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Genetic Variants in Genes Related to Lung Function and Interstitial Lung Diseases Are Associated with Worse Outcomes in Severe COVID-19 and Lung Performance in the Post-COVID-19 Condition.

International journal of molecular sciences2025-03-13PubMed
Total: 70.0Innovation: 7Impact: 7Rigor: 7Citation: 7

Summary

In 936 hospitalized COVID-19 patients, genetic variants in lung function and ILD-related genes were examined against severe outcomes (IMV requirement, ARDS classification) and mortality. In 102 post-COVID patients, serial pulmonary function tests over one year linked genetic background to longitudinal lung performance. Findings support shared pathogenic pathways between chronic respiratory gene networks and COVID-19 severity and recovery.

Key Findings

  • In 936 hospitalized COVID-19 patients, severe outcomes were assessed using IMV requirement, ARDS classification, and in-hospital mortality.
  • Variants in lung function and ILD genes were associated with worse acute outcomes and with lung performance during the post-COVID-19 condition (as per title).
  • A post-COVID cohort of 102 patients underwent pulmonary function testing four times over one year, enabling longitudinal association analyses.

Clinical Implications

Genetic markers may help identify patients at risk for severe respiratory failure (IMV/ARDS) and guide follow-up intensity after discharge, including targeted pulmonary rehabilitation.

Why It Matters

This study bridges human genetics of chronic lung disease with COVID-19 severity and post-acute recovery, enabling risk stratification and mechanistic hypotheses for ARDS in COVID-19.

Limitations

  • Specific variants and effect sizes are not detailed in the abstract
  • Potential confounding and population stratification; external validation not described

Future Directions

Independent replication across ancestries, functional validation of implicated variants/pathways, and development of polygenic risk tools integrating acute and long-term outcomes.

Study Information

Study Type
Cohort
Research Domain
Pathophysiology
Evidence Level
III - Observational cohort linking genetic variants to clinical outcomes and post-discharge lung function
Study Design
OTHER