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机构地区:[1]山东省临沂市沂水中心医院,山东临沂276400
出 处:《医学检验与临床》2013年第4期10-11,共2页Medical Laboratory Science and Clinics
摘 要:目的:以DNA测序法为标准,探讨不对称PCR熔解曲线法检测乙型肝炎病毒A1762T/G1764A基因变异的敏感性和特异性。方法:选取45例HBV阳性且经PCR熔解曲线法显示A1762T/G1764A变异的乙型肝炎患者血清,另选10例未发生HBV A1762T/G1764A变异的慢乙肝患者血清,用DNA测序法进行比较,分析两者检测结果。结果:55例测序样本中有51例两法结果完全一致,总符合率92.7%,另4例结果是:不对称PCR熔解曲线法检测显示为不完全变异型,而测序法则显示为完全变异型。结论:两法的相符率高,PCR熔解曲线法对A1762T/G1764A变异的检测是一简单易行较实用的方法,适用于临床基层开展。Objective:Taking DNA sequencing methods as the standard, to explore the sensitivity and and specificity of A1762T/G1764A mutation by PCR melting curve method. Methods:Choose 45 samples that the serumA1762T/G1764A mutation of patients were detected by PCR melting curve method, there patients HBV-DNA. Moreover choose other 10 samples that have not had the A1762T/G1764A variation. All detected by DNA sequencing method. Analysis results in different methods.Results:In the 55 samples, there are 51 samples whose result sare consistent, the total coincidence rate is 92.7%.Conclusions:The coincidence rate of two methods is high. It means that using PCR melting curve method to detect A1762T/G1764A variation is an easy and feasible practical method, and is suitable used in clinical and the basic units.
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