# Gender-based differences in telomere attrition and long-term respiratory dysfunction in COVID-19 ICU survivors one year post-infection: implications for aging-associated pulmonary decline

**Authors:** Raquel Behar-Lagares, Ana Virseda-Berdices, Óscar Martínez-González, Rafael Blancas, Eva Manteiga, Paula Muñoz-García, María J. Mallol Poyato, Jorge Molina del Pozo, Marcela Homez-Guzmán, María A. Alonso Fernández, Salvador Resino, Amanda Fernández-Rodríguez, María Ángeles Jiménez-Sousa

PMC · DOI: 10.3389/fimmu.2025.1681454 · 2026-01-06

## TL;DR

This study finds that telomere shortening in blood cells is linked to long-term lung problems in men and women who survived critical COVID-19, with gender-specific patterns.

## Contribution

The study identifies gender-specific associations between telomere attrition and long-term respiratory outcomes in post-ICU COVID-19 survivors.

## Key findings

- Women with shorter telomeres and a history of pronation had more persistent respiratory symptoms.
- Men with shorter telomeres were more likely to develop diffuse parenchymal lung disease.
- Telomere attrition was significantly linked to ICU interventions like IMV and prone positioning in both genders.

## Abstract

A significant proportion of COVID-19 Intensive Care Unit (ICU) survivors develop long-term respiratory complications, including pulmonary fibrosis. Telomere attrition, a marker of cellular senescence, has emerged as a potential biomarker for post-COVID-19 sequelae. This study investigated the association between peripheral blood relative telomere length (RTL) and long-term pulmonary outcomes in COVID-19 ICU survivors, with a specific focus on gender-specific differences.

ICU-admitted COVID-19 patients were followed for at least one year post-discharge. RTL was quantified from peripheral blood using monochromatic multiplex quantitative PCR (MMqPCR) at hospital admission and one-year post-discharge. Primary outcomes were respiratory symptoms and diffuse parenchymal lung disease (DPLD), assessed via imaging. Data were analyzed using gender-stratified generalized linear models, adjusted for clinical covariates.

At one year, 43.8% of patients reported respiratory symptoms and 23.9% developed DPLD. A total of 73 ICU survivors were included, with 51 men and 22 women. At one year, 43.8% of patients reported respiratory symptoms and 23.9% developed DPLD. Longitudinal analysis showed significant RTL shortening in both men and women who underwent IMV (p=0.011 and p=0.016, respectively), and in men who needed pronation during their ICU stay (p=0.037). Regarding one-year symptoms, in women, repeated-measures analysis showed an association with persistent respiratory symptoms, particularly in those who needed pronation during their ICU stay [adjusted arithmetic mean ratio (aAMR)=0.73) (95%CI=0.60-0.90); p=0.003]. At follow-up, women who had undergone pronation and had shorter RTL continued to show a higher prevalence of symptoms [aAMR= 0.66 (0.58-0.76); p< 0.001]. In contrast, men with shorter RTL at one-year post-discharge had an association with the presence of DPLD [aAMR = 0.64 (0.50-0.81); p = 0.001]. This association in men was significant particularly among those who required IMV [aAMR= 0.61 (0.49-0.76); p< 0.001] or prone positioning [aAMR= 0.56 (0.44-0.71); p= 0.016].

These findings underscore the role of telomere attrition as a sex-specific biomarker of aging-associated pulmonary vulnerability in the aftermath of critical COVID-19 illness. RTL may serve as a prognostic marker for long-term respiratory sequelae, potentially guiding risk stratification and individualized follow-up strategies in post-ICU COVID-19 survivors.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096), pulmonary fibrosis (MONDO:0002771)

## Full-text entities

- **Diseases:** infection (MESH:D007239), DPLD (MESH:D017563), pulmonary fibrosis (MESH:D011658), respiratory (MESH:D012131), COVID-19 (MESH:D000086382), respiratory complications (MESH:D012140), post-COVID-19 sequelae (MESH:D000094024), pulmonary decline (MESH:D060825)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12815838/full.md

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Source: https://tomesphere.com/paper/PMC12815838