Journal of Personalized Medicine (Aug 2023)

Persistent Endothelial Lung Damage and Impaired Diffusion Capacity in Long COVID

  • Andreas T. Asimakos,
  • Alice G. Vassiliou,
  • Chrysi Keskinidou,
  • Stavroula Spetsioti,
  • Archontoula Antonoglou,
  • Charikleia S. Vrettou,
  • Panagiotis Mourelatos,
  • Aristidis Diamantopoulos,
  • Maria Pratikaki,
  • Nikolaos Athanasiou,
  • Edison Jahaj,
  • Parisis Gallos,
  • Anastasia Kotanidou,
  • Ioanna Dimopoulou,
  • Stylianos E. Orfanos,
  • Paraskevi Katsaounou

DOI
https://doi.org/10.3390/jpm13091351
Journal volume & issue
Vol. 13, no. 9
p. 1351

Abstract

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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.

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