21Jun 2023
Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder

Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder

A recent study published in Respiratory Research examines the association between COVID-19 and ultra-rare variants in the RTEL1 gene, which is linked to shorter telomere length. The patients exhibited higher liver function indices, increased levels of CRP and inflammatory markers, and a higher prevalence of autoimmune disorders compared to control subjects. The study suggests that RTEL1 variants could serve as predictive markers for COVID-19 severity and pulmonary fibrosis progression.

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