摘要
目的:研究聚合酶链反应(polymerase chain reaction,PCR)和反向斑点杂交(reverse dot blot,RDB)技术在人乳头瘤病毒(human papillomavirus,HPV)感染检测中的情况,进一步研究其应用价值。方法:收集2013年3月至2015年6月宫颈癌、尖锐湿疣、宫颈上皮内瘤变三种类型疾病共320例脱落细胞标本,采用PCR和RDB杂交技术对HPV基因型进行检测,分析检测数据。结果:在宫颈癌、尖锐湿疣、宫颈上皮内瘤变的感染中HPV单基因型感染均多于多重基因型感染,但不同疾病中单基因型感染患者比率差别不明显,分别为82.50%、84.06%、84.30%;不同疾病中多重基因型感染患者例数分别为17.50%、15.94%、15.70%,两种类型感染情况比较,差异无统计学意义(P>0.05);320例标本中检测出的210例阳性标本进行分型,反复检验后数据显示HPV16为最主要的感染基因型。结论:PCR和RDB技术是HPV基因型检测的有效方法,也是关于进行HPV感染防治的有效检测指标。
Objective:To study the value of polymerase chain reaction( PCR) and reverse dot blot( RDB) in the detection of human papillomavirus( HPV) infection. Methods:320 exfoliative cells samples of cervical cancer,condyloma acuminatum,and cervical intraepithelial neoplasia from March 2013 to June 2015 were collected and the HPV genotype was detected by PCR and RDB. Results:The HPV haplotype infection rates in cervical cancer,condyloma acuminatum,and cervical intraepithelial neoplasia were higher than the infection rates in multiple genotypes. The HPV haplotype infection rates were 82. 50 %,84. 06 % and 84. 30 % respectively and in multiple genotypes were 17. 50 %,15. 94 % and15. 70 % respectively. There was no significant difference of infection in each group( P〈0. 05). HPV16 was the most common infection genotype in the 210 positive samples after repeated detection. Conclusion:PCR and RDP are effective methods in the detection of HPV genotype as well as in HPV prevention and treatment.
出处
《包头医学院学报》
CAS
2017年第2期29-30,共2页
Journal of Baotou Medical College
关键词
基因分型
聚合酶链反应
反向斑点杂交技术
人类乳头瘤病毒
Genotyping
Polymerase chain reaction(PCR)
Reverse dot blotting(RDB)
Human papillomavirus(HPV)