| Literature DB >> 34783228 |
Andrea Vianello1, Gabriella Guarnieri1, Fausto Braccioni1, Sara Lococo1, Beatrice Molena1, Antonella Cecchetto1, Chiara Giraudo2, Leonardo Bertagna De Marchi1, Marco Caminati3, Gianenrico Senna3.
Abstract
Pulmonary fibrosis (PF), a pathological outcome of chronic and acute interstitial lung diseases associated to compromised wound healing, is a key component of the "post-acute COVID-19 syndrome" that may severely complicate patients' clinical course. Although inconclusive, available data suggest that more than a third of hospitalized COVID-19 patients develop lung fibrotic abnormalities after their discharge from hospital. The pathogenesis of PF in patients recovering from a severe acute case of COVID-19 is complex, and several hypotheses have been formulated to explain its development. An analysis of the data that is presently available suggests that biomarkers of susceptibility could help to identify subjects with increased probability of developing PF and may represent a means to personalize the management of COVID-19's long-term effects. Our review highlights the importance of both patient-related and disease-related contributing risk factors for PF in COVID-19 survivors and makes it definitely clear the possible use of acute phase and follow-up biomarkers for identifying the patients at greatest risk of developing this disease.Entities:
Keywords: ACE2; COVID-19; biomarker; interleukin; pulmonary fibrosis
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Year: 2021 PMID: 34783228 DOI: 10.1515/cclm-2021-1021
Source DB: PubMed Journal: Clin Chem Lab Med ISSN: 1434-6621 Impact factor: 3.694