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作 者:李彩东[1] 吴斌[1] 段正军[1] 田鹏飞[1]
出 处:《国际检验医学杂志》2013年第B12期10-12,共3页International Journal of Laboratory Medicine
摘 要:目的探讨乙型肝炎病毒表面大蛋白(HBV-LP)用于临床诊断的价值以及与HBVDNA和丙氨酸氨基转移酶(ALT)的相关性,并分析其在不同性另4、年龄群体中的差异性。方法分.蓦4采用酶联免疫吸附试验(ELISA)、实时荧光定量PCR(RT—PCR)、化学发光法(CLIA)和全自动生化分析仪对1036例兰州地区慢性乙型肝炎病毒感染者血清中HBv.LP、HBVDNA、HBeAg以及ALT进行检测,并且分析比较三者之间的阳性率及相关性。结果HBeAg(+)模式的HBv-DNA与HBV—LP阳性率比较差异无统计学意义(P〉0.05),不受性别、年龄的影响。HBeAg(-)模式的HBV—DNA与HBv-LP阳性率比较差异有统计学意义(P〈0.05),男性组HBV-DNA阳性率略高于女性组,年长组大于年轻组,年轻群体HBV-LP阳性率略高于年长群体。HBeAg(+)模式群体中ALT〉50U/L的比例远大于HBeAg(-)模式群体。结论在HBeAg(+)模式群体中HBV—LP与HBV-DNA检测有较高符合性,HBeAg(+)模式群体中及年长群体中肝受损程度较明显,在HBeAg(-)模式群体中乙肝病毒大蛋白阳性率高于HBV-DNA。HBV-LP是反映HBeAg(-)乙肝病毒携带者病毒复制情况的血清免疫学指标,同时检测HBV—LP与HBV-DNA会更具有指导意义。Objective To study the value of the hepatitis B virus large suriace protein(HBV-LP) in chmcal diagnosis and its as- sociation with the level of HBV-DNA and ALT,to analyze their difference in gender and age groups. Methods Sera of 1 036 HBV carriers were collected. HBV-DNA level was qualitatively detected by using real-time polymerase chain reaction, HBV-LP was measured by enzyme linked immunosorbent assay(ELISA) and ALT was determined by fully-automatic biochemical analyzer in 1 036 cases of infected serum. Results There was no significant difference between the levels of HBV-DNA and HBV-LP(P^0.05) in HBeAg-positive patients,which was not affected by gender and age. Significant difference of positive rate was observed between HBV-DNA and HBV-LP in HBeAg-negative patients(P〈0.05). The positive rate of HBV-DNA in males was higher than that of females,in older group which was higher than that of younger. The rate of ALT〉50 U/L in HBeAg-positive patients were higher than that of HBeAg-negative ones. Conclusion There was higher coincidence rate between the levels of HBV-LP and HBV-DNA in HBeAg positive patients. The positive rate of HBV-LP was higher than that of HBV-DNA in HBeAg-negative patients and the liver function of HBeAg-positive patients and the older patients were significantly impaired. HBV-LP is a reliable serological marker which can reflect the replication of HBV in HBeAg-negative patients, Simultaneous detection of HBV-LP and HBV-DNA will be more useful.
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