AI Article Synopsis

  • COVID-19 survivors exhibit a higher risk of pulmonary fibrosis, but the specific molecular processes behind this condition remain unclear.* -
  • In a study involving 12 COVID-19 patients who died from respiratory failure, researchers analyzed gene expression profiles compared to 11 healthy individuals to understand how pulmonary fibrosis develops over time.* -
  • Findings indicate that after the first week of hospitalization, patients shift from inflammation-related gene activity to fibrosis-related gene activity, suggesting potential targets for future treatment.*

Article Abstract

(1) Background: In COVID-19 survivors there is an increased prevalence of pulmonary fibrosis of which the underlying molecular mechanisms are poorly understood; (2) Methods: In this multicentric study, n = 12 patients who succumbed to COVID-19 due to progressive respiratory failure were assigned to an early and late group (death within ≤7 and >7 days of hospitalization, respectively) and compared to n = 11 healthy controls; mRNA and protein expression as well as biological pathway analysis were performed to gain insights into the evolution of pulmonary fibrogenesis in COVID-19; (3) Results: Median duration of hospitalization until death was 3 (IQR25-75, 3-3.75) and 14 (12.5-14) days in the early and late group, respectively. Fifty-eight out of 770 analyzed genes showed a significantly altered expression signature in COVID-19 compared to controls in a time-dependent manner. The entire study group showed an increased expression of and , independent of hospitalization time. In the early group there was increased activity of inflammation-related genes and pathways, while fibrosis-related genes (particularly ) and pathways dominated in the late group; (4) Conclusions: After the first week of hospitalization, there is a shift from pro-inflammatory to fibrogenic activity in severe COVID-19. and may serve as potential therapeutic targets in future studies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8835897PMC
http://dx.doi.org/10.3390/ijms23031583DOI Listing

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