Persistent Endothelial Lung Damage and Impaired Diffusion Capacity in Long COVID

Author:

Asimakos Andreas T.1,Vassiliou Alice G.1ORCID,Keskinidou Chrysi1ORCID,Spetsioti Stavroula1ORCID,Antonoglou Archontoula1,Vrettou Charikleia S.1ORCID,Mourelatos Panagiotis2,Diamantopoulos Aristidis2,Pratikaki Maria3,Athanasiou Nikolaos1ORCID,Jahaj Edison1ORCID,Gallos Parisis4ORCID,Kotanidou Anastasia1ORCID,Dimopoulou Ioanna1ORCID,Orfanos Stylianos E.1,Katsaounou Paraskevi1ORCID

Affiliation:

1. First Department of Critical Care Medicine & Pulmonary Services, School of Medicine, National and Kapodistrian University of Athens, Evangelismos Hospital, 106 76 Athens, Greece

2. Department of Endocrinology Diabetes and Metabolism, National Expertise Center for Rare Endocrine Diseases, Evangelismos Hospital, 106 76 Athens, Greece

3. Biochemical Department, Evangelismos Hospital, 106 76 Athens, Greece

4. Computational Biomedicine Laboratory, Department of Digital Systems, University of Piraeus, 185 34 Piraeus, Greece

Abstract

Since the beginning of the pandemic, both COVID-19-associated coagulopathy biomarkers and a plethora of endothelial biomarkers have been proposed and tested as prognostic tools of severity and mortality prediction. As the pandemic is gradually being controlled, attention is now focusing on the long-term sequelae of COVID-19. In the present study, we investigated the role of endothelial activation/dysfunction in long COVID syndrome. This observational study included 68 consecutive long COVID patients and a healthy age and sex-matched control group. In both groups, we measured 13 endothelial biomarkers. Moreover, in the long COVID patients, we evaluated fatigue and dyspnea severity, lung diffusion capacity (DLCO), and the 6-min walk (6MWT) test as measures of functional capacity. Our results showed that markers of endothelial activation/dysfunction were higher in long COVID patients, and that soluble intracellular adhesion molecule 1 (sICAM-1) and soluble vascular adhesion molecule 1 (sVCAM-1) negatively correlated with lung diffusion and functional capacity (sICAM-1 vs. DLCO, r = −0.306, p = 0.018; vs. 6MWT, r = −0.263, p = 0.044; and sVCAM-1 vs. DLCO, r= −0.346, p = 0.008; vs. 6MWT, r = −0.504, p < 0.0001). In conclusion, evaluating endothelial biomarkers alongside clinical tests might yield more specific insights into the pathophysiological mechanisms of long COVID manifestations.

Publisher

MDPI AG

Subject

Medicine (miscellaneous)

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