Comparative performance of hrHPV testing and PAX1/ZNF671 methylation in triaging women with abnormal cytology: a study of paired urine, vaginal and cervical scrape samples
Abstract
Background: The purpose was to evaluate the diagnostic effectiveness of High-risk human papillomavirus(hrHPV) testing, DNA methylation, PAX1/ZNF671 methylation in triaging patients with abnormal cytology and/or abnormal cervical biopsy pathology in cervical cancer screening; And the detection performance of different screening strategies was compared among clinician-taken cervical scrapes and paired self-collected urine and vaginal samples. Methods: A total of 136 urine-based,137self-collected vaginal and 140 cervical scrapes samples were analyzed. Samples were tested for hrHPV DNA and six methylation markers. Various screening strategies from different samples were compared under the definitive histopathology for their diagnostic accuracy against two standards: cervical intraepithelial neoplasia grade 2 or more severe lesions (CIN2+) and cervical intraepithelial neoplasia grade 3 or more severe lesions (CIN3+). Results: For PAX1 and ZNF671, the areas under the ROC curve were 0.929 and 0.862 and the methylation-positive rate was 89.5% (77/86) and 80.2% (69/86) in CIN3+ lesions. The cutoff values were 7.95and 10.92, respectively, with the highest Youden index values being 0.763 and 0.684, respectively. The sensitivity of hrHPV testing for CIN2+ was 89.80% in cervical scrape to 92.63% in self-collected vaginal samples. And the optimal marker panel (PAX1/ZNF671) resulted in an 85.8% sensitivity and 5.8 PLR for CIN2+ detection in cervical scrapes, and reached a highest sensitivity for CIN3+ in cervical scrapes (91.9%), markedly exceeding that of vaginal (71.4%) and urine (48.1%) samples (P
Fields of Study & Subjects
Cervical Cancer and HPV Research
Epigenetics and DNA Methylation
Women's cancer prevention and management
Publication details
- Journal / source
- Frontiers in Oncology
- Volume
- 16
- Pages
- 1765689–1765689
- Publication date
- 11 March 2026
- Language
- EN