Association of monocyte subset counts with coronary fibrous cap thickness in patients with unstable angina pectoris

Atherosclerosis. 2010 Oct;212(2):628-35. doi: 10.1016/j.atherosclerosis.2010.06.025. Epub 2010 Jun 19.

Abstract

Objectives: We examined whether distinct monocyte subsets relate in specific ways to coronary fibrous cap thickness (FCT) in patients with unstable angina pectoris (UAP).

Methods: Forty patients with UAP who underwent percutaneous coronary intervention were enrolled in this study. The changes in the non-culprit FCT were assessed by optical coherence tomography (OCT) at baseline and after 9 months. The distinct monocyte subsets (CD14+CD16-CCR2+ and CD14+CD16+CX3CR1+) were measured by flow cytometry.

Results: The percent change in FCT showed significantly negative correlation with the percent changes in CD14+CD16+CX3CR1+ monocytes, but not CD14+CD16-CCR2+ monocytes. In addition, the percent change in CD14+CD16+CX3CR1+ monocytes was significantly decreased in the group of patients who received statin treatment compared with the group of patients who did not. Of interest, there was a close relationship between CD14+CD16+CX3CR1+ monocytes and levels of C-reactive protein, but not lipid profiles, including low-density lipoprotein cholesterol and low-/high-density lipoprotein cholesterol ratio.

Conclusions: CD14+CD16+CX3CR1+ monocytes may have a role in coronary plaque vulnerability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Angina, Unstable / blood*
  • Angina, Unstable / pathology
  • Angioplasty, Balloon, Coronary / methods
  • Blood Cell Count
  • CX3C Chemokine Receptor 1
  • Female
  • Humans
  • Lipids / chemistry
  • Lipopolysaccharide Receptors / biosynthesis
  • Male
  • Middle Aged
  • Monocytes / cytology*
  • Monocytes / metabolism
  • Myocardium / pathology
  • Receptors, CCR2 / biosynthesis
  • Receptors, Chemokine / biosynthesis
  • Receptors, IgG / biosynthesis

Substances

  • CX3C Chemokine Receptor 1
  • CX3CR1 protein, human
  • Lipids
  • Lipopolysaccharide Receptors
  • Receptors, CCR2
  • Receptors, Chemokine
  • Receptors, IgG