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机构地区:[1]淮南市第一人民医院检验科,安徽省淮南232007
出 处:《中国基层医药》2010年第14期1877-1878,共2页Chinese Journal of Primary Medicine and Pharmacy
摘 要:目的探讨慢性HBV感染者血清HBVDNA载量与HBeAg/抗-HBe以及丙氨酸转氨酶(ALT)水平之间的关系。方法采用酶联免疫吸附法(ELISA)检测134例慢性HBV感染者HBV血清标志物,根据HBeAg/抗-HBe检测结果将患者分为Ⅰ组(HBeAg+/抗-HBe-,43例);11组(HBeAg-/抗-HBe+,69例);Ⅲ组(HBeAg-/抗-Hbe-,22例)。同时应用实时荧光定量PCR方法以及连续监测法检HBVDNA载量以及ALT水平。结果Ⅰ组HBVDNA阳性率和HBVDNA载量明显高于Ⅱ、Ⅲ组(P〈0.01)。HBVDNA阳性患者ALT异常率高于HBVDNA阴性患者(P〈0.01)。HBVDNA阳性患者HBVDNA载量与ALT水平之间无相关性(r=0.174,P=0.156)。结论血清HBVDNA载量与HBeAg/抗-HBe以及ALT之间存在一定的关系,但不能单纯依靠HBeAg/抗-HBe以及ALT来判断HBV在体内的复制情况,三项指标联合检测对HBV慢性感染者的病情检测、治疗具有重要意义。Objective To explore the relationship among HBV DNA load, HBeAg/Anti-HBe and ALT in patients with chronic hepatitis B infection. Methods HBV markers in 134 patients with chronic HBV infection were detected by FLISA, and patients were divided into group (HBeAg +/Anti-HBe-,43 patients) , group Ⅱ (HBeAg-/Anti- HBe + ,69 patients) and group Ⅲ( HBeAg-/Anti-Hbe-,22 patients) according to the results of presence of HBeAg/ Anti-IIBe. HBV DNA load and ALT were tested respectively by fluorescence quantitative polymerase chain reaction successive monitor reaction. Results Both the positive rate and the HBV DNA load quantification in group Ⅰ were higher than in group Ⅱ and Ⅲ( P 〈 0. 01 ). Abnormality rate of ALT in HBV DNA positive patients was higher than the patients with HBV DNA negitive( P 〈 0.01 ). There was no relationship between HBV DNA load and ALT in HBV DNA positive patients. Conclusion There was a certain corelation among HBV DNA load, HBeAg/An-ti-HBe and ALT,but the active degree of HBV replication could not to be assessed by HBeAg/Anti-HBe or ALT alone. It was necessary for the padient with chronic HBV infection to examine them together.
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