Persistent Endothelial Dysfunction in Coronavirus Disease-2019 Survivors Late After Recovery

Coronavirus disease 2019 (COVID-19) can result in an endothelial dysfunction in acute phase. However, information on the late vascular consequences of COVID-19 is limited. Brachial artery flow-mediated dilation (FMD) examination were performed, and inflammatory biomarkers were assessed in 86 survivo...

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Veröffentlicht in:Frontiers in medicine 2022-02, Vol.9, p.809033-809033
Hauptverfasser: Gao, Yi-Ping, Zhou, Wei, Huang, Pei-Na, Liu, Hong-Yun, Bi, Xiao-Jun, Zhu, Ying, Sun, Jie, Tang, Qiao-Ying, Li, Li, Zhang, Jun, Zhu, Wei-Hong, Cheng, Xue-Qing, Liu, Ya-Ni, Deng, You-Bin
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Sprache:eng
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Zusammenfassung:Coronavirus disease 2019 (COVID-19) can result in an endothelial dysfunction in acute phase. However, information on the late vascular consequences of COVID-19 is limited. Brachial artery flow-mediated dilation (FMD) examination were performed, and inflammatory biomarkers were assessed in 86 survivors of COVID-19 for 327 days (IQR 318-337 days) after recovery. Comparisons were made with 28 age-matched and sex-matched healthy controls and 30 risk factor-matched patients. Brachial artery FMD was significantly lower in the survivors of COVID-19 than in the healthy controls and risk factor-matched controls [median (IQR) 7.7 (5.1-10.7)% for healthy controls, 6.9 (5.5-9.4)% for risk factor-matched controls, and 3.5(2.2-4.6)% for COVID-19, respectively, < 0.001]. The FMD was lower in 25 patients with elevated tumor necrosis factor (TNF)-α [2.7(1.2-3.9)] than in 61 patients without elevated TNF-α [3.8(2.6-5.3), = 0.012]. Furthermore, FMD was inversely correlated with serum concentration of TNF-α (r = -0.237, = 0.007). Survivors of COVID-19 have a reduced brachial artery FMD, which is inversely correlated with increased serum concentration of TNF-α. Prospective studies on the association of endothelial dysfunction with long-term cardiovascular outcomes, especially the early onset of atherosclerosis, are warranted in survivors of COVID-19.
ISSN:2296-858X
2296-858X
DOI:10.3389/fmed.2022.809033