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Estimating the Age of Disease-causal HPV Infection Based on the Natural History of CIN2+ Among Females in Canada Open Access.

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Názov: Estimating the Age of Disease-causal HPV Infection Based on the Natural History of CIN2+ Among Females in Canada Open Access.
Autori: Cherif, A, You, X, Hillhouse, E, Stone, R C, Murphy, B, Baluni, G, Yadav, M, Gotarkar, S, Reuschenbach, M, Chen, Y T, Cook, J, Roberts, C, Franco, E L
Zdroj: Open Forum Infectious Diseases; Apr2025, Vol. 12 Issue 4, p1-7, 7p
Predmety: DISCRETE event simulation, CERVICAL intraepithelial neoplasia, HUMAN papillomavirus, AGE distribution, OLDER women
Geografický termín: CANADA
Abstrakt: Background Although human papillomavirus (HPV) vaccination is approved for males and females up to 45 years of age in Canada, not all of the jurisdictions offer catch-up programs up to age 26. However, US-based modeling studies suggest a significant proportion of causal HPV infections leading to high-grade cervical intraepithelial neoplasia (CIN+) and cervical cancer occur in women older than age 26 years. To inform vaccination policies in Canada, this study estimated the age distribution of putatively causal HPV infections leading to CIN2+ based on the natural history. Methods We modified an existing discrete event simulation model to estimate the age of causal HPV infection for females diagnosed with CIN2+. Simulated females (n = 1000) were tracked through 3 stages while undergoing screening: causal HPV infection, CIN2+ disease onset, and diagnosis. We identified the age distribution for causal infections that best fit the observed age distribution for CIN2+ diagnosis. Ten independent model runs were conducted to assess reproducibility. Results The predicted median age at causal HPV infection and CIN2+ diagnosis in Canada was 24.9 (95% confidence interval, 24.3-26.1) and 29.8 years (95% confidence interval, 28.8-30.6), respectively. The model estimated that 84.1% and 47.1% of causal HPV infections occurred in women older than age 18 and 26 years, respectively. Results were stable across 10 model runs. Conclusions The analysis indicates a substantial percentage of causal HPV infections for CIN2+ occur among women aged 26 years or older. Extending catch-up vaccination programs to women above age 26 years should be considered to prevent these infections and reduce HPV-related cervical diseases. [ABSTRACT FROM AUTHOR]
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Databáza: Complementary Index
Popis
Abstrakt:Background Although human papillomavirus (HPV) vaccination is approved for males and females up to 45 years of age in Canada, not all of the jurisdictions offer catch-up programs up to age 26. However, US-based modeling studies suggest a significant proportion of causal HPV infections leading to high-grade cervical intraepithelial neoplasia (CIN+) and cervical cancer occur in women older than age 26 years. To inform vaccination policies in Canada, this study estimated the age distribution of putatively causal HPV infections leading to CIN2+ based on the natural history. Methods We modified an existing discrete event simulation model to estimate the age of causal HPV infection for females diagnosed with CIN2+. Simulated females (n = 1000) were tracked through 3 stages while undergoing screening: causal HPV infection, CIN2+ disease onset, and diagnosis. We identified the age distribution for causal infections that best fit the observed age distribution for CIN2+ diagnosis. Ten independent model runs were conducted to assess reproducibility. Results The predicted median age at causal HPV infection and CIN2+ diagnosis in Canada was 24.9 (95% confidence interval, 24.3-26.1) and 29.8 years (95% confidence interval, 28.8-30.6), respectively. The model estimated that 84.1% and 47.1% of causal HPV infections occurred in women older than age 18 and 26 years, respectively. Results were stable across 10 model runs. Conclusions The analysis indicates a substantial percentage of causal HPV infections for CIN2+ occur among women aged 26 years or older. Extending catch-up vaccination programs to women above age 26 years should be considered to prevent these infections and reduce HPV-related cervical diseases. [ABSTRACT FROM AUTHOR]
ISSN:23288957
DOI:10.1093/ofid/ofaf168