乙肝HBeAg、前S1-抗原与HBV-DNA相关性研究  被引量:4

Correlation between HBE Ag, Pre-S1 antigen and HBV-DNA

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作  者:邵咏[1] 吕惠娟 邢志广[1] 

机构地区:[1]新乡医学院第二附属医院,河南新乡453002 [2]新乡市卫校,河南新乡453000

出  处:《现代预防医学》2015年第11期2069-2071,共3页Modern Preventive Medicine

摘  要:目的探讨乙肝HBe Ag、前S1-抗原和HBV-DNA的相关性,为临床诊疗提供实验室依据。方法乙肝HBe Ag和前S1-抗原检测采用ELISA法,HBVDNA载量采用PCR-荧光探针法。结果 (1)前S1-抗原阳性率HBe Ag(+)组91.25%(73/80)显著高于HBe Ag(-)组25.48%(40/157)(χ2=37.552,P〈0.005);HBVDNA阳性率HBe Ag(+)组88.75%(71/80)亦显著高于HBe Ag(-)组29.30%(46/157)(χ2=30.508,P〈0.05)。(2)HBe Ag阳性率HBV-DNA高水平复制组(即〉107拷贝/ml)82.22%(37/42)显著高于低水平复制组(即103~105拷贝/ml)45.0%(9/20)(χ2=10.78,P〈0.05);前S1-抗原阳性率HBV-DNA高水平复制(即〉107拷贝/ml)组96.15%(42/45)亦显著高于低水平复制(即103~105拷贝/ml)组45.0%(9/45)(χ2=30.508,P〈0.005)。结论乙肝HBe Ag、前S1-抗原与HBV-DNA检测,一致性较好,两者均可作为乙肝病毒复制和传染的实验室指标。Objective To explore the correlation between HBE Ag, Pre-S1 antigen, HBV-DNA, and provide basis for clinical diagnosis and treatment. Methods The detection of HBeAg and pre-S1 antigen were carried out by the ELISA method, and HBVDNA load was detected by the PCR- fluorescent probe method. Results Pre-S1 antigen positive rate of HBE Ag (+) group was significantly higher than that of the negative group (P〈0.005); HBV DNA positive rate of HBE Ag (+) group was significantly higher than that of HBE Ag (-) group (P〈0.05). The HBE Ag positive of HBV - high levels of DNA replication was significantly higher than that of low copy group (P〈O.05). Pre-S 1 antigen positive rate of HBV - high levels of DNA replication were significantly higher than that of the low level copy group. Conclusion The positive rates of HBE Ag, pre S1- antigen and HBV-DNA have high consistency, and all can be used as laboratory indicators of the HBV replication and infection.

关 键 词:HBE Ag 前S1-抗原 HBV-DNA载量 

分 类 号:R186[医药卫生—流行病学]

 

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