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Article ; Online: Endothelial injury in COVID-19 and septic patients.

Hokama, Larissa Tami / Veiga, Alicia Dudy Müller / Menezes, Maria Clara Saad / Sardinha Pinto, Agnes Araujo / de Lima, Thais Martins / Ariga, Suely Kunimi Kubo / Barbeiro, Hermes Vieira / Barbeiro, Denise Frediani / de Lucena Moreira, Claudia / Stanzani, Gabriela / Brandao, Rodrigo Antonio / Marchini, Julio Flavio / Alencar, Julio Cesar / Marino, Lucas Oliveira / Gomez, Luz Marina / Souza, Heraldo P

Microvascular research

2021  Volume 140, Page(s) 104303

Abstract: Systemic inflammatory response, as observed in sepsis and severe COVID-19, may lead to endothelial damage. Therefore, we aim to compare the extent of endothelial injury and its relationship to inflammation in both diseases. We included patients diagnosed ...

Abstract Systemic inflammatory response, as observed in sepsis and severe COVID-19, may lead to endothelial damage. Therefore, we aim to compare the extent of endothelial injury and its relationship to inflammation in both diseases. We included patients diagnosed with sepsis (SEPSIS group, n = 21), mild COVID-19 (MILD group, n = 31), and severe COVID-19 (SEVERE group, n = 24). Clinical and routine laboratory data were obtained, circulating cytokines (INF-γ, TNF-α, and IL-10) and endothelial injury markers (E-Selectin, Tissue Factor (TF) and von Willebrand factor (vWF)) were measured. Compared to the SEPSIS group, patients with severe COVID-19 present similar clinical and laboratory data, except for lower circulating IL-10 and E-Selectin levels. Compared to the MILD group, patients in the SEVERE group showed higher levels of TNF-α, IL-10, and TF. There was no clear relationship between cytokines and endothelial injury markers among the three studied groups; however, in SEVERE COVID-19 patients, there is a positive relationship between INF-γ with TF and a negative relationship between IL-10 and vWF. In conclusion, COVID-19 and septic patients have a similar pattern of cytokines and endothelial dysfunction markers. These findings highlight the importance of endothelium dysfunction in COVID-19 and suggest that endothelium should be better evaluated as a therapeutic target for the disease.
MeSH term(s) Aged ; Aged, 80 and over ; Biomarkers ; Blood Cell Count ; C-Reactive Protein/analysis ; COVID-19/blood ; COVID-19/complications ; COVID-19/pathology ; COVID-19/physiopathology ; E-Selectin/blood ; Endothelium, Vascular/pathology ; Female ; Humans ; Interferon-gamma/blood ; Interleukin-10/blood ; Male ; Middle Aged ; Retrospective Studies ; SARS-CoV-2 ; Sepsis/blood ; Sepsis/complications ; Sepsis/pathology ; Sepsis/physiopathology ; Severity of Illness Index ; Systemic Inflammatory Response Syndrome/blood ; Systemic Inflammatory Response Syndrome/etiology ; Systemic Inflammatory Response Syndrome/physiopathology ; Thromboplastin/analysis ; Tumor Necrosis Factor-alpha/analysis ; von Willebrand Factor/analysis
Chemical Substances Biomarkers ; E-Selectin ; IL10 protein, human ; SELE protein, human ; Tumor Necrosis Factor-alpha ; von Willebrand Factor ; Interleukin-10 (130068-27-8) ; Interferon-gamma (82115-62-6) ; C-Reactive Protein (9007-41-4) ; Thromboplastin (9035-58-9)
Language English
Publishing date 2021-12-13
Publishing country United States
Document type Comparative Study ; Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID 80307-8
ISSN 1095-9319 ; 0026-2862
ISSN (online) 1095-9319
ISSN 0026-2862
DOI 10.1016/j.mvr.2021.104303
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