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dc.contributor.authorOzdemir, Cem Yagmur
dc.contributor.authorMarangoz, Bahar
dc.contributor.authorOzdemir, Nagihan
dc.contributor.authorCicekli, Nayif
dc.contributor.authorAbaci, Belgin
dc.contributor.authorArioz, Dagistan Tolga
dc.date.accessioned2025-12-28T16:39:51Z
dc.date.available2025-12-28T16:39:51Z
dc.date.issued2025
dc.identifier.issn8755-1039
dc.identifier.issn1097-0339
dc.identifier.urihttps://doi.org/10.1002/dc.70061
dc.identifier.urihttps://hdl.handle.net/20.500.12933/2148
dc.description.abstractObjective To describe the long-term clinical outcomes of women diagnosed with human papillomavirus type 31 (HPV 31) infection and to assess its potential implications for genotype-specific cervical cancer risk stratification in a real-world screening setting.Methods This retrospective cohort study analyzed 106,450 women screened for cervical cancer at the Afyonkarahisar Cancer Early Diagnosis, Screening, and Education Center (KETEM) between 2015 and 2025. Among 3313 HPV-positive women, 147 cases with confirmed HPV 31 infection and complete follow-up data were included. Clinical outcomes, cytology results, and histopathological findings were compared across three groups: isolated HPV 31, HPV 31 co-infected with HPV 16/18, and HPV 31 co-infected with other high-risk genotypes.Results Biopsies were performed in 66 women (44.9%) due to abnormal cytology or HPV 16/18 co-infection. CIN2+ lesions were detected in 15 patients (22.7% of those biopsied; 10.2% of the entire cohort). The CIN2+ detection rate was 6.0% in isolated HPV 31 infections and 44.4% in women co-infected with HPV 16/18 (p = 0.0006). Notably, 13.9% of cytology-negative women were diagnosed with CIN2+ on histopathology. Two invasive cancers occurred in women with isolated HPV 31 infection and negative cytology at baseline.Conclusion HPV 31 infection demonstrated measurable oncogenic potential, particularly in cytology-negative women and those with HPV 16/18 co-infection. While isolated HPV 31 positivity alone may not warrant immediate colposcopy, these findings support the need for genotype-specific risk stratification in cervical cancer screening. Further multicenter and prospective studies are required to confirm these results.
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofDiagnostic Cytopathology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectcervical cancer
dc.subjectgenotype-specific screening
dc.subjectHPV 31
dc.subjecthuman papillomavirus
dc.subjectrisk stratification
dc.titleClinical Outcomes and Risk Implications of HPV 31 Infection: A 10-Year Retrospective Cohort Study
dc.typeArticle
dc.departmentAfyonkarahisar Sağlık Bilimleri Üniversitesi
dc.identifier.doi10.1002/dc.70061
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.department-temp[Ozdemir, Cem Yagmur] Afyonkarahisar State Hosp, Dept Gynecol Oncol, Afyonkarahisar, Turkiye; [Marangoz, Bahar] Bolu Abant Izzet Baysal Univ, Dept Publ Hlth, Bolu, Turkiye; [Ozdemir, Nagihan] Afyonkarahisar Hlth Sci Univ, Fac Med, Dept Dermatol, Afyonkarahisar, Turkiye; [Cicekli, Nayif] Erzurum City Hosp, Dept Gynecol Oncol, Erzurum, Turkiye; [Abaci, Belgin] Afyonkarahisar State Hosp, Dept Afyonkarahisar Canc Early Diag Screening & Ed, Afyonkarahisar, Turkiye; [Arioz, Dagistan Tolga] Afyonkarahisar Hlth Sci Univ, Fac Med, Dept Gynecol Oncol, Afyonkarahisar, Turkiye
dc.identifier.pmid41346095
dc.identifier.scopus2-s2.0-105024012064
dc.identifier.scopusqualityN/A
dc.identifier.wosWOS:001630898900001
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.snmzKA_WoS_20251227


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