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Epidemiological, clinical and viral determinants of the increased prevalence of high-risk human papillomavirus (HPV) infections in elderly women
1Department of Oncology and Radiotherapy, Turku University Hospital, Turku, Finland
2Department of Oral Pathology, Institute of Dentistry, and MediCity Research Laboratory, University of Turku, Finland
3N.N. Blokhin Cancer Research Centre of Russian Academy of Medical Sciences (RAMS), Moscow, Russia
4Russian Academy of Post-Graduate Medical Education, Moscow, Russia
5Novgorod Clinical Regional Hospital, Centralised Cytology Laboratory, Novgorod, Russia
6Novgorod Municipal Dermato-venereological Dispensary, Department of Gynaecology, Novgorod, Russia
7Novgorod Female Consultative Outpatient Hospital, Department of Gynaecology, Novgorod, Russia
8Research Institute of Oncology and Medical Radiology, Republican Centre of Clinical Cytology, Minsk, Belarus
9Minsk State Medical Institute, Department of Gynaecology and Obstetrics, Minsk, Belarus
10Latvian Cancer Centre, Department of Gynaecology, and Laboratory of Cytology, Riga, Latvia
11Department of Human Pathology and Oncology, University of Siena, Italy
*Corresponding Author(s): K. Syrjänen E-mail: kari.syrjanen@tyks.fi
Background: Population-based studies have reported a second peak of human papillomavirus (HPV) prevalence among women > 55 years, but reasons for this U-shaped HPV prevalence curve are poorly understood. Objectives: To analyse determinants of high-risk HPV (HR-HPV) infections among postmenopausal women. Study design and Methods: A cohort of 3,187 women was stratified into three age categories: i) youngest age group < 25 years (n = 1.103); ii) women between 26-55 years (n = 2.004), and iii) women > 55 years (n = 80), analysed for epidemiological, clinical and virological determinants of their HR-HPV infections. Real-time PCR was used for HPV genotyping, analysis of viral loads for HPV 16, 18/45, 31, 33/52/58, 35 and 39, and load of integrated HPV 16. Results: Age-standardised prevalence of HR-HPV infections showed a second peak among women > 55 years, with a perfect U-shaped curve (R(2) = 0.966). The factors explaining this increased HR-HPV prevalence among older women include: i) cohort effect, ii) higher viral loads for HR-HPV types with cubic model curve (R(2) = 0.714) for HPV 16, iii) distinct shift (p = 0.0001) from multiple-type infections to single HR-HPV types, iv) transition from episomal to integrated HPV 16 (p = 0.009), v) higher load of integrated HPV 16 (p = 0.009), and, vi) higher proportion of incident infections, higher rate of viral persistence, and lower rate of HR-HPV clearance. Conclusions: These data suggest that in women who fail to eradicate their HR-HPV infection until menopause, selection of integrated viral clone has taken place, driving the process towards progressing disease. Consequent to this, most of the HR-HPV infections in women > 55 years were associated with high-grade CIN or invasive carcinoma.
High-risk HPV; Postmenopause; Prevalence; Second peak; Predictors; Sexual behavior; Viral load; Integration; CIN, cervical cancer; Follow-up
K. Syrjänen,S.M. Kulmala,I. Shabalova,N. Petrovichev,V. Kozachenko,T. Zakharova,J. Pajanidi,J. Podistov,G. Chemeris,L. Sozaeva,E. Lipova,I. Tsidaeva,O. Ivanchenko,A. Pshepurko,S. Zakharenko,R. Nerovjna,L. Kljukina,M. Branovskaja,M. Nikitina,V. Grunjberga,A. Grunjberg,A. Juschenko,R. Santopietro,M. Cintorino,P. Tosi,S. Syrjänen. Epidemiological, clinical and viral determinants of the increased prevalence of high-risk human papillomavirus (HPV) infections in elderly women. European Journal of Gynaecological Oncology. 2008. 29(2);114-122.
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