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作 者:刘键[1] 蒋英[2] 吴正林[1] 黄烈[1] 庄鹏[1]
机构地区:[1]深圳市第四人民医院检验医学部,广东深圳518033 [2]深圳市福田区慢性病防治院检验科
出 处:《实用预防医学》2014年第5期607-609,共3页Practical Preventive Medicine
基 金:深圳市福田区公益性科研项目深圳市科技局项目(编号FTWS081)
摘 要:目的探讨乙型肝炎病毒表面大蛋白(LHBs)检测对乙型肝炎诊断的实验价值。方法采用酶联免疫吸附实验(ELISA)和荧光定量PCR法对1 049例HBsAg阳性及694例HBeAg阴性慢性乙肝患者血清标本进行HBV DNA和LHBs检测。结果 HBsAg阳性患者中HBV DNA阳性率为66.12%(653/1 049),LHBs阳性率为68.18%(677/1 049),二者差异无统计学意义(χ2=1.18,P>0.05);LHBs含量与HBV DNA拷贝数对数值呈正相关性;HBeAg阴性慢性乙肝患者中HBV DNA与LHBs检出阳性率分别为43.80%(304/694)和51.73%(359/694),二者差异有统计学意义(χ2=8.74,P<0.01)。结论 LHBs能反映乙型肝炎病毒复制情况;对HBeAg阴性慢性乙肝患者而言,LHBs更能反映体内HBV感染和复制状态。Objective To explore the experimental value of hepatitis B virus large surface protein (LHBs) in the diagnosis of hepatitis B. Methods Enzyme- linked immunosorbent assay (ELISA) and fluorescence- based quantitative PCR were used for detection of HBV DNA and LHBs in 1,049 HBsAg - tx)sitive and 694 HBeAg - negative patients with chronic hepatitis B. Results The positive rates of HBV DNA and LHBs in HtKsAg- positive patients were 66.12 % (653/1,049) and 68.18 % (677/1,049) respectively, and no statistically significant difference was found between them (X^2-1.18, P 〉 0.05 ). The serum LHIKs concentration was positiwe correlated with the logarithmic value of HBV DNA copies among 653 HBV DNA positive pa- tients. The positive rates of HI3V DNA and LHBs in HBeAg negative patients were 43.80 % (304/694) and 51.73 % (359/ 694) respectively, with statistically significant differences (X^2 -8.74, P〈 0.01). Conclusions LHtKs can reflect the repli- cation of HBV. Compared with HBV DNA, LHI3s is a better biological marker to reflect the infection and duplication of HBV among HBeAg- negative chronic hepatitis t3 patients.
关 键 词:乙型肝炎 乙型肝炎病毒外膜大蛋白 HBV DNA
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