PMID- 24648936 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20211021 IS - 2049-9434 (Print) IS - 2049-9442 (Electronic) IS - 2049-9434 (Linking) VI - 1 IP - 2 DP - 2013 Mar TI - Evaluation of a novel real-time fluorescent polymerase chain reaction assay for high-risk human papilloma virus DNA genotypes in cytological cervical screening. PG - 280-284 AB - It has been confirmed that detection of high-risk human papillomavirus (HR HPV) DNA is useful in cervical cancer (CC) screening. Recently, a new real-time fluorescent polymerase chain reaction (PCR) assay was developed to detect HR HPV. This assay can synchronize nucleic acid amplification and testing using specific primers for 13 types of HR HPV genomes, combined with specific TaqMan fluorescent marker probe techniques through the fluorescence automatic PCR instrument. Furthermore, it uses TaqGold DNA polymerase, which minimizes the amount of non-specific amplification and increases the sensitivity of the assay. The aim of this study was to evaluate the analytical and clinical performance of the real-time fluorescent PCR assay in CC screening, compared to the Qiagen Hybrid Capture((R)) II High-Risk HPV DNA test((R)) (HC II). In total, 1,252 cervical specimens were collected from women between 19 and 71 years of age. The specimens were examined with three different assays, real-time fluorescent PCR assay and HC II for HR HPV detection combined with liquid-based cytology. Women with cytological abnormalities or HR HPV-positive results underwent colposcopy and cervical biopsy. This study demonstrated good overall agreement between HC II and real-time fluorescent PCR assay (overall agreement, 92.25%; Cohen's kappa=0.814). For the detection of high-grade cervical intraepithelial neoplasias (CIN) and CC, the sensitivity of HC II and real-time fluorescent PCR was 94.48 and 92.82%, respectively, and the negative predictive value was 98.85 and 98.54%, respectively. High HR HPV infection rate of the high-grade CIN and CC group was detected (P<0.05). In conclusion, real-time fluorescent PCR assay provides similar results compared to the HC II test for HR HPV detection and could be used in CC screening in clinic. FAU - Cheng, Jiaoying AU - Cheng J AD - Department of Gynecology and Obstetrics, China-Japan Friendship Hospital, Beijing 100029, P.R. China. FAU - Bian, Meilu AU - Bian M AD - Department of Gynecology and Obstetrics, China-Japan Friendship Hospital, Beijing 100029, P.R. China. FAU - Cong, Xiao AU - Cong X AD - Department of Gynecology and Obstetrics, China-Japan Friendship Hospital, Beijing 100029, P.R. China. FAU - Sun, Aiping AU - Sun A AD - Department of Gynecology and Obstetrics, China-Japan Friendship Hospital, Beijing 100029, P.R. China. FAU - Li, Min AU - Li M AD - Department of Gynecology and Obstetrics, China-Japan Friendship Hospital, Beijing 100029, P.R. China. FAU - Ma, Li AU - Ma L AD - Department of Gynecology and Obstetrics, China-Japan Friendship Hospital, Beijing 100029, P.R. China. FAU - Chen, Ying AU - Chen Y AD - Department of Gynecology and Obstetrics, China-Japan Friendship Hospital, Beijing 100029, P.R. China. FAU - Liu, Jun AU - Liu J AD - Department of Gynecology and Obstetrics, China-Japan Friendship Hospital, Beijing 100029, P.R. China. LA - eng PT - Journal Article DEP - 20121217 PL - England TA - Biomed Rep JT - Biomedical reports JID - 101613227 PMC - PMC3956221 OTO - NOTNLM OT - cervical cancer OT - human papillomavirus OT - hybrid capture II OT - real-time fluorescent polymerase chain reaction EDAT- 2014/03/22 06:00 MHDA- 2014/03/22 06:01 PMCR- 2012/12/17 CRDT- 2014/03/21 06:00 PHST- 2012/09/17 00:00 [received] PHST- 2012/10/18 00:00 [accepted] PHST- 2014/03/21 06:00 [entrez] PHST- 2014/03/22 06:00 [pubmed] PHST- 2014/03/22 06:01 [medline] PHST- 2012/12/17 00:00 [pmc-release] AID - br-01-02-0280 [pii] AID - 10.3892/br.2012.49 [doi] PST - ppublish SO - Biomed Rep. 2013 Mar;1(2):280-284. doi: 10.3892/br.2012.49. Epub 2012 Dec 17.