Correlation analysis of positive rate of HPV genotyping test and HPV nucleic acid loads
10.3760/cma.j.issn.0254-5101.2014.12.010
- VernacularTitle:人乳头瘤病毒基因分型检测阳性率与其核酸载量的相关性研究
- Author:
Dongjian WANG
;
Xiaoyun ZHANG
;
Dongping LIU
;
Lixia FENG
;
Huaqin QIU
;
Bo XU
- Publication Type:Journal Article
- Keywords:
Human papillomavirus;
Viral load;
Polymerase chain reaction;
Genotyping;
Reverse dot blot
- From:
Chinese Journal of Microbiology and Immunology
2014;(12):950-953
- CountryChina
- Language:Chinese
-
Abstract:
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 pa-tients. Patients with positive HR-HPV DNA were further analyzed by PCR-reverse dot blot hybridization as-say 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 gen-otyping test among patients with different viral loads(P﹤0. 01). When HR-HPV DNA loads were 104-105 copies/ ml,105-106 copies/ ml,106-107 copies/ ml and more than 107 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% respective-ly 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.
