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Carotid intima-media thickness and flow-mediated dilation do not predict acute in-hospital outcomes in patients hospitalized with COVID-19.

Cristina-Oliveira, Michelle; Meireles, Kamila; Gil, Saulo; Cavalcante Assis, F�bio; Geber-J�nior, Jo�o Carlos; Shinjo, Samuel Katsuyuki; Possolo de Souza, Heraldo; Cruz Santana, Alfredo Nicodemos; Swinton, Paul A.; Drager, Luciano F.; Gualano, Bruno; Roschel, Hamilton; Pe�anha, Tiago

Authors

Michelle Cristina-Oliveira

Kamila Meireles

Saulo Gil

F�bio Cavalcante Assis

Jo�o Carlos Geber-J�nior

Samuel Katsuyuki Shinjo

Heraldo Possolo de Souza

Alfredo Nicodemos Cruz Santana

Luciano F. Drager

Bruno Gualano

Hamilton Roschel

Tiago Pe�anha



Abstract

Studies have suggested a potential role of endothelial dysfunction and atherosclerosis in the pathophysiology of COVID-19. Herein, we tested whether brachial flow-mediated dilation (FMD) and carotid intima-media thickness (cIMT) measured upon hospital admission are associated with acute in-hospital outcomes in patients hospitalized with COVID-19. A total of 211 patients hospitalized with COVID-19 were submitted to assessments of FMD and mean and maximum cIMT (cIMTmean and cIMTmax) within the first 72 h of hospital admission. Study primary outcome was a composite of intensive care unit admission, mechanical ventilation, or death during the hospitalization. These outcomes were also considered independently. Thrombotic events were included as a secondary outcome. Odds ratios (ORs) and confidence intervals (CIs) were calculated using unadjusted and adjusted multivariable logistic regression models. Eighty-eight (42%) participants demonstrated at least one of the composite outcomes. cIMTmean and cIMTmax were predictors of mortality and thrombotic events in the univariate analysis (cIMTmean and mortality: unadjusted OR 12.71 [95% CI 1.71-94.48]; P = 0.014; cIMTmean and thrombotic events: unadjusted OR 11.94 [95% CI 1.64-86.79]; P = 0.015; cIMTmax and mortality: unadjusted OR 8.47 [95% CI 1.41-51.05]; P = 0.021; cIMTmax and thrombotic events: unadjusted OR 12.19 [95% CI 2.03-73.09]; P = 0.007). However, these associations were no longer present after adjustment for potential confounders (P > 0.05). In addition, FMD% was not associated with any outcome. In conclusion, cIMT and FMD are not independent predictors of clinical outcomes in patients hospitalized with COVID-19. These results suggest that subclinical atherosclerosis and endothelial dysfunction may not be the main drivers of COVID-19 complications in patients hospitalized with COVID-19.NEW & NOTEWORTHY Studies have suggested a role of endothelial dysfunction and atherosclerosis in COVID-19 pathophysiology. In this prospective cohort study, we assessed the prognostic value of carotid intima-media thickness (IMT) and flow-mediated dilation (FMD) in patients with COVID-19. Carotid IMT and FMD were not independent predictors of major outcomes. These results suggest that other risk factors may be the main drivers of clinical outcomes in patients with COVID-19.

Citation

CRISTINA-OLIVEIRA, M., MEIRELES, K., GIL, S., CAVALCANTE ASSIS, F., GEBER-JÚNIOR, J.C., SHINJO, S.K., POSSOLO DE SOUZA, H., CRUZ SANTANA, A.N., SWINTON, P.A., DRAGER, L.F., GUALANO, B., ROSCHEL, H. and PEÇANHA, T. 2022. Carotid intima-media thickness and flow-mediated dilation do not predict acute in-hospital outcomes in patients hospitalized with COVID-19. American journal of physiology: heart and circulatory physiology [online], 322(6), pages H906-H913. Available from: https://doi.org/10.1152/ajpheart.00026.2022

Journal Article Type Article
Acceptance Date Mar 18, 2022
Online Publication Date Apr 22, 2022
Publication Date Jun 30, 2022
Deposit Date Mar 31, 2022
Publicly Available Date May 19, 2022
Journal American journal of physiology: heart and circulatory physiology
Print ISSN 0363-6135
Electronic ISSN 1522-1539
Publisher American Physiological Society
Peer Reviewed Peer Reviewed
Volume 322
Issue 6
Pages H906-H913
DOI https://doi.org/10.1152/ajpheart.00026.2022
Keywords Endothelium; Atherosclerosis; SARS-CoV-2; Mortality; Nitric oxide; Thrombosis; COVID-19
Public URL https://rgu-repository.worktribe.com/output/1628181

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