Xia F, Xu Y H, Zheng M J, Wang X L
Department of Parasitology, Anhui Medical University, Hefei 230032, China.
Zhonghua Yu Fang Yi Xue Za Zhi. 2017 Jun 6;51(6):501-505. doi: 10.3760/cma.j.issn.0253-9624.2017.06.009.
To investigate the comparative study of serum hepatitis B virus (HBV) large protein (HBV-LP) , HBV-DNA, and Pre S1 antigen (Pre S1-Ag) detection in the evaluation of serum HBV replication in patients with chronic hepatitis B. A total of 482 patients infected with chronic hepatitis B virus (CHB) were enrolled and the serums were collected in a hospital of Hefei city in Anhui province from June 2013 to March 2015. The serum HBV-LP, HBV markers(HBV-M) and Pre S1-Ag were detected using ELISA, and HBV-DNA were quantified using quantitative real-time PCR. The positive detection rate difference of HBV-DNA, HBV-LP and Pre S1-Ag were compared, the correlation between the logarithm of HBV-DNA copies number and the absorbance value of HBV-LP was analyzed using Spearman rank correlation. The positive rates of HBV DNA, HBV-LP, and Pre S1-Ag were 67.22% (324/482), 73.86% (356/482), and 37.34% (180/482), respectively (0.01). The positive rates of the three markers were 54.57% (185/339), 64.90% (220/339), and 27.73% (94/339), respectively, in 339 HBeAg-negative CHB patients (0.01). In HBeAg negative patients, the positive rate of HBV-LP in 185 cases of HBV-DNA positive samples was 90.81% (168/185), which was higher than that of Pre S1-Ag with rate of 39.46% (73/185) (0.01).The positive rate of HBV-LP was 33.77% (52/154) in 154 cases of patients with negative HBV-DNA whose positive rate was higher than Pre S1-Ag with positive rate of 13.64% (21/154)(0.01). The positive rates of HBV-DNA, HBV-LP and Pre S1-Ag in HBsAg, HBeAg and HBcAb positive groups were 97.04% (131/135), 94.81% (128/135), and 60.00% (81/135), (0.01); The positive rates of three indexes of HBsAg, HBeAb, HBcAb positive group were 53.74% (122/227), 63.88% (145/227), and 27.31% (62/227); The positive rates of three indexes of HBsAg and HBcAb positive group were 55.79% (53/95), 67.37% (64/95), and 28.42% (27/95) (0.01). The absorbance value of HBV-LP was positively related with the logarithm of HBV-DNA copies number (Spearman rank correlation coefficient was 0.908, 0.01). There was a good correlation between HBV-LP and HBV-DNA load value, and could be used as an effective complement for the detection of HBV-DNA and HBV-M. Compared with Pre S1-Ag.
探讨血清乙肝病毒(HBV)大蛋白(HBV-LP)、HBV-DNA及前S1抗原(Pre S1-Ag)检测在评估慢性乙型肝炎患者血清HBV复制中的对比研究。选取2013年6月至2015年3月在安徽省合肥市某医院收治的482例慢性乙型肝炎病毒(CHB)感染患者,采集其血清。采用酶联免疫吸附测定法(ELISA)检测血清HBV-LP、乙肝病毒标志物(HBV-M)及Pre S1-Ag,采用定量实时荧光聚合酶链反应(PCR)对HBV-DNA进行定量检测。比较HBV-DNA、HBV-LP及Pre S1-Ag的阳性检出率差异,采用Spearman等级相关分析HBV-DNA拷贝数对数与HBV-LP吸光度值之间的相关性。HBV DNA、HBV-LP及Pre S1-Ag的阳性率分别为67.22%(324/482)、73.86%(356/482)及37.34%(180/482)(P<0.01)。339例HBeAg阴性CHB患者中,三种标志物的阳性率分别为54.57%(185/339)、64.90%(220/339)及27.73%(94/339)(P<0.01)。在HBeAg阴性患者中,185例HBV-DNA阳性样本中HBV-LP的阳性率为90.81%(168/185),高于Pre S1-Ag的阳性率39.46%(73/185)(P<0.01)。154例HBV-DNA阴性患者中HBV-LP的阳性率为33.77%(52/154),高于Pre S1-Ag的阳性率13.64%(21/154)(P<0.01)。HBsAg、HBeAg及HBcAb阳性组中HBV-DNA、HBV-LP及Pre S1-Ag的阳性率分别为97.04%(131/135)、94.81%(128/135)及60.00%(81/135)(P<0.01);HBsAg、HBeAb及HBcAb阳性组三项指标的阳性率分别为53.