Association of Microluminal Structures Assessed by Optical Coherence Tomography With Local Inflammation in Adjacent

Yutaka Kawabata1, Tetsuzo Wakatsuki1, Koji Yamaguchi1

  • 1Department of Cardiovascular Medicine, Tokushima University Graduate School of Biomedical Sciences.

Abstract

Insights

Coronary intraplaque microluminal structures (MS) are linked to vulnerable plaques and inflammation in epicardial adipose tissue (EAT). This study found MS are associated with lipid-rich plaques and EAT inflammation, suggesting a role in coronary artery disease progression.

Area of Science:

  • Cardiovascular Pathology
  • Atherosclerosis Research
  • Inflammation Biology

Background:

  • Coronary intraplaque microluminal structures (MS) are indicators of plaque vulnerability.
  • Vascular inflammation progresses inward from the adventitia to the intima.
  • The relationship between MS, epicardial adipose tissue (EAT) inflammation, and plaque characteristics requires further investigation.

Purpose of the Study:

  • To investigate the association between coronary intraplaque microluminal structures (MS).
  • To examine the link between local inflammation in adjacent epicardial adipose tissue (EAT).
  • To determine the relationship with coronary plaque characteristics.

Main Methods:

  • Optical coherence tomography (OCT) identified MS in coronary arteries from cadaveric hearts.
  • Lesions were categorized into MS-positive and MS-negative groups.
  • Inflammatory molecule levels in EAT and lipid volume were quantified.

Main Results:

  • MS-positive plaques showed significantly higher levels of vascular endothelial growth factor B and C-C motif chemokine ligand 2 in adjacent EAT.
  • Plaques with MS exhibited a significantly higher percentage of lipid volume.
  • These findings indicate a correlation between MS, EAT inflammation, and plaque lipid content.

Conclusions:

  • Intraplaque MS identified by OCT are associated with lipid-rich coronary plaques.
  • MS are linked to local inflammation in the adjacent epicardial adipose tissue (EAT).
  • These results suggest that EAT inflammation contributes to coronary plaque vulnerability through MS formation.