CD14+CD16+ monocytes in coronary artery disease and their relationship to serum TNF-alpha levels

Thromb Haemost. 2004 Aug;92(2):419-24. doi: 10.1160/TH04-02-0095.

Abstract

Monocytes play a central role in the inflammatory disease atherosclerosis. CD14+CD16+ monocytes are considered proinflammatory monocytes, as they have an increased capacity to produce proinflammatory cytokines, such as TNF-alpha, and are elevated in various inflammatory diseases. We hypothesized that patients with coronary artery disease (CAD) have increased levels of CD14+CD16+ monocytes, and that CD14+CD16+ monocytes are associated with inflammation markers. We investigated CD14+CD16+ monocytes in 247 patients with CAD and 61 control subjects using flow cytometry. In addition serum concentrations of TNF-alpha, IL-6, and Hs-CRP were assessed. Patients with CAD had higher levels of CD14+CD16+ monocytes than controls (13.6% versus 11.4%; p<0.001). Logistic regression analysis including quartiles of CD14+CD16+ monocytes showed that CD14+CD16+ monocytes were associated with prevalence of CAD (OR 4.9, 95% CI 2.5-19.1, for subjects in the fourth quartile in comparison to subjects in the first quartile). The association between CD14+CD16+ monocytes and CAD remained independently significant after adjustment for most potential confounders (OR 5.0, 95% CI 1.2-20.0). Serum concentrations of TNF-alpha were elevated in subjects within the highest quartiles of CD14+CD16+ monocytes (p=0.018). Our study showed that increased numbers of CD14+CD16+ monocytes are associated with coronary atherosclerosis and TNF-alpha. In accordance, recent animal studies suggest a possibly important role of these monocytes in the development of atherosclerosis.

MeSH terms

  • Aged
  • Analysis of Variance
  • Antibodies, Monoclonal / metabolism
  • Arteriosclerosis / pathology
  • Body Mass Index
  • Case-Control Studies
  • Cell Separation
  • Coronary Artery Disease / blood
  • Coronary Artery Disease / metabolism*
  • Female
  • Flow Cytometry
  • Humans
  • Inflammation
  • Interleukin-6 / metabolism
  • Lipopolysaccharide Receptors / biosynthesis*
  • Logistic Models
  • Male
  • Middle Aged
  • Monocytes / metabolism
  • Odds Ratio
  • Receptors, IgG / biosynthesis*
  • Risk Factors
  • Tumor Necrosis Factor-alpha / biosynthesis*

Substances

  • Antibodies, Monoclonal
  • Interleukin-6
  • Lipopolysaccharide Receptors
  • Receptors, IgG
  • Tumor Necrosis Factor-alpha