Post-reperfusion enhancement of CD14(+)CD16(-) monocytes and microvascular obstruction in ST-segment elevation acute myocardial infarction

Circ J. 2010 Jun;74(6):1175-82. doi: 10.1253/circj.cj-09-1045. Epub 2010 Apr 27.

Abstract

Background: The presence of microvascular obstruction (MVO) after primary ST-segment elevation acute myocardial infarction (STEMI) is associated with a poor outcome. The aim of the paper was to examine the relationship between distinct monocyte subsets and gadolinium-enhanced cardiovascular magnetic resonance (CMR) characteristics of MVO after STEMI.

Methods and results: Seventy-one patients with primary STEMI successfully treated with stenting were enrolled in the study. Two monocyte subsets (CD14(+)CD16(-) and CD14(+)CD16(+)) were measured on flow cytometry on admission and 2, 3, 4, 5, 8 days after the onset of STEMI. CMR was performed 7 days after revascularization to determine MVO on late gadolinium-enhanced imaging. The peak levels of CD14(+)CD16(-) monocytes, but not those of CD14(+)CD16(+) monocytes, were significantly higher in patients with MVO than in those without MVO. A multivariate logistic regression model showed that the post-perfusion peak levels of CD14(+)CD16(-) monocytes remained an independent factor for the presence of MVO (odds ratio=1.53; 95% confidence interval: 1.01-2.32; P=0.04). The absence of MVO was significantly associated with improvement in left ventricular ejection fraction.

Conclusions: Post-reperfusion enhancement of CD14(+)CD16(-) monocytes was associated with MVO in patients with STEMI. The pathophysiologic and therapeutic implications of this association require further study.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Coronary Thrombosis / diagnosis*
  • Female
  • Flow Cytometry
  • Gadolinium
  • Humans
  • Lipopolysaccharide Receptors*
  • Magnetic Resonance Angiography
  • Male
  • Microcirculation*
  • Middle Aged
  • Monocytes / pathology*
  • Myocardial Infarction / complications
  • Myocardial Infarction / pathology*
  • Receptors, IgG
  • Reperfusion

Substances

  • Lipopolysaccharide Receptors
  • Receptors, IgG
  • Gadolinium