COVID-19 and Cohort Longevity: Causal Estimates from a Cohort Discontinuity Design

  • Funded by National Institutes of Health (NIH)
  • Total publications:0 publications

Grant number: 1R21AG086923-01

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Key facts

  • Disease

    COVID-19
  • Start & end year

    2024
    2026
  • Known Financial Commitments (USD)

    $271,362
  • Funder

    National Institutes of Health (NIH)
  • Principal Investigator

    PROFESSOR MICHEL GUILLOT
  • Research Location

    United States of America
  • Lead Research Institution

    UNIVERSITY OF PENNSYLVANIA
  • Research Priority Alignment

    N/A
  • Research Category

    Epidemiological studies

  • Research Subcategory

    Disease surveillance & mapping

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Unspecified

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

Project Summary In this R21, we propose a detailed study of Covid-19's impact on the mortality of single-year birth cohorts of males and females in France and the United States, with additional analyses by race for the United States. The findings from this R21 will complement existing studies of the mortality impact of Covid-19 that have almost exclusively adopted a period approach using measures such as period life expectancy. Our proposed analyses will combine important developments in the formal demography of cohort survivorship by Guillot and colleagues with a causal identification strategy employing a novel cohort discontinuity design developed by Wu, Mark, and colleagues to identify the causal effect of the Great Recession on U.S. fertility. Our analyses will provide credible causal estimates of: (1) the effect of Covid-19 on all-cause mortality for single-year birth cohorts of males and females in France and the United States, and for Black and White Americans in the United States; and (2) the degree to which the Covid-19 mortality shock has offset or reversed pre-pandemic progress in cohort survival. Our analyses will rely throughout on secondary data from French and U.S. vital registers that provide detailed, high quality data on all-cause mortality for single-year birth cohorts of males and females. Findings will break new ground by providing credible causal evidence relevant to ongoing mortality research and debates on racial disparities, health systems, pension schemes, and population dynamics.