key: cord-0914881-vdmllq0t
authors: Vieceli Dalla Sega, Francesco; Fortini, Francesca; Spadaro, Savino; Ronzoni, Luca; Zucchetti, Ottavio; Manfrini, Marco; Mikus, Elisa; Fogagnolo, Alberto; Torsani, Francesca; Pavasini, Rita; Marracino, Luisa; Verri, Marco; Morandi, Luca; D'Aniello, Emanuele; Volta, Carlo Alberto; Campo, Gianluca; Ferrari, Roberto; Rizzo, Paola; Contoli, Marco
title: Time course of endothelial dysfunction markers and mortality in COVID‐19 patients: A pilot study
date: 2021-03-01
journal: Clin Transl Med
DOI: 10.1002/ctm2.283
sha: 1468a8d5232e6ce8b669cd5c626df27aa5a41761
doc_id: 914881
cord_uid: vdmllq0t

nan

To the Editor: Previous studies suggested that the endothelial dysfunction is associated with the severity and mortality of patients affected by coronavirus disease 2019 (COVID-19). However, the temporal evolution of markers of endothelial dysfunction during the progression of the disease and the relative relationship with the exitus are less established. 1, 2 The present study is a subanalysis from the "Prothrombotic status in patients with SARS-CoV-2 infection" study (ATTAC-Co, https://www.clinicaltrials.gov/ identifier NCT04343053) focused on biomarkers of endothelial dysfunction. The ATTAC-Co is a single-center, prospective study including 54 patients admitted to hospital for moderate-severe respiratory failure and positive for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. SARS-CoV-2 infection was confirmed by reverse transcriptase-polymerase chain reaction assay from nasopharyngeal swab specimen. In COVID-19 patients, symptoms appeared 9 ± 2 days before admission. The control group included 11 patients admitted to Pulmonology Unit with respiratory failure and negative to SARS-CoV-2 infection. Endothelial dysfunction biomarkers (endothelin-1, endoglin, sE-selectin, thrombomodulin, soluble vascular cell adhesion molecule 1 [sVCAM-1], and von Willebrand factor [vWF]) were measured in three different blood samples in COVID-19 patients (inclusion [T1], after 7 ± 2 days [T2], and 14 ± 2 days [T3]). These patients received 4000-8000 IU enoxaparin twice per day. On the contrary, one single blood sample withdrawal was performed at inclusion in controls. The aims of the present analysis were the comparison between cases versus controls, and between survivors versus nonsurvivors. The protocol was approved by the corresponding Ethics Committee, and all patients provided written informed consent. Details on the clinical trial, assays, and statistics are provided in the Supplementary Material. Table 1 reports clinical, laboratory, and biomarker data of control and COVID-19 patients at entry. Baseline characteristics did not differ between COVID-19 patients and (Table 1) . Table 2 summarizes the molecular function of endothelial dysfunction biomarkers. COVID-19 patients showed higher values of C-reactive protein, highsensitivity troponin, IL-6, and TNF-α. Regarding endothelial biomarkers, sVCAM-1 and thrombomodulin were significantly higher (Table 1 and Figure 1A ).

In the follow-up, 16 out of 54 (30%) COVID-19 patients died. As expected, several baseline characteristics and laboratory findings differed between nonsurvivors and survivors ( Table 1) . As reported by others, there was a higher frequency of CKD and higher levels of C-reactive protein, 3 but not higher number of current smokers in nonsurvivors compared to survivors. Different from other published studies, in our set of data PAD was more frequent among nonsurvivors. Endoglin and sVCAM-1 were significantly higher at inclusion in nonsurvivors versus survivors (Table 1 and Figure 1A ). Interestingly, sVCAM-1 in control versus nonsurvivors remains strongly significant, while it loses significance when only the survivors' group is compared to controls ( Figure 1A) . A similar trend is also observed for thrombomodulin ( Figure 1A ). This underlines the increase of these two biomarkers in the nonsurvivors' group. Figure 1B illustrates the time course of the biomarkers in survivors versus nonsurvivors corrected for potential confounding variables. In nonsurvivors, thrombomodulin and vWF significantly increased over time ( Figure 1B ). sVCAM-1 displayed a similar trend but without reaching statistical significance (P = .08) ( Figure 1B ). Consistent with other studies, we found high levels of vWF both in COVID-19 and controls compared to normal values. [4] [5] [6] Furthermore, vWF levels increased over time in nonsurvivors versus survivors, in agreement with other reports of high mortality and worse prognosis in patients with higher levels of vWF. 5, 7 In contrast, endothelin-1 remained stable in nonsurvivors but increased over time in survivors ( Figure 1B ). The remaining biomarkers of endothelial dysfunction did not show significant variations between survivors and nonsurvivors over their time courses ( Figure 1B 

Soluble endoglin Endoglin is a coreceptor of the transforming growth factor β receptor. It regulates vascular remodeling, angiogenesis, and the activity of endothelial nitric oxide synthase Soluble form of endoglin is released after shedding, and it is a marker of endothelial injury, activation, and inflammation Endothelin-1 Produced by vascular endothelial cells as a precursor is cleaved to be secreted in its active form. Endothelin-1 binds to its receptors exerting a potent vasoconstrictor Table S1 ). Univariate Cox regression analyses showed that endoglin, thrombomodulin, and sVCAM-1 levels were associated with death (Table S2 ). Multivariate analysis, including the variables associated with death on univariate analysis listed in Table S2 , revealed that only sVCAM-1 was independently associated with mortality (Table S2 ). Figure 2A shows that, on admission, patients with levels of sVCAM-1 higher than median (>1088 ng/mL) versus those with levels lower than median (<1088 ng/mL) have higher mortality rate. The predictive mortality value of sVCAM-1 is confirmed by the ROC analysis yielding in a high area under the curve (AUC = 0.823) ( Figure 2B ). This is true also for patients younger than 75 years ( Figure S1B ,C). Our data confirm and expand previous evidence on the role of endothelial dysfunction in COVID-19 patients. First, COVID-19 patients have higher levels of thrombomodulin and sVCAM-1 compared to controls with same clinical presentation but without SARS-CoV-2 infection. This supports the concept that COVID-19 pneumonia specifically affects the endothelium. 2 Second, endoglin, an adhesion molecule expressed by endothelial cells in response to inflammation, never investigated before in the context of COVID-19, is associated with death. Although multivariable analysis did not confirm its independent prognostic role, we believe that this finding further supports how the link between inflammatory storm and endothelial dysfunction should be considered crucial in COVID-19 pathogenesis. Third, sVCAM-1 is the only biomarker that, at multivariate analysis, remained independently associated to mortality. Older age is associated to increased cardiovascular comorbidities and is a risk factor for COVID-19 mortality. 8 However, sVCAM-1 predictive value is highlighted by survival and ROC analyses, and is maintained in younger patients (<75 years). The early increase of VCAM-1 may promote leukocytes recruitment, thus determining increased vascular permeability, tissue damage, and the release of further proinflammatory cytokines, all eventually contributing to mortality. These data have clinical implications. Dexamethasone in vitro contrasts the expression of sVCAM-1 in endothelial cells, 9 and the RECOVER trial showed that dexamethasone treatment reduces mortality in hospitalized COVID-19 patients. 10 It is plausible that dexamethasone reduces mortality, at least in part, also by contrasting sVCAM-1-induced endothelial activation and leukocyte recruitment. Fourth, surprisingly, endothelin-1 increased over time in COVID-19 survivors. This finding is counterintuitive as, under normal conditions, endothelin-1 participates in the regulation of vascular tone contrasting the effect of nitric oxide. Endothelin-1 is elevated in pulmonary arterial hypertension, a condition that is treated by endothelin-1 receptor antagonists. 11 Elevated pulmonary arterial hypertension has been observed in COVID-19 patients and the constant increase found in the survivors may be linked to this. 12 On the other hand, endothelin-1 is also linked to angiogenesis, 13 which has been observed in the lung of COVID-19 patients. 14 It is tempting to speculate that higher endothelin-1 levels promote angiogenesis in the survivors even though the clinical significance of angiogenesis in the lung of COVID-19 patients remains to be established.

Our report is just a proof-of-concept, hypothesisgenerating effort that has several limitations. The results are not applicable to asymptomatic or mild-symptomatic COVID-19 patients. Although we assessed three different time points, we cannot describe the alterations in endothelial function between viral infection and the admission to F I G U R E 2 A, Kaplan-Meier analysis. Patients were stratified by soluble vascular cell adhesion molecule 1 (sVCAM-1) median concentration in blood at hospital admission. Plot shows P-value of the log-rank test between groups. B, Time-dependent ROC analysis of sVCAM-1 blood concentration toward patients outcomes, showing area under the curve (AUC) with 95% confidence interval and its associated P-value the hospital. In addition, it should be noted that the sample size of our pilot study is small and further investigations in larger population are clearly on demand. Furthermore, this report focuses on endothelial dysfunction, thus the role of other cardiovascular parameters has not been discussed. In conclusion, we performed an analysis of a broad panel of biomarkers of endothelial dysfunction at different time points in COVID-19 patients. We observed important changes over time of the biomarkers, and in particular those of sVCAM-1 seem to be strongly related to mortality.

The authors declare that there is no conflict of interest.

The data that support the findings of this study are available from the corresponding author upon reasonable request.

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