INTERMETHOD VARIATION IN DETECTION OF HUMAN PAPILLOMAVIRUS DNA IN CERVICAL SMEARS

Citation
Hl. Smits et al., INTERMETHOD VARIATION IN DETECTION OF HUMAN PAPILLOMAVIRUS DNA IN CERVICAL SMEARS, Journal of clinical microbiology, 33(10), 1995, pp. 2631-2636
Citations number
20
Categorie Soggetti
Microbiology
ISSN journal
00951137
Volume
33
Issue
10
Year of publication
1995
Pages
2631 - 2636
Database
ISI
SICI code
0095-1137(1995)33:10<2631:IVIDOH>2.0.ZU;2-M
Abstract
In order to investigate the reliability of detection of human papillom avirus (HPV) DNA in cervical smears, we have compared the performance of two HPV PCR systems, the CPI/IIG and MY09/11 primer-mediated PCRs a nd the Hybrid Capture System HPV DNA detection test (hybrid capture as say), in detecting HPV DNA in cervical smears. We also included in our study the MY09/11B PCR plus SHARP (solution hybridization assay for P CR products) Signal System, This SHARP Signal System was recently deve loped to detect RaY09/ 11B-generated biotinylated PCR products, The de tection rate of the hybrid capture assay was lower than those of the C PI/IIG and MY09/11 PCRs and the MY09/11B PCR plus SHARP Signal System. The detection rates of the CPI/IIG PCR and the MY09/11B PCR plus SHAR P Signal System were similar and higher than that of the conventional MY09/11 PCR system. The agreement beyond chance of the PCR methods was nearly perfect (kappa value between 0.82 and 0.84). The agreement bey ond chance of the hybrid capture assay and the PCR methods was fair to good (kappa value between 0.64 and 0.70). The systems detected HPV DN A in different hut overlapping sets of smears, Our results indicate th at each of the detection methods alone underestimates the prevalence o f HPV.