Publication:
Incorporating HPV 33 and Cytology Into HPV 16/18 Screening May Be Feasible. A Cross-Sectional Study

dc.authorscopusid56319544000
dc.contributor.authorTatar, Burak
dc.date.accessioned2025-12-11T00:31:28Z
dc.date.issued2023
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Tatar, Burak] Hlth Sci Univ, Samsun Res & Training Hosp, Dept Gynecol Oncol, Samsun, Turkey; [Tatar, Burak] Ondokuz Mayis Univ, Hlth Sci Inst, Dept Multidisciplinary Mol Med, Samsun, Turkeyen_US
dc.description.abstractPurpose The distribution of human papillomavirus (HPV) varies geographically, and each country is making its screening and vaccination program. This study questioned the need for colposcopy for HPV types other than HPV 16 and 18, and the need for cytology incorporated into HPV testing. Methods 1043 consecutive patients referred for colposcopy are included in this retrospective study. Logistic regression analysis, ANOVA, and Pearson's correlation were used for statistical analysis. The value of p < 0.05 was considered statistically significant. Results HPV 16 was the most common HPV type referred, followed by HPV 18, 52, 51, and 31, respectively. HPV 16 tends to be positive in younger patients than other HPV types (p < 0.05). Only HPV 16 (OR: 1.41, 1.06-1.88 95% CI) and HPV 33 (OR: 2.23; 1.06-4.64 95% CI) (p < 0.05) had significant prediction for CIN 2 + lesions. In patients with only a cytological abnormality, cytological abnormality with single other high-risk (hr) HPV (without HPV 16 or 18) or double other hrHPV positivity but without HPV 16 and 18 infections, we detected 159 (19%) CIN 2 + lesions. Conclusion HPV 33 may be implemented in hrHPV screening protocols for direct colposcopy referral as well as HPV 16 and HPV 18 in specific regions. If we had opted for HPV-based screening only for HPV 16 and 18 without cytology, 19% of all CIN 2 + lesions would have been missed. HPV-based screening only with HPV 16 and 18 may not be feasible. Nonavalent vaccines should be considered for the vaccination of specific populations.en_US
dc.description.woscitationindexScience Citation Index Expanded
dc.identifier.doi10.1007/s00404-022-06876-8
dc.identifier.endpage191en_US
dc.identifier.issn0932-0067
dc.identifier.issn1432-0711
dc.identifier.issue1en_US
dc.identifier.pmid36512112
dc.identifier.scopus2-s2.0-85143890698
dc.identifier.scopusqualityQ2
dc.identifier.startpage183en_US
dc.identifier.urihttps://doi.org/10.1007/s00404-022-06876-8
dc.identifier.urihttps://hdl.handle.net/20.500.12712/37012
dc.identifier.volume308en_US
dc.identifier.wosWOS:000898651200003
dc.identifier.wosqualityQ2
dc.institutionauthorTatar, Burak
dc.language.isoenen_US
dc.publisherSpringer Heidelbergen_US
dc.relation.ispartofArchives of Gynecology and Obstetricsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHPVen_US
dc.subjectHPV DNAen_US
dc.subjectCervical Cancer Screeningen_US
dc.subjectCytologyen_US
dc.titleIncorporating HPV 33 and Cytology Into HPV 16/18 Screening May Be Feasible. A Cross-Sectional Studyen_US
dc.typeArticleen_US
dspace.entity.typePublication

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