Accelerated ageing is associated with increased Covid-19 severity and differences across ethnic groups may exist
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Published version
Author(s)
Reeves, Joshua J
Kooner, Jaspal S
Zhang, Weihua
Type
Journal Article
Abstract
Background:
While increased age is an established risk factor for COVID-19, there is great heterogeneity in outcomes within age groups. This is
because chronological age does not reflect health, unlike biological age. We intend to investigate the association between
accelerated ageing and COVID-19 outcomes through the lens of three measures, namely phenotypic age acceleration
(PhenoAgeAccel), telomere length (Adjusted T/S Ratio) and facial ageing, and to examine whether there are differences across
ethnic groups.
Methods:
Taking participants from the UK Biobank, we associated accelerated ageing with severe COVID-19 outcomes, defined as COVID-
related hospitalisation or death. Separate logistic regressions models were created for age and the three accelerated ageing-
related variables, adjusting for a variety of covariates in each model. Multivariable logistic regression models were also created
within White, Black, Asian and Other ethnic groups to assess for potential differing associations. Forward likelihood ratio logistic
regression models were created to evaluate importance of the variables and to assess for patterns of association across the total
population and ethnic groups.
Results:
After adjusting for all covariates, the odds ratio (OR) and 95% confidence interval (95% CI) of COVID-19 severe outcomes for age was
1.080 (1.074-1.086). After further adjusting age for the accelerated ageing variables, the ORs were 1.029 (1.020-1.039) for
PhenoAgeAccel and 0.847 (0.772-0.929) for Facial Ageing’s ‘Younger Than You Are’ while Adjusted T/S ratio and ‘Older Than You Are’
were statistically insignificant. The OR for age remained similar across ethnic groups. Both PhenoAgeAccel and younger facial ages
in the White population and PhenoAgeAccel in the Black population had ORs of 1.031 (1.021-1.042), 0.853 (0.774-0.939), and 1.049
(1.001-1.100), respectively. Both Adjusted T/S Ratio and older facial ages showed statistical insignificance in all ethnicities. In
forward logistic regression, age and PhenoAgeAccel were the age-related variables selected most frequently in all models.
Interpretation:
Accelerated ageing is associated with increased COVID-19 severity. The mechanisms at work here are likely immunosenescence and
inflamaging. This association indicates that anti-ageing treatment may improve COVID-19 outcome. The results within ethnic
groups and that of telomere length were inconclusive, but point to a need for future, more focused research on the topic.
While increased age is an established risk factor for COVID-19, there is great heterogeneity in outcomes within age groups. This is
because chronological age does not reflect health, unlike biological age. We intend to investigate the association between
accelerated ageing and COVID-19 outcomes through the lens of three measures, namely phenotypic age acceleration
(PhenoAgeAccel), telomere length (Adjusted T/S Ratio) and facial ageing, and to examine whether there are differences across
ethnic groups.
Methods:
Taking participants from the UK Biobank, we associated accelerated ageing with severe COVID-19 outcomes, defined as COVID-
related hospitalisation or death. Separate logistic regressions models were created for age and the three accelerated ageing-
related variables, adjusting for a variety of covariates in each model. Multivariable logistic regression models were also created
within White, Black, Asian and Other ethnic groups to assess for potential differing associations. Forward likelihood ratio logistic
regression models were created to evaluate importance of the variables and to assess for patterns of association across the total
population and ethnic groups.
Results:
After adjusting for all covariates, the odds ratio (OR) and 95% confidence interval (95% CI) of COVID-19 severe outcomes for age was
1.080 (1.074-1.086). After further adjusting age for the accelerated ageing variables, the ORs were 1.029 (1.020-1.039) for
PhenoAgeAccel and 0.847 (0.772-0.929) for Facial Ageing’s ‘Younger Than You Are’ while Adjusted T/S ratio and ‘Older Than You Are’
were statistically insignificant. The OR for age remained similar across ethnic groups. Both PhenoAgeAccel and younger facial ages
in the White population and PhenoAgeAccel in the Black population had ORs of 1.031 (1.021-1.042), 0.853 (0.774-0.939), and 1.049
(1.001-1.100), respectively. Both Adjusted T/S Ratio and older facial ages showed statistical insignificance in all ethnicities. In
forward logistic regression, age and PhenoAgeAccel were the age-related variables selected most frequently in all models.
Interpretation:
Accelerated ageing is associated with increased COVID-19 severity. The mechanisms at work here are likely immunosenescence and
inflamaging. This association indicates that anti-ageing treatment may improve COVID-19 outcome. The results within ethnic
groups and that of telomere length were inconclusive, but point to a need for future, more focused research on the topic.
Date Issued
2022-12-13
Date Acceptance
2022-11-21
Citation
Frontiers in Public Health, 2022, 10, pp.1-12
ISSN
2296-2565
Publisher
Frontiers Media
Start Page
1
End Page
12
Journal / Book Title
Frontiers in Public Health
Volume
10
Copyright Statement
Copyright © 2022 Reeves, Kooner and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
License URL
Identifier
https://www.frontiersin.org/articles/10.3389/fpubh.2022.1034227/full
Publication Status
Published
Article Number
1034227
Date Publish Online
2022-12-13