Frontiers in Cardiovascular Medicine (Jun 2024)

Risk factors and prognostic value of endotoxemia in patients with acute myocardial infarction

  • Maxime Nguyen,
  • Maxime Nguyen,
  • Alain Putot,
  • Alain Putot,
  • Alain Putot,
  • David Masson,
  • Yves Cottin,
  • Thomas Gautier,
  • Laura Tribouillard,
  • Anne-Laure Rérole,
  • Pierre-Grégoire Guinot,
  • Pierre-Grégoire Guinot,
  • Maud Maza,
  • Jean-Paul Pais de Barros,
  • Valérie Deckert,
  • Michel Farnier,
  • Laurent Lagrost,
  • Marianne Zeller,
  • Marianne Zeller

DOI
https://doi.org/10.3389/fcvm.2024.1419001
Journal volume & issue
Vol. 11

Abstract

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BackgroundThere is increasing evidence regarding the association between endotoxemia and the pathogenesis of atherosclerosis and myocardial infarction (MI). During the acute phase of MI, endotoxemia might increase inflammation and drive adverse cardiovascular (CV) outcomes. We aimed to explore the risk factors and prognostic value of endotoxemia in patients admitted for acute MI.MethodsPatients admitted to the coronary care unit of Dijon University Hospital for type 1 acute MI between 2013 and 2015 were included. Endotoxemia, assessed by plasma lipopolysaccharide (LPS) concentration, was measured by mass spectrometry. Major adverse CV events were recorded in the year following hospital admission.ResultsData from 245 consecutive MI patients were analyzed. LPS concentration at admission markedly increased with age and diabetes. High LPS concentration was correlated with metabolic biomarkers (glycemia, triglyceride, and total cholesterol) but not with CV (troponin Ic peak and N-terminal pro-brain natriuretic peptide) or inflammatory biomarkers (C-reactive protein, IL6, IL8, and TNFα). LPS concentration was not associated with in-hospital or 1-year outcomes.ConclusionsIn patients admitted for MI, higher levels of endotoxins were related to pre-existing conditions rather than acute clinical severity. Therefore, endotoxins measured on the day of MI could reflect metabolic chronic endotoxemia rather than MI-related acute gut translocation.

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