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Myocardial Injury in Post Mortem Biopsies of Patients with COVID-19

Authors :
Lidia Zytinsky Moura
Larissa Hermann de Souza Nunes
Anna Flavia Ribeiro dos Santos Miggiolaro
Caroline Busatta Vaz de Paula
Cristina Pellegrino Baena
José Rocha Faria Neto
Jarbas da Silva Motta Junior
Lucas Baena Carstens
Camila Hartmann
Gustavo Lenci Marques
Lucia de Noronha
Publication Year :
2020
Publisher :
Research Square Platform LLC, 2020.

Abstract

Background: Myocardial injury is significantly and independently associated with mortality in COVID-19 patients. However, the pathogenesis of myocardial injury in COVID-19 is still not clear, and cardiac involvement by SARS-CoV-2 remains a major challenge worldwide.Aim: This histopathological and immunohistochemical study seeks to clarify the pathogenesis of myocardial injury in COVID-19.Methods: Postmortem minimally invasive autopsies were performed in two patients who died from COVID-19, and the myocardium samples were compared to a control patient. Immunohistochemistry (IHC) staining was performed using monoclonal antibodies against the following targets: caspase-1, ICAM-1, TNF-α, IL-4, IL-6, CD163, TGF-β, MMP-9, type 1 and type 3 collagen.Results: The histopathological analysis showed severe pericellular interstitial edema surrounding each of the cardiomyocytes. The IHC analysis showed increased expression of caspase-1, ICAM-1, IL-4, IL-6, CD163, MMP-9 and type 3 collagen in the COVID-19 patients compared to the control. On the other hand, no difference from the control was observed in expression of TNF-α, TGF-β and type 1 collagen. Conclusion: Our findings point to a pathogenesis related with pyroptosis leading to endothelial disfunction. The subsequent inflammation with associated interstitial edema could explain the myocardial disfunction and arrythmias in COVID-19 patients. The presence of Th2 response, MMP-9 and type-3 collagen suggests progression to myocardial fibrosis in the long term.

Details

Database :
OpenAIRE
Accession number :
edsair.doi...........416caadc499a654df80197f57c5d67d8