Association of monocyte subsets with vulnerability characteristics of coronary plaques as assessed by 64-slice multidetector computed tomography in patients with stable angina pectoris

Atherosclerosis. 2010 Sep;212(1):171-6. doi: 10.1016/j.atherosclerosis.2010.05.004. Epub 2010 May 11.

Abstract

Objective: The aim of the present study was to examine the relation between monocyte subsets and the presence, extent, and vulnerability characteristics of non-calcified coronary plaques (NCPs) as assessed by multidetector computed tomography (MDCT).

Methods: We studied 73 patients with stable angina pectoris who underwent MDCT. Two monocyte subsets (CD14(+)CD16(-) and CD14(+)CD16(+)) were measured by flow cytometry. Coronary artery plaques were assessed by 64-slice MDCT. We defined NCP vulnerability according to the presence of positive remodeling (remodeling index>1.05) and/or low CT attenuation plaques (<35 HU).

Results: A total of 40 (55%) patients had identifiable vulnerable plaques. The relative proportion of CD14(+)CD16(+) monocytes was significantly greater in patients with 1 or multiple vulnerable plaques than in patients with no vulnerable plaques or control (healthy) subjects. In addition, the relative proportion of CD14(+)CD16(+) monocytes was positively correlated with remodeling index (r=0.40, P<0.01) and negatively correlated with CT attenuation value (r=-0.34, P<0.01).

Conclusion: The present results suggest that an increased subset of CD14(+)CD16(+) monocytes is related to coronary plaque vulnerability in patients with stable angina pectoris.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Angina Pectoris / diagnostic imaging*
  • Angina Pectoris / etiology
  • Angina Pectoris / immunology*
  • Biomarkers / analysis
  • Case-Control Studies
  • Chi-Square Distribution
  • Coronary Angiography / methods*
  • Coronary Artery Disease / complications
  • Coronary Artery Disease / diagnostic imaging*
  • Coronary Artery Disease / immunology*
  • Disease Progression
  • Female
  • Flow Cytometry
  • GPI-Linked Proteins / analysis
  • Humans
  • Immunophenotyping
  • Japan
  • Linear Models
  • Lipopolysaccharide Receptors / analysis
  • Male
  • Middle Aged
  • Monocytes / immunology*
  • Phenotype
  • Predictive Value of Tests
  • Prognosis
  • Receptors, IgG / analysis
  • Risk Assessment
  • Risk Factors
  • Tomography, X-Ray Computed*
  • Up-Regulation

Substances

  • Biomarkers
  • FCGR3B protein, human
  • GPI-Linked Proteins
  • Lipopolysaccharide Receptors
  • Receptors, IgG