Evidence map›Paper›PMID 40556866›Full record

ArticleFrontiers in aging2025

Telomere length and COVID-19 disease severity: insights from hospitalized patients.

Stijn Vos, Dries S Martens, Elien De Waele, Geert Dewyspelaere, Geert Mistiaen, Pieter Goeminne, Tim S Nawrot

Abstract read
In one paragraph

Article in Frontiers in aging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Stijn VosCentre for Environmental Sciences, Hasselt University, Hasselt, Belgium.
Dries S MartensCentre for Environmental Sciences, Hasselt University, Hasselt, Belgium.
Elien De WaeleVITAZ hospital Sint-Niklaas, Sint-Niklaas, Belgium.
Geert DewyspelaereVITAZ hospital Sint-Niklaas, Sint-Niklaas, Belgium.
Geert MistiaenVITAZ hospital Sint-Niklaas, Sint-Niklaas, Belgium.
Pieter GoeminneVITAZ hospital Sint-Niklaas, Sint-Niklaas, Belgium.
Tim S NawrotCentre for Environmental Sciences, Hasselt University, Hasselt, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Telomere length is associated with various disease and immune function and may therefore impact COVID-19 disease severity. We studied the associations between telomere length as a geroprotective susceptibility marker and clinical outcomes in hospitalized COVID-19 patients. Methods: 283 hospitalised COVID-19 patients (before vaccination, recruited between May 2020 and March 2021) were recruited for this cross-sectional study. Blood telomere length was determined by qPCR. The association between blood telomere length and clinical outcomes was examined using logistic regression, while adjusting for various covariates and confounders including demographic factors, comorbidity, body-mass index and blood cell counts. The primary clinical outcomes assessed were duration of stay, risk of ICU admission, and risk of requiring ventilation support. Results: Independent of sex and chronological age, an interquartile-range (IQR) increase in blood telomere length was associated with more favourable clinical outcomes in hospitalised COVID-19 patients: specifically, the odds ratio for ICU admission was 0.55 (95%CI: 0.32-0.88). Moreover, the odds ratio for the risk of ventilation was 0.52 (95%CI: 0.31-0.84). Finally, ordinal logistic regression revealed a lower odds for being in a higher quantile of hospital duration (OR: 0.79, 95%CI: 0.58-1.06). Discussion: To conclude, we found that in hospitalised COVID-19 patients, longer telomeres was associated with lower diseases severity in hospitalised COVID-19 patients, that could not be explained by shifts in blood cell counts. Therefore supporting the geroprotective or immunoprotective effects associated with longer telomeres conferring lower susceptibility to severe COVID-19 outcomes.

Indexed as

biological ageingCOVID-19COVID-19 severityrespiratory healthtelomere length

Identifiers

PMID40556866
PMCPMC12185540

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.