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The competing risk of death and selective survival cannot fully explain the inverse cancer-dementia association.
Hayes-Larson, Eleanor; Ackley, Sarah F; Zimmerman, Scott C; Ospina-Romero, Monica; Glymour, M Maria; Graff, Rebecca E; Witte, John S; Kobayashi, Lindsay C; Mayeda, Elizabeth Rose.
Afiliación
  • Hayes-Larson E; Department of Epidemiology, University of California, Los Angeles Fielding School of Public Health, Los Angeles, California, USA.
  • Ackley SF; Department of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.
  • Zimmerman SC; Department of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.
  • Ospina-Romero M; Department of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.
  • Glymour MM; Department of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.
  • Graff RE; Department of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.
  • Witte JS; Department of Epidemiology and Biostatistics, University of California, San Francisco, California, USA.
  • Kobayashi LC; Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, Michigan, USA.
  • Mayeda ER; Department of Epidemiology, University of California, Los Angeles Fielding School of Public Health, Los Angeles, California, USA.
Alzheimers Dement ; 16(12): 1696-1703, 2020 12.
Article en En | MEDLINE | ID: mdl-32881307
INTRODUCTION: We evaluated whether competing risk of death or selective survival could explain the reported inverse association between cancer history and dementia incidence (incidence rate ratio [IRR] ≈ 0.62-0.85). METHODS: A multistate simulation model of a cancer- and dementia-free cohort of 65-year-olds was parameterized with real-world data (cancer and dementia incidence, mortality), assuming no effect of cancer on dementia (true IRR = 1.00). To introduce competing risk of death, cancer history increased mortality. To introduce selective survival, we included a factor (prevalence ranging from 10% to 50%) that reduced cancer mortality and dementia incidence (IRRs ranged from 0.30 to 0.90). We calculated IRRs for cancer history on dementia incidence in the simulated cohorts. RESULTS: Competing risk of death yielded unbiased cancer-dementia IRRs. With selective survival, bias was small (IRRs = 0.89 to 0.99), even under extreme scenarios. DISCUSSION: The bias induced by selective survival in simulations was too small to explain the observed inverse cancer-dementia link, suggesting other mechanisms drive this association.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Simulación por Computador / Sesgo / Demencia / Neoplasias Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male Idioma: En Revista: Alzheimers Dement Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Simulación por Computador / Sesgo / Demencia / Neoplasias Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male Idioma: En Revista: Alzheimers Dement Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos