The risk of fatality and/or severe complications due to COVID-19 infection is strongly age dependent. Data from the CDC suggests that those ages 85 and older have predicted mortality rates that is 100-fold higher than for those under the age of 50 and currently, 8 out of 10 COVID-19 deaths in the United States were in adults age 65 or older. While the exact etiology underlying this age disparity is unknown, evidence suggests that vulnerability may be due to changes that occur as a function of the aging process. This is further evidenced by the pattern of increased vulnerability among 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 determines risk, 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 DNA methylation levels at hundreds to thousands of CpG sites across the genome. Not only do epigenetic clocks track with age in diverse tissues and cell types, but discrepancies between epigenetic age and actual 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 these measures 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-19 susceptibility, and 2) advances in technology need to be made to ensure lower costs and rapid turnaround. This proposal aims to build on our team's multidisciplinary strengths to develop and validate a targeted, 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 treatment decisions in the clinic, to guiding social and pollical decisions when it comes to lifting ?stay-at-home? orders for certain individuals.

Public Health Relevance

The risks associated with COVID-19 infection are highly age and health dependent, suggesting that biological aging may be a major determinant for symptom severity and mortality risk. Based on our previous work in developing biomarkers of aging, we propose to develop and validate a novel, rapid, and affordable COVID-19 test to predict long-term response to infection, based on DNA methylation.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Transition Award (R00)
Project #
3R00AG052604-04S1
Application #
10158592
Study Section
Program Officer
Guo, Max
Project Start
2017-03-01
Project End
2021-05-31
Budget Start
2020-09-08
Budget End
2021-05-31
Support Year
4
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Yale University
Department
Pathology
Type
Schools of Medicine
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Levine, Morgan E; Crimmins, Eileen M (2018) Is 60 the New 50? Examining Changes in Biological Age Over the Past Two Decades. Demography 55:387-402