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作 者:李珉珉[1] 洪丹妮[1] 朱勤爱[1] 朱穗兰[1]
机构地区:[1]暨南大学附属第一医院临床检验中心,广东广州510630
出 处:《暨南大学学报(自然科学与医学版)》2011年第6期637-640,共4页Journal of Jinan University(Natural Science & Medicine Edition)
基 金:广东省医学科研基金项目(A2010327)
摘 要:目的:联合检测慢性乙型肝炎病毒(HBV)携带者的血清前S1(PreS1)抗原和乙肝e抗原(HBeAg)两项指标,判断其与HBV-DNA定量的相互关系。方法:采用双抗体夹心酶联免疫吸附分析(ELISA)法(两步法)检测PreS1抗原,双抗体夹心ELISA法(一步法)检测HBeAg,实时荧光定量聚合酶链反应(PCR)法检测HBV-DNA。结果:在335例慢性HBV携带者患者中,PreS1抗原阳性率为42.7%,HBeAg阳性率为36.4%,HBV-DNA阳性率为53.4%。在179例HBV-DNA阳性患者中,HBeAg阳性109例(60.9%);156例HBV-DNA阴性患者中,HBeAg阴性143例(91.7%)。在179例HBV-DNA阳性患者中,PreS1抗原阳性89例(49.7%);在156例HBV-DNA阴性患者中,PreS1抗原阴性102例(65.4%)。PreS1和HBeAg双阳性的感染者HBV-DNA阳性率为93.8%(45/48);在PreS1和HBeAg双阴性的感染者中,HBV-DNA阳性率仅为22.0%(26/118)。结论:HBeAg与HBV-DNA的相关性比PreS1抗原与HBV-DNA的相关性高。PreS1和HBeAg双阳性的感染者HBV的复制程度高,而双阴性的感染者复制程度较低。因此,PreS1抗原与HBeAg联合检测可用于预测HBV-DNA的水平。Aim:To study the relationship of HBV-DNA with the HBV biomarkers PreS1 and HBeAgin chronic HBV-carriers. Methods: PreS1 and HBeAg were detected by sandwich ELISA. HBV-DNAwas detected by fluorescence quantitative polymerase chain reaction assay. Results: Among 335 chronicHBV-carriers'serum samples,the positivety rate of preS1, HBeAg and HBV-DNA were 42.7%, 36. 4%and 53.4%, respectively. Meanwhile, the positivety rates of preS1 and HBeAg in patients with serumHBV-DNA positive were 49.7% (89/179) and 60. 9% (109/179), respectively. The negative rates ofpreS1 and HBeAg in patients with serum HBV-DNA negative were 65.4% (102/156) and 91.7%(143/156), respectively. The positive rates of serum HBV-DNA in patients with PreS1 and HBeAg bothpositive were 93.8% (45/48), while only 22.0% (26/118) in patients with PreS1 and HBeAg bothnegative. Conclusion:There is a high correlation between HBeAg and HBV-DNA, indicating that HBeAghas a better concordance with HBV-DNA than PreS1. HBV carriers with PreS1 and HBeAg both posi-tivety have high HBV-DNA copies. The co-detection of PreS1 and HBeAg can predict the replication lev-el of HBV.
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