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Biological Aging Predicts Vulnerability to COVID-19 Severity in UK Biobank Participants.
Kuo, Chia-Ling; Pilling, Luke C; Atkins, Janice L; Masoli, Jane A H; Delgado, João; Tignanelli, Christopher; Kuchel, George A; Melzer, David; Beckman, Kenneth B; Levine, Morgan E.
  • Kuo CL; Connecticut Convergence Institute for Translation in Regenerative Engineering, University of Connecticut Health, Farmington, USA.
  • Pilling LC; University of Connecticut Center on Aging, School of Medicine, Farmington, USA.
  • Atkins JL; University of Connecticut Center on Aging, School of Medicine, Farmington, USA.
  • Masoli JAH; College of Medicine and Health, University of Exeter, UK.
  • Delgado J; College of Medicine and Health, University of Exeter, UK.
  • Tignanelli C; College of Medicine and Health, University of Exeter, UK.
  • Kuchel GA; College of Medicine and Health, University of Exeter, UK.
  • Melzer D; Department of Surgery, University of Minnesota, Minneapolis, USA.
  • Beckman KB; University of Connecticut Center on Aging, School of Medicine, Farmington, USA.
  • Levine ME; University of Connecticut Center on Aging, School of Medicine, Farmington, USA.
J Gerontol A Biol Sci Med Sci ; 76(8): e133-e141, 2021 07 13.
Article in English | MEDLINE | ID: covidwho-1120179
ABSTRACT

BACKGROUND:

Age and disease prevalence are the 2 biggest risk factors for Coronavirus disease 2019 (COVID-19) symptom severity and death. We therefore hypothesized that increased biological age, beyond chronological age, may be driving disease-related trends in COVID-19 severity.

METHODS:

Using the UK Biobank England data, we tested whether a biological age estimate (PhenoAge) measured more than a decade prior to the COVID-19 pandemic was predictive of 2 COVID-19 severity outcomes (inpatient test positivity and COVID-19-related mortality with inpatient test-confirmed COVID-19). Logistic regression models were used with adjustment for age at the pandemic, sex, ethnicity, baseline assessment centers, and preexisting diseases/conditions.

RESULTS:

Six hundred and thirteen participants tested positive at inpatient settings between March 16 and April 27, 2020, 154 of whom succumbed to COVID-19. PhenoAge was associated with increased risks of inpatient test positivity and COVID-19-related mortality (ORMortality = 1.63 per 5 years, 95% CI 1.43-1.86, p = 4.7 × 10-13) adjusting for demographics including age at the pandemic. Further adjustment for preexisting diseases/conditions at baseline (ORM = 1.50, 95% CI 1.30-1.73 per 5 years, p = 3.1 × 10-8) and at the early pandemic (ORM = 1.21, 95% CI 1.04-1.40 per 5 years, p = .011) decreased the association.

CONCLUSIONS:

PhenoAge measured in 2006-2010 was associated with COVID-19 severity outcomes more than 10 years later. These associations were partly accounted for by prevalent chronic diseases proximate to COVID-19 infection. Overall, our results suggest that aging biomarkers, like PhenoAge may capture long-term vulnerability to diseases like COVID-19, even before the accumulation of age-related comorbid conditions.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Severity of Illness Index / Aging / Mortality / Biological Specimen Banks / COVID-19 Testing / COVID-19 Type of study: Diagnostic study / Observational study / Prognostic study Topics: Long Covid Limits: Aged / Humans / Middle aged Country/Region as subject: Europa Language: English Journal: J Gerontol A Biol Sci Med Sci Journal subject: Geriatrics Year: 2021 Document Type: Article Affiliation country: Gerona

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Severity of Illness Index / Aging / Mortality / Biological Specimen Banks / COVID-19 Testing / COVID-19 Type of study: Diagnostic study / Observational study / Prognostic study Topics: Long Covid Limits: Aged / Humans / Middle aged Country/Region as subject: Europa Language: English Journal: J Gerontol A Biol Sci Med Sci Journal subject: Geriatrics Year: 2021 Document Type: Article Affiliation country: Gerona