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作 者:汪东剑[1] 张晓云[1] 刘冬萍[1] 冯丽霞[1] 邱华琴[1] 徐波[1]
机构地区:[1]中国人民解放军第一八四医院输血科,鹰潭335000
出 处:《中华微生物学和免疫学杂志》2014年第12期950-953,共4页Chinese Journal of Microbiology and Immunology
摘 要:目的:探讨PCR-反向点杂交基因分型检测阳性率与病毒核酸载量间的关系。方法采用PCR荧光法对1162例女性患者进行HR-HPV DNA载量检测,采用PCR-反向点杂交法对其中141例高危HR-HPV DNA阳性标本进行HPV基因分型检测。结果基因分型检测总阳性率为68.8%,基因分型检测阳性率与HR-HPV DNA载量对数值呈显著正相关(r=0.944,P﹤0.01),其二次项曲线拟合公式为Y=-1.806+0.558X-0.031X2(Y为基因分型阳性率,X为HR-HPV DNA载量对数值)。不同载量组间的基因分型检测阳性率差异具有统计学意义(P﹤0.01):当HR-HPV DNA载量在10^4~10^5拷贝/ml、10^5~10^6拷贝/ml、10^6~10^7拷贝/ml和>10^7拷贝/ml时,使用不同厂家基因分型检测试剂其阳性率分别为27.8%、48.5%、74.0%、97.5%和33.3%、51.5%、78.0%、97.5%。结论PCR-反向点杂交法基因分型检测阳性率与其核酸载量相关。Objective To investigate the correlation between the positive rate of PCR-reverse dot blot genotyping test and the loads of the viral nucleic acid. Methods The fluorescent PCR assay was used to detect the high-risk HPV(HR-HPV)DNA loads in the cervical mucus samples from 1162 female patients. Patients with positive HR-HPV DNA were further analyzed by PCR-reverse dot blot hybridization assay for HPV genotyping. Results The overall positive rate of genotyping test was 68. 8% . The positive rate of genotyping test had a significant positive correlation with the Log Koc of HR-HPV DNA loads(r=0. 944, P﹤0. 01). The quadratic curve fitting formula was Y= -1. 806+0. 558X-0. 031X2(Y for genotyping positive rate,X for Log Koc of HR-HPV DNA loads). There were significant differences with the positive rate of genotyping test among patients with different viral loads(P﹤0. 01). When HR-HPV DNA loads were 10^4-10^5 copies/ ml,10^5-10^6 copies/ ml,10^6-10^7 copies/ ml and more than 10^7 copies/ ml,the positive rate of HPV genotyping test were 27. 8% ,48. 5% ,74. 0% ,97. 5% and 33. 3% ,51. 5% ,78. 0% ,97. 5% respectively by using different genotyping detection reagents. Conclusion The positive rate of PCR-reverse dot blot genotyping test was correlated with the loads of HPV nucleic acid.
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