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Is COVID-19 severity associated with telomere length? A systematic review and meta-analysis

Telomere shortening, a marker of cellular aging, has been linked to hospitalization and the severity of COVID-19. In this systematic review and meta-analysis, the mean difference in telomere length between non-severe and severe COVID-19 individuals was pooled to determine the association between sho...

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Autores principales: Haridoss, Madhumitha, Ayyasamy, Lavanya, Bagepally, Bhavani Shankara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234232/
https://www.ncbi.nlm.nih.gov/pubmed/37261700
http://dx.doi.org/10.1007/s11262-023-02010-1
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author Haridoss, Madhumitha
Ayyasamy, Lavanya
Bagepally, Bhavani Shankara
author_facet Haridoss, Madhumitha
Ayyasamy, Lavanya
Bagepally, Bhavani Shankara
author_sort Haridoss, Madhumitha
collection PubMed
description Telomere shortening, a marker of cellular aging, has been linked to hospitalization and the severity of COVID-19. In this systematic review and meta-analysis, the mean difference in telomere length between non-severe and severe COVID-19 individuals was pooled to determine the association between short telomeres and COVID-19 severity. Relevant studies were retrieved through searches conducted in PubMed-Medline, Scopus, EMBASE, Medrxiv, Biorxiv, EuroPMC, and SSRN databases up to November 2022. Selected studies were systematically reviewed and assessed for risk of bias using AXIS tool. The standardized mean difference in telomere length between non-severe and severe COVID-19 was pooled using random-effects model. A total of thirteen studies were included in the review, out of which seven (1332 patients with the severe COVID-19 disease and 6321 patients with non-severe COVID-19) were eligible for meta-analysis. The estimated pooled mean difference in Leukocyte telomere length between severe COVID-19 and non-severe COVID-19 was 0.39 (95% CI − 0.02 to 0.81, I(2) = 93.5%) with substantial heterogeneity. Our findings do not provide clear evidence for association of shorter telomere length and severe COVID-19 disease. More extensive studies measuring absolute telomere length with age and gender adjustments are needed to draw definitive conclusions on the potential causal association between telomere shortening and COVID-19 severity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11262-023-02010-1.
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spelling pubmed-102342322023-06-01 Is COVID-19 severity associated with telomere length? A systematic review and meta-analysis Haridoss, Madhumitha Ayyasamy, Lavanya Bagepally, Bhavani Shankara Virus Genes Review Paper Telomere shortening, a marker of cellular aging, has been linked to hospitalization and the severity of COVID-19. In this systematic review and meta-analysis, the mean difference in telomere length between non-severe and severe COVID-19 individuals was pooled to determine the association between short telomeres and COVID-19 severity. Relevant studies were retrieved through searches conducted in PubMed-Medline, Scopus, EMBASE, Medrxiv, Biorxiv, EuroPMC, and SSRN databases up to November 2022. Selected studies were systematically reviewed and assessed for risk of bias using AXIS tool. The standardized mean difference in telomere length between non-severe and severe COVID-19 was pooled using random-effects model. A total of thirteen studies were included in the review, out of which seven (1332 patients with the severe COVID-19 disease and 6321 patients with non-severe COVID-19) were eligible for meta-analysis. The estimated pooled mean difference in Leukocyte telomere length between severe COVID-19 and non-severe COVID-19 was 0.39 (95% CI − 0.02 to 0.81, I(2) = 93.5%) with substantial heterogeneity. Our findings do not provide clear evidence for association of shorter telomere length and severe COVID-19 disease. More extensive studies measuring absolute telomere length with age and gender adjustments are needed to draw definitive conclusions on the potential causal association between telomere shortening and COVID-19 severity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11262-023-02010-1. Springer US 2023-06-01 /pmc/articles/PMC10234232/ /pubmed/37261700 http://dx.doi.org/10.1007/s11262-023-02010-1 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review Paper
Haridoss, Madhumitha
Ayyasamy, Lavanya
Bagepally, Bhavani Shankara
Is COVID-19 severity associated with telomere length? A systematic review and meta-analysis
title Is COVID-19 severity associated with telomere length? A systematic review and meta-analysis
title_full Is COVID-19 severity associated with telomere length? A systematic review and meta-analysis
title_fullStr Is COVID-19 severity associated with telomere length? A systematic review and meta-analysis
title_full_unstemmed Is COVID-19 severity associated with telomere length? A systematic review and meta-analysis
title_short Is COVID-19 severity associated with telomere length? A systematic review and meta-analysis
title_sort is covid-19 severity associated with telomere length? a systematic review and meta-analysis
topic Review Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234232/
https://www.ncbi.nlm.nih.gov/pubmed/37261700
http://dx.doi.org/10.1007/s11262-023-02010-1
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