摘要
目的探讨乙型肝炎(乙肝)病毒DNA的拷贝数(HBV DNA)与HBeAg、抗-HBe的相关性。方法对883例乙肝患者采用美国雅培公司AXSYM全自动酶免疫分析仪及配套试剂,进行微粒子酶免分析(MEIA)法检测HBeAg、抗-HBe和Roche COBAS AMPLICOR定量PCR仪及COBAS AMPLICOR HBV MONITORTM试剂盒内标法检测患者的HBV DNA,并进行相关性分析。结果(1)HBV DNA与HBeAg呈线性正相关(r=0．505,P<0．01 Mean:HBV DNA:7．12×1012拷贝／ml; HBehg:218．31 S／CO)。DNA含量104拷贝／ml对应HBeAg:104 S／CO;DNA含量在105-108拷贝／ml,HBeAg:112 S／CO;DNA含量109-1015拷贝／ml,HBeAg:252S／CO。(2)HBV DNA与抗-HBe无线性正相关(r=-0．052,P=0．477>0．05 Mean:HBV DNA 8．0×1010拷贝／ml,抗-HBe:0．18 S／CO)。结论HBV DNA与HBeAg呈线性正相关,HBeAg>100 S／CO,HBV DNA>104拷贝／ml,病毒复制活跃。HBV DNA与抗-HBe无线性正相关性,HBeAg阴性、抗-HBe阳性,病毒复制有所下降,但病毒载量仍较高,不可忽略其传染性。
Objective To better understand the duplication of hepatitis B virus （HBV） in order to improve clinical diagnoses and treatments via quantitative measurement of HBV-DNA and comparison of correlation of HBV-DNA with HBeAg and anti-HBe. Methods For 883 hepatitis B patients with positive HBsAg, HBV-DNA was measured by COBAS AMPLICOR HBV MONITOR^TM reagent and COBAS AMPLICOR quantitative PCR instrument. Microparticle enzyme immunoassay analysis （MEIA） was then carried out with fully automatic enzyme immunoassay analysis instrument made by Abbott Axsym from the U.S. to measure HBeAg and anti-HBe. Correlation was analysed by SPSS. Results （1）Positive correlation between 690 HBV-DNA positive and HBeAg positive with r = 0. 505 （P〈 0.01 ） was found with mean values as：HBV-DNA：7.12 × 10^12 copies/ml;HBeAg：218.31 S/CO. HBV-DNA： 10^4 copies/ml, HBeAg： 104 S/CO; HBV-DNA： 10^5-10^8 copies/ml, HBeAg： 112 S/CO; HBV-DNA： 10^9-10^15 copies/ml, HBeAg： 252 S/CO. （2） No correlation was found between 193 HBV-DNA and anti-HBe ＋ with r= 0.052（P= 0.477〉0.05） with Mean：HBV-DNA：8.0×10^10 copies/ml anti-HBe：0.18 S/CO. Conclusion HBV-DNA and HBeAg appeared to have had linear correlation, showing that HBeAg〉 100 S/CO,HBV-DNA〉 10^4 copies/ml and hepatitis B virus were reproduced. However,HBV-DNA did not show linear correlation with anti-HBe as HBeAg negative and anti-HBe positive, the level of hepatitis B viral replication decrease slightly. But the virus load is still high. Infectivity can not neglect.
出处
《中华流行病学杂志》
CAS
CSCD
北大核心
2006年第8期709-711,共3页
Chinese Journal of Epidemiology
