Novel cardiovascular risk factors in premature coronary atherosclerosis associated with systemic lupus erythematosus

J Rheumatol. 2008 Sep;35(9):1789-94. Epub 2008 Jul 15.

Abstract

Objective: Several mediators of inflammation are associated with atherosclerotic cardiovascular disease in the general population, but their relationship to accelerated atherosclerosis associated with an inflammatory disease such as systemic lupus erythematosus (SLE) is not known.

Methods: We compared concentrations of cytokines (TNF-alpha, IL-1alpha, and VEGF), inflammatory enzymes (MPO and MMP-9), acute-phase reactants (ESR, CRP, and SAA) and adhesion molecules (VCAM, ICAM, and E-selectin) in 109 patients with SLE and 78 controls. The relationship between inflammatory markers and coronary atherosclerosis detected as calcified plaque by electron beam CT was determined in patients with SLE.

Results: Concentrations of all markers of inflammation other than VCAM, MMP-9, and IL-1alpha were significantly higher in SLE. In multivariable analyses adjusting for Framingham risk score, cumulative corticosteroid dose, and diabetes, E-selectin (OR 1.90, 95% CI 1.08-3.33), VCAM (OR 1.99, 1.18-3.37), ICAM (OR 2.30, 1.13-4.7), and TNF-alpha (OR 2.36, 1.10-5.06) were significantly associated with the severity of coronary calcium.

Conclusion: Concentrations of adhesion molecules and TNF-alpha are associated with coronary atherosclerosis in SLE independent of the Framingham risk score.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Acute-Phase Proteins / analysis
  • Adult
  • Biomarkers / blood
  • Cell Adhesion Molecules / blood
  • Comorbidity
  • Coronary Artery Disease / blood*
  • Coronary Artery Disease / etiology
  • Cross-Sectional Studies
  • Cytokines / blood
  • Female
  • Humans
  • Inflammation Mediators / blood*
  • Lupus Erythematosus, Systemic / blood*
  • Lupus Erythematosus, Systemic / complications
  • Male
  • Risk Factors
  • Tumor Necrosis Factor-alpha / blood
  • Young Adult

Substances

  • Acute-Phase Proteins
  • Biomarkers
  • Cell Adhesion Molecules
  • Cytokines
  • Inflammation Mediators
  • Tumor Necrosis Factor-alpha