Interleukin-10 serum levels and systemic endothelial vasoreactivity in patients with coronary artery disease

Stephan Fichtlscherer1, Susanne Breuer, Christopher Heeschen

  • 1Department of Internal Medicine IV, Division of Cardiology, Johann W. Goethe University, Frankfurt, Germany. fichtlscherer@em.uni-frankfurt.de

Insights

Elevated interleukin-10 (IL-10) serum levels correlate with improved endothelial vasoreactivity in coronary artery disease (CAD) patients, especially those with high C-reactive protein (CRP). This highlights the role of inflammatory balance in endothelial function.

Area of Science:

  • Cardiovascular Medicine
  • Immunology
  • Vascular Biology

Background:

  • Chronic inflammation drives atherosclerosis progression.
  • Interleukin-10 (IL-10) is an anti-inflammatory cytokine with protective effects in experimental atherosclerosis.
  • The endothelium is a primary target for inflammatory cytokines.

Purpose of the Study:

  • To investigate the association between elevated serum IL-10 levels and improved endothelial vasoreactivity in patients with coronary artery disease (CAD).

Main Methods:

  • Forearm blood flow (FBF) responses were measured in 65 male CAD patients.
  • Endothelium-dependent (acetylcholine) and endothelium-independent (sodium nitroprusside) vasoreactivity were assessed using venous occlusion plethysmography.

Main Results:

  • Serum IL-10 levels positively correlated with acetylcholine-induced FBF responses (r = 0.31, p < 0.02).
  • No significant correlation was found with sodium nitroprusside responses.
  • Elevated IL-10 levels were associated with preserved acetylcholine-stimulated FBF in patients with high C-reactive protein (CRP).
  • IL-10 and CRP serum levels were independent predictors of acetylcholine-induced FBF responses on multivariate analysis.

Conclusions:

  • Increased serum IL-10 levels are linked to enhanced systemic endothelial vasoreactivity in CAD patients, particularly those with elevated CRP.
  • The balance between pro-inflammatory and anti-inflammatory mediators significantly influences endothelial function in CAD.
Abstract

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