检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
机构地区:[1]中山大学附属第一医院检验医学部,广东广州510080
出 处:《分子诊断与治疗杂志》2009年第1期20-22,共3页Journal of Molecular Diagnostics and Therapy
摘 要:目的探讨乙型肝炎病毒前S1抗原(HBV PreS1-Ag)与HBV-DNA和HBV表面标志物(HBV-M)以及转氨酶之间的关系。方法从临床检测HBV-M的标本中筛出HBV阳性病例150例,采用ELISA法检测乙肝前S1抗原和荧光定量PCR法检测标本HBV-DNA,并与25例HBsAb(+)和5例HBV-M全阴性血清进行比较,同时采用酶法检测所有血清标本的天冬氨酸氨基转移酶(AST)和丙氨酸氨基转移酶(ALT)。结果HBV-DNA和HBV PreS1-Ag在HbeAg(+)组中检出率分别为100%和90.1%,在HbsAg(+)+HbeAb(+)+HbcAb(+)组中检出率为48.1%和40%。在HbsAg(+)+HbcAb(+)和单纯HbsAg(+)两组中,HBV-DNA与前S1抗原仍有一定检出率。HBV PreS1-Ag(+)组中,ALT与AST异常率分别占54.3%和46.7%。结论HBV-DNA检测为反映乙肝病毒复制最灵敏、特异的方法,乙肝前S1抗原检测成本低廉,与HBV-DNA的符合度较高,是对乙肝"两对半"和HBV-DNA测定的重要补充和加强,适合在没有条件开展HBV-DNA定量的广大基层医院推广。Objective To study the relationship between HBV PreS1-Ag、HBV-DNA、HBV-M and hepatic enzyme in patient infected with HBV. Methods The serum pre-S1 antigen and HBV-DNA were tested by ELISA and real-time fluorescent quantitative PCR(RT-PCR) in 150 patients infected with HBV screening HBV-M by ELISA method. At the mean time, 25 HBV-Ab(+) and 5 HBV-M negative samples were tested. Aspartate aminotransferase(AST) and alanine aminotransferase(ALT) were tested by rate method in all samples. Results The positive rates of the pre-S1 antigen and HBV-DNA were highest in HbeAg’s positive patients with different serology models of hepatitis B virus infection, which were 90.1% and 100% separately. The positive detection rates for pre-S1 antigen and HBV-DNA in the HbsAg(+)+HbeAb(+)+HbcAb(+) model were 40.2% and 48.1% separately. There still had a little positive rate of HBV-DNA and Pre S1-Ag in the HbsAg (+)+HbcAg(+) model and HbsAg(+) model. The abnormal rate of ALT and AST in the pre-S1 antigen’s positive model were higher than that in pre-S1 antigen’s negative model (ALT 54.3% and 0, AST 46.7% and 0). Conclusion The detection of HBV-DNA is the most sensitive and specific method reflecting the replication of hepatitis B virus in clinical. Hepatitis B virus Pre S1-Ag detection can be used as a supplement to hepatitis B markers and HBV-DNA detection. Especially hepatitis B virus Pre S1-Ag detection is suitable to widely been applied in grass-roots hospital lack of condition for real-time fluorescent quantitative PCR.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.69