Viruses (Apr 2023)

Inflammatory Response and Activation of Coagulation after COVID-19 Infection

  • Anna Glória Fonseca Teodoro,
  • Wellington Francisco Rodrigues,
  • Thais Soares Farnesi-de-Assunção,
  • Anna V. Bernardes e Borges,
  • Malu Mateus Santos Obata,
  • José Rodrigues do Carmo Neto,
  • Djalma A. Alves da Silva,
  • Leonardo E. Andrade-Silva,
  • Chamberttan S. Desidério,
  • Juliana C. Costa-Madeira,
  • Rafaela M. Barbosa,
  • Andrezza C. C. Hortolani Cunha,
  • Loren Q. Pereira,
  • Fernanda Bernadelli de Vito,
  • Sarah Cristina Sato Vaz Tanaka,
  • Fernanda R. Helmo,
  • Marcela Rezende Lemes,
  • Laís M. Barbosa,
  • Rafael O. Trevisan,
  • Fabiano V. Mundim,
  • Ana Carolina M. Oliveira-Scussel,
  • Paulo Roberto Resende Junior,
  • Ivan B. Monteiro,
  • Yulsef M. Ferreira,
  • Guilherme H. Machado,
  • Kennio Ferreira-Paim,
  • Hélio Moraes-Souza,
  • Carlo José Freire de Oliveira,
  • Virmondes Rodrigues Júnior,
  • Marcos Vinicius da Silva

DOI
https://doi.org/10.3390/v15040938
Journal volume & issue
Vol. 15, no. 4
p. 938

Abstract

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SARS-CoV-2 (COVID-19) infection is responsible for causing a disease with a wide spectrum of clinical presentations. Predisposition to thromboembolic disease due to excessive inflammation is also attributed to the disease. The objective of this study was to characterize the clinical and laboratory aspects of hospitalized patients, in addition to studying the pattern of serum cytokines, and associate them with the occurrence of thromboembolic events. Methodology: A retrospective cohort study with 97 COVID-19 patients hospitalized from April to August 2020 in the Triângulo Mineiro macro-region was carried out. A review of medical records was conducted to evaluate the clinical and laboratory aspects and the frequency of thrombosis, as well as the measurement of cytokines, in the groups that presented or did not present a thrombotic event. Results: There were seven confirmed cases of thrombotic occurrence in the cohort. A reduction in the time of prothrombin activity was observed in the group with thrombosis. Further, 27.8% of all patients had thrombocytopenia. In the group that had thrombotic events, the levels of IL1b, IL-10, and IL2 were higher (p < 0.05). Conclusions: In the studied sample, there was an increase in the inflammatory response in patients with thrombotic events, confirmed by the increase in cytokines. Furthermore, in this cohort, a link was observed between the IL-10 percentage and an increased chance of a thrombotic event.

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