Epigenetic Age Measures to Predict COVID-19 Symptom Progression and Severity

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

Grant number: 3R00AG052604-04S1

Grant search

Key facts

  • Disease

    COVID-19
  • Start & end year

    2017
    2021
  • Known Financial Commitments (USD)

    $139,448
  • Funder

    National Institutes of Health (NIH)
  • Principal Investigator

    Morgan Elyse Levine
  • Research Location

    United States of America
  • Lead Research Institution

    Yale University
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics

  • Research Subcategory

    Diagnostics

  • Special Interest Tags

    N/A

  • Study Type

    Non-Clinical

  • Clinical Trial Details

    N/A

  • Broad Policy Alignment

    Pending

  • Age Group

    Not Applicable

  • Vulnerable Population

    Not applicable

  • Occupations of Interest

    Not applicable

Abstract

PROJECT SUMMARY The risk of fatality and/or severe complications due to COVID-19 infection is strongly agedependent. Data from the CDC suggests that those ages 85 and older have predicted mortality ratesthat is 100-fold higher than for those under the age of 50 and currently, 8 out of 10 COVID-19 deathsin the United States were in adults age 65 or older. While the exact etiology underlying this agedisparity is unknown, evidence suggests that vulnerability may be due to changes that occur as afunction of the aging process. This is further evidenced by the pattern of increased vulnerabilityamong persons with pre-existing diseases of aging-cardiovascular disease, diabetes, COPD,chronic kidney disease, liver disease-suggesting that it isn't just chronological age that determinesrisk, but rather, biological age. In recent years, our group has helped develop some of the most robust biomarkers available,namely the epigenetic clocks. These measures estimate biological age in a sample based on DNAmethylation levels at hundreds to thousands of CpG sites across the genome. Not only do epigeneticclocks track with age in diverse tissues and cell types, but discrepancies between epigenetic age andactual age have also been shown to predict risk of mortality and incidence of major chronic disease,including those which appear to be major risk factors for COVID-19. However, in order for thesemeasures to be informative for assessing COVID-19 risk clinically, or in the general population, 1)they need to be re-optimized to capture the aspects of biological aging specific to COVID-19susceptibility, and 2) advances in technology need to be made to ensure lower costs and rapidturnaround. This proposal aims to build on our team's multidisciplinary strengths to develop and validate atargeted, lab-developed, readily-available test to predict COVID-19 symptomology and mortality risk.If successful, this test will have widespread applications-from informing triage and treatmentdecisions in the clinic, to guiding social and pollical decisions when it comes to lifting "stay-at-home"orders for certain individuals.