA>103 copy/ml as positive criteria for diagnosing viral replication, the positive rate of HBeAg, Pre-Sl were 31.5%(28/89), 80.9% (72/89) in patients with HBV-DNA>103 copy/ml, respectively. The concordance rates of HBeAg, Pre-Sl with HBV-DNA were 40.0% (42/104), 82.0%(85/104), respectively. Conclusion It showed that Pre-S 1 was more sensitive than HBeAg in diagnosing viral replication in patients with chronic hepatitis B.
Keywords:Pre-S1 protein  Hepatitis B virus  Hepatitis B e antigen  Viral replication
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