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The impact of the human papillomavirus vaccine on high-grade cervical lesions in urban and rural areas: An age– period–cohort analysis

  • Jaimie Z. Shing
  • , Alicia Beeghly-Fadiel
  • , Marie R. Griffin
  • , Rachel S. Chang
  • , Staci L. Sudenga
  • , James C. Slaughter
  • , Manideepthi Pemmaraju
  • , Edward F. Mitchel
  • , Pamela C. Hull

Producción científica: Articlerevisión exhaustiva

3 Citas (Scopus)

Resumen

Disparities in human papillomavirus (HPV) vaccination exist between urban (metropoli-tan statistical areas (MSAs)) and rural (non-MSAs) regions. To address whether the HPV vaccine’s impact differs by urbanicity, we examined trends in cervical intraepithelial neoplasia grades 2 or 3 and adenocarcinoma in situ (collectively, CIN2+) incidence in MSAs and non-MSAs among Tennessee Medicaid (TennCare)-enrolled women aged 18–39 years and among the subset screened for cervical cancer in Tennessee, United States. Using TennCare claims data, we identified annual age-group-specific (18–20, 21–24, 25–29, 30–34, and 35–39 years) CIN2+ incidence (2008–2018). Joinpoint regression was used to identify trends over time. Age–period–cohort Poisson regression models were used to evaluate age, period, and cohort effects. All analyses were stratified by urbanicity (MSA versus non-MSA). From 2008–2018, 11,243 incident CIN2+ events (7956 in MSAs; 3287 in non-MSAs) were identified among TennCare-enrolled women aged 18–39 years. CIN2+ incident trends (2008–2018) were similar between women in MSAs and non-MSAs, with largest declines among ages 18–20 (MSA average annual percent change (AAPC):-30.4, 95% confidence interval (95%CI): −35.4, −25.0; non-MSA AAPC: −30.9, 95%CI: −36.8, −24.5) and 21–24 years (MSA AAPC:-14.8, 95%CI: −18.1, −11.3; non-MSA AAPC: −15.1, 95%CI: −17.9, −12.2). Significant declines for ages 18–20 years began in 2008 in MSAs compared to 2010 in non-MSAs. Trends were largely driven by age and cohort effects. These patterns were consistent among screened women. Despite evidence of HPV vaccine impact on reducing CIN2+ incidence regardless of urbanicity, significant declines in CIN2+ incidence were delayed in non-MSAs versus MSAs.

Idioma originalEnglish
Número de artículo4215
PublicaciónCancers
Volumen13
N.º16
DOI
EstadoPublished - ago 2 2021

Nota bibliográfica

Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.

Financiación

Funding: Jaimie Z. Shing reports grants from the National Institutes of Health (5TL1TR002244, R01CA20740). Alicia Beeghly-Fadiel reports pilot grants from the National Institutes of Health (U54CA163072, U54MD010722). Marie R. Griffin reports a grant from the Emerging Infections Co-operative Agreement from the Centers for Disease Control and Prevention (5U01C10003). Rachel S. Chang has no financial disclosures. Staci L. Sudenga reports a grant from National Cancer Institute (K07CA225404). James C. Slaughter has no financial disclosures. Manideepthi Pemmaraju reports a grant from the Emerging Infections Cooperative Agreement from the Centers for Disease Control and Prevention (5U01C10003). Edward F. Mitchel reports a grant from the Emerging Infections Co-operative Agreement from the Centers for Disease Control and Prevention (5U01C10003). Pamela C. Hull reports a grant from the National Institutes of Health (R01CA20740). The authors are indebted to the HPV-IMPACT Monitoring Project and the Tennessee Division of TennCare of the Department of Finance and Administration, who provided data. We would also like to thank Dr. Wanqing Wen, Vanderbilt University Medical Center, for providing initial programming assistance for the age?period?cohort analysis.Jaimie Z. Shing reports grants from the National Institutes of Health (5TL1TR002244, R01CA20740). Alicia Beeghly-Fadiel reports pilot grants from the National Institutes of Health (U54CA163072, U54MD010722). Marie R. Griffin reports a grant from the Emerging Infections Cooperative Agreement from the Centers for Disease Control and Prevention (5U01C10003). Rachel S. Chang has no financial disclosures. Staci L. Sudenga reports a grant from National Cancer Institute (K07CA225404). James C. Slaughter has no financial disclosures. Manideepthi Pemmaraju reports a grant from the Emerging Infections Cooperative Agreement from the Centers for Disease Control and Prevention (5U01C10003). Edward F. Mitchel reports a grant from the Emerging Infections Cooperative Agreement from the Centers for Disease Control and Prevention (5U01C10003). Pamela C. Hull reports a grant from the National Institutes of Health (R01CA20740).

FinanciadoresNúmero del financiador
Tennessee Division of TennCare of the Department of Finance and Administration
National Institutes of Health (NIH)U54CA163072, 5TL1TR002244, R01CA20740, U54MD010722
National Institutes of Health (NIH)
Centers for Disease Control and Prevention5U01C10003
Centers for Disease Control and Prevention
National Childhood Cancer Registry – National Cancer InstituteK07CA225404
National Childhood Cancer Registry – National Cancer Institute
Vanderbilt Digestive Diseases Research Center, Vanderbilt University Medical Center

    ODS de las Naciones Unidas

    Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

    1. Good health and well being
      Good health and well being

    ASJC Scopus subject areas

    • Oncology
    • Cancer Research

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