Low-Grade Endotoxemia and Thrombosis in COVID-19

Clin Transl Gastroenterol. 2021 Jun 4;12(6):e00348. doi: 10.14309/ctg.0000000000000348.

Abstract

Introduction: Patients with community-acquired pneumonia display enhanced levels of lipopolysaccharides (LPS) compared with controls, suggesting that low-grade endotoxemia may be implicated in vascular disturbances. It is unknown whether this occurs in patients with coronavirus 2019 (COVID-19) and its impact on thrombotic complications.

Methods: We measured serum levels of zonulin, a marker of gut permeability, LPS, and D-dimer in 81 patients with COVID-19 and 81 healthy subjects; the occurrence of thrombotic events in COVID-19 during the intrahospital stay was registered.

Results: Serum LPS and zonulin were higher in patients with COVID-19 than in control subjects and, in COVID-19, significantly correlated (R = 0.513; P < 0.001). Among the 81 patients with COVID-19, 11 (14%) experienced thrombotic events in the arterial (n = 5) and venous circulation (n = 6) during a median follow-up of 18 days (interquartile range 11-27 days). A logistic regression analysis showed that LPS (P = 0.024) and D-dimer (P = 0.041) independently predicted thrombotic events.

Discussion: The study reports that low-grade endotoxemia is detectable in patients with COVID-19 and is associated with thrombotic events. The coexistence of low-grade endotoxemia with enhanced levels of zonulin may suggest enhanced gut permeability as an underlying mechanism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / blood
  • COVID-19* / blood
  • COVID-19* / complications
  • COVID-19* / physiopathology
  • Correlation of Data
  • Endotoxemia* / diagnosis
  • Endotoxemia* / metabolism
  • Endotoxemia* / virology
  • Female
  • Fibrin Fibrinogen Degradation Products / analysis
  • Haptoglobins / metabolism*
  • Humans
  • Intestinal Mucosa* / metabolism
  • Intestinal Mucosa* / virology
  • Lipopolysaccharides / analysis
  • Male
  • Middle Aged
  • Permeability
  • Pneumonia, Viral / diagnosis
  • Pneumonia, Viral / etiology
  • Protein Precursors / metabolism*
  • SARS-CoV-2* / pathogenicity
  • SARS-CoV-2* / physiology
  • Thrombosis* / blood
  • Thrombosis* / diagnosis
  • Thrombosis* / etiology

Substances

  • Biomarkers
  • Fibrin Fibrinogen Degradation Products
  • Haptoglobins
  • Lipopolysaccharides
  • Protein Precursors
  • fibrin fragment D
  • zonulin