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作 者:朱子犁[1] 古丽巴哈尔 刘建军[1] 阳帆[1] 汪洪富[1] 张海龙[1] 何建凡[1]
机构地区:[1]深圳市疾病预防控制中心,广东深圳518020 [2]新疆哈密地区卫生防疫站,新疆哈密839000
出 处:《中国热带医学》2006年第7期1138-1139,共2页China Tropical Medicine
摘 要:目的研究乙肝血清学标志物(HBV-M)结果与HBV-DNA水平的关系,分析HBV DNA阳性率在各年龄组的分布情况。方法对深圳市部分服务行业人员血清应用荧光定量PCR检测和ELISA法检测并对结果进行分析。结果1 781例乙肝血清学标志物阳性血清中有1 102例HBV-DNA阳性。其中883例1.3.5阳性(俗称“大三阳”)血清中HBV-DNA的阳性率为96.15%;722例1.4.5阳性(俗称“小三阳”)血清中HBV-DNA的阳性率为24.38%;138例1.5阳性血清中HBV-DNA的阳性率为38.41%;22例1.3阳性血清中HBV-DNA的阳性率为90.91%;11例HBsAg阳性血清中HBV-DNA阳性率为36.36%。结论两种方法检测乙肝标志物有密切的相关性。荧光定量PCR是检测HBV-DNA含量较精确的方法,能正确反映乙肝病毒的复制水平和活跃程度;HBsAg和HBeAg与HBV-DNA含量有着明显的相关关系。Objective To analyze the relationship between the level of HBV DNA and the HBV - M. Methods Serum samples from 1 781 serviee workers were deteeted by ELISA and divided into nine groups: HBsAg( + )/HBeAg( + )/HBeAb( + ), HBsAg( + )/HBeAb( + )/HBeAb( + ), HBsAg( + )/HBeAb( + ), HBsAg( + )/HBeAg( + ), HBsAb/HBeAb( + ), HBeAb( + )/ HBeAb( + ), HBsAg( + )/HBeAb( + ), HBsAb( + ) and HBsAg( + ). HBV DNA eoneentration was determined by fluorescent quantitative PCR. Results The positive rate of HBV - DNA in the group of HBsAg( + )/HBeAg( + )/HBeAb( + ) was 61.88% (1 102/1 781), the positive rate in the group of HBsAg( + )/HBeAb( + )/HBeAb( + ) was 96.15% , the positive rate in the group of HBsAg( + )/HBeAb( + )/HBeAb( + ) was 24.38%, the positive rate in the group of HBsAg( + )/HBeAb( + ) was 38. 41%, 90.91% in. the group of HBsAg( + )/HBeAg( + ), 36.36% in the group of HBeAg( + ) and the positive rate of HBV - DNA was 0 % in the other groups. There signifieant differenees between the different hepatitis B sera positive modes and the result of HBV DNA. The HBV DNA level showed an obvious correlation with the HBeAg eontent in scra. Conclusion A elose eorrelation exists between these two methods in the detection of HBV markers. The FQ - PCR is a relatively aeurate method for detection of HBV - DNA.
关 键 词:乙肝病毒 HBV-DNA ELISA 荧光定量PCR 相关性
分 类 号:R373.2[医药卫生—病原生物学]
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