Coronary Atherosclerosis Phenotypes in Focal and Diffuse Disease

Koshiro Sakai1, Takuya Mizukami2, Jonathon Leipsic3

  • 1Cardiovascular Center Aalst, OLV Clinic, Aalst, Belgium; Department of Medicine, Division of Cardiology, Showa University School of Medicine, Tokyo, Japan.

PubMed

Insights

Focal coronary artery disease (CAD) shows higher plaque burden and lipid-rich plaques with thin-cap fibroatheroma (TCFA), while diffuse CAD has more calcifications. This links plaque characteristics to coronary hemodynamics.

Area of Science:

  • Cardiovascular Medicine
  • Interventional Cardiology
  • Medical Imaging

Background:

  • The relationship between coronary hemodynamics and atherosclerotic plaque characteristics is not fully understood.
  • Differentiating between focal and diffuse coronary artery disease (CAD) based on hemodynamics is crucial for understanding plaque behavior.

Purpose of the Study:

  • To compare atherosclerotic plaque phenotypes in focal versus diffuse CAD, as defined by coronary hemodynamics.
  • To investigate the association between pullback pressure gradient (PPG) and plaque morphology.

Main Methods:

  • A multicenter, prospective study included 117 patients with functionally significant lesions (FFR ≤0.80).
  • Plaque analysis utilized coronary computed tomography angiography (CCTA) and optical coherence tomography (OCT).
  • CAD patterns were assessed using motorized FFR pullbacks, quantifying focal vs. diffuse disease by median PPG.

Main Results:

  • Focal CAD exhibited higher plaque burden (87% vs. 82%, P=0.003) on CCTA.
  • Diffuse CAD showed significantly more calcifications (Agatston score: 158 vs. 51, P=0.024).
  • OCT revealed a higher prevalence of lipid-rich plaques (37% vs. 4%, P=0.001) and TCFAs (47% vs. 10%, P=0.002) in focal CAD.

Conclusions:

  • Atherosclerotic plaque phenotypes are associated with intracoronary hemodynamics.
  • Focal CAD is characterized by higher plaque burden and lipid-rich plaques with TCFAs.
  • Diffuse CAD is associated with more prevalent calcifications, highlighting distinct hemodynamic-morphological patterns.
Abstract

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