Microvascular Research | 2021
Biomarkers of endothelial dysfunction and outcomes in coronavirus disease 2019 (COVID-19) patients: A systematic review and meta-analysis
Abstract
\n Background\n Several studies have reported that the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can directly infect endothelial cells, and endothelial dysfunction is often found in severe cases of coronavirus disease 2019 (COVID-19). To better understand the prognostic values of endothelial dysfunction in COVID-19-associated coagulopathy, we conducted a systematic review and meta-analysis to assess biomarkers of endothelial cells in patients with COVID-19.\n \n Methods\n A literature search was conducted on online databases for observational studies evaluating biomarkers of endothelial dysfunction and composite poor outcomes in COVID-19 patients.\n \n Results\n A total of 1187 patients from 17 studies were included in this analysis. The estimated pooled means for von Willebrand Factor (VWF) antigen levels in COVID-19 patients was higher compared to healthy control (306.42 [95% confidence interval (CI) 291.37–321.48], p\u202f<\u202f0.001; I2:86%), with the highest VWF antigen levels was found in deceased COVID-19 patients (448.57 [95% CI 407.20–489.93], p\u202f<\u202f0.001; I2:0%). Meta-analysis showed that higher plasma levels of VWF antigen, tissue-type plasminogen activator (t-PA), plasminogen activator inhibitor-1 antigen (PAI-1) antigen, and soluble thrombomodulin (sTM) were associated with composite poor outcome in COVID-19 patients ([standardized mean difference (SMD) 0.74 [0.33–1.16], p\u202f<\u202f0.001; I2:80.4%], [SMD 0.55 [0.19–0.92], p\u202f=\u202f0.003; I2:6.4%], [SMD 0.33 [0.04–0.62], p\u202f=\u202f0.025; I2:7.9%], and [SMD 0.55 [0.10–0.99], p\u202f=\u202f0.015; I2:23.6%], respectively).\n \n Conclusion\n The estimated pooled means show increased levels of VWF antigen in COVID-19 patients. Several biomarkers of endothelial dysfunction, including VFW antigen, t-PA, PAI-1, and sTM, are significantly associated with increased composite poor outcomes in patients with COVID-19.\n \n PROSPERO registration number\n CRD42021228821.\n \n Unlabelled Table\n \n \n \n \n What is known about this topic?\n \n \n •\n The coronavirus disease 2019 (COVID-19) often manifests as cardiovascular complications such as myocarditis, myocardial injuries, arrhythmias, and venous thromboembolism events.\n \n \n •\n Recent evidence suggests that increased inflammatory cytokines, including interleukin-6 in patients with severe and critical COVID-19, are lower compared to patients with sepsis and ARDS not associated with COVID-19, thus questioning the role of a cytokine storm in COVID-19-related multiple organ damage.\n \n \n •\n Several studies have reported that the SARS-CoV-2 can directly infect endothelial cells, and endothelial dysfunction is often found in severe cases of COVID-19.\n \n \n \n \n \n What does this paper add?\n \n \n •\n The estimated pooled means for von Willebrand Factor (VWF) antigen levels in COVID-19 patients are higher compared to healthy control, with the highest VWF antigen levels are found in deceased COVID-19 patients.\n \n \n •\n Our meta-analysis shows that several biomarkers of endothelial dysfunction, including VFW antigen, tissue-type plasminogen activator (t-PA), plasminogen activator inhibitor-1 antigen (PAI-1) antigen, and soluble thrombomodulin (sTM), are significantly associated with increased composite poor outcome in patients with COVID-19.\n \n \n •\n Laboratory examination of VWF antigen, t-PA, PAI-1, and sTM plasma level may be useful for vascular risk assessment and predicting adverse outcomes and help guide therapy in COVID-19 patients.\n \n \n \n \n \n \n \n \n \n