Endothelial cell biomarkers in critically ill COVID-19 patients with encephalitis

Victor Altmayer1,2,3, Jason Ziveri4, Corinne Frère1,5,6

  • 1Sorbonne Université, AP-HP.Sorbonne Université, Faculté de Médecine, Hôpital de la Pitié-Salpêtrière, Paris, France.

Journal of Neurochemistry
|November 25, 2021
PubMed

Insights

COVID-19 encephalitis involves endothelial activation, with angiopoietin-like 4 (ANGPTL4) uniquely elevated and potentially predicting brain dysfunction in critically ill patients.

Area of Science:

  • Neurology
  • Critical Care Medicine
  • Immunology

Background:

  • COVID-19 can cause encephalitis in critically ill patients.
  • Endothelial dysfunction is implicated in severe COVID-19 neurological complications.
  • Identifying biomarkers for COVID-19 encephalitis is crucial.

Purpose of the Study:

  • To determine the key markers of endothelial activation in COVID-19-related encephalitis.
  • To compare vascular biomarkers between COVID-19 patients with and without encephalitis.
  • To investigate the role of angiopoietin-like 4 (ANGPTL4) in this context.

Main Methods:

  • Observational study in an intensive care unit (ICU).
  • Comparison of vascular biomarkers in critically ill COVID-19 patients with (n=11) and without (n=21) encephalitis.
  • Encephalitis diagnosis based on new central neurologic symptoms and pathological brain MRI/EEG findings.

Main Results:

  • Encephalitis patients had significantly longer ICU stays (52 vs. 20.5 days).
  • Elevated levels of soluble endothelial activation markers (sE-selectin, TNF-α, IL-6, PLGF, thrombomodulin) were observed, correlated with TNF-α.
  • Angiopoietin-like 4 (ANGPTL4) was significantly higher in encephalitis patients and not correlated with TNF-α.

Conclusions:

  • COVID-19-related encephalitis is linked to cytokine-associated acute brain dysfunction.
  • Elevated ANGPTL4, independent of systemic inflammation, may serve as a predictor for encephalitis in critically ill COVID-19 patients.