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聚合酶链反应检测HBVM阳性血清中HBV DNA的临床意义
引用本文:孙燕,黄兴华.聚合酶链反应检测HBVM阳性血清中HBV DNA的临床意义[J].天津医药,1997,25(5):288-290.
作者姓名:孙燕  黄兴华
作者单位:江苏启东肝癌研究所 226200(孙燕,黄兴华),江苏启东肝癌研究所 226200(王能进)
摘    要:应用聚合链反应对140例乙型肝炎病毒感染标志(HBV M)阳性的慢性肼病患者血清中HBV DNA进行检测。结果发现:1.HBV DNA总阳性率为72.86%;BHsAg、HBeAg和抗HBc阳性血清中HBVDNA阳性纺分别为76.56%、96.15%和74.42%;HBsAg阴性血清中HBVDNA阳性率为33.33%,HBeAg阴性血清中HBVDNA阳性率为59.09%。2.各HBV感染模式中,H

关 键 词:聚合酶链反应  乙型肝炎病毒  DNA  诊断

Clinical Significance of HBV DNA Detection in HBV M-Positive Sera Using Polymerase Chain Reaction
Sun Yan,Huang Xinghua,Wang Nengjin Qidong Liver Cancer Institute,Jiangsu.Clinical Significance of HBV DNA Detection in HBV M-Positive Sera Using Polymerase Chain Reaction[J].Tianjin Medical Journal,1997,25(5):288-290.
Authors:Sun Yan  Huang Xinghua  Wang Nengjin Qidong Liver Cancer Institute  Jiangsu
Institution:Sun Yan,Huang Xinghua,Wang Nengjin Qidong Liver Cancer Institute,Jiangsu 226200
Abstract:HBV M-positive sera from 140 patients with chronic hepatosis had been searched for HBV DNA using polymerase chain reaction (PCR). The results showed that 72. 86% (102/140)of the samples were positive for HBV DNA ;the HBV DNA frequency in HBsAg-positive. HBeAg-positive or anti-HBc-positive sera were 76. 56%(98/128) ,96. 15% (50/52) ,and 74. 42%(96/129) respectively. Of 12 HBsAg-negative sera, 4 were positive for HBV DNA (33. 3%); of 88 HBeAg-negative. sera, 52 were positive for HBV DNA(59. 09%). Of all the eight HBV infection patterns,the one which was positive for HBsAg.HBeAg and anti-HBc had the highest HBV DNA positivity of 96. 15% (50/52), significantly higher than other patterns(P<0. 025-0. 001). The results suggested that the antigenic-ity of HBsAg was not correlated to infectiousness;HBeAg was an important marker showing activity and infectiousness of HBV;anti-HBc,as a HBV marker,had its clinical special significance in regions with higher hepatocarcinoma risk. It confirmed that PCR amplification was a valuable tool for diagnosing HBV infection states,especially for observing curative effect or recurrence of hepatitis.
Keywords:polymerase chain reaction (PCR) HBV marker(HBV M) HBV DNA
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