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Coronary Atherosclerosis Phenotypes in Focal and Diffuse Disease.
Sakai, Koshiro; Mizukami, Takuya; Leipsic, Jonathon; Belmonte, Marta; Sonck, Jeroen; Nørgaard, Bjarne L; Otake, Hiromasa; Ko, Brian; Koo, Bon-Kwon; Maeng, Michael; Jensen, Jesper Møller; Buytaert, Dimitri; Munhoz, Daniel; Andreini, Daniele; Ohashi, Hirofumi; Shinke, Toshiro; Taylor, Charles A; Barbato, Emanuele; Johnson, Nils P; De Bruyne, Bernard; Collet, Carlos.
Affiliation
  • Sakai K; Cardiovascular Center Aalst, OLV Clinic, Aalst, Belgium; Department of Medicine, Division of Cardiology, Showa University School of Medicine, Tokyo, Japan.
  • Mizukami T; Cardiovascular Center Aalst, OLV Clinic, Aalst, Belgium; Division of Clinical Pharmacology, Department of Pharmacology, Showa University, Tokyo, Japan; Department of Cardiovascular Medicine, Gifu Heart Center, Gifu, Japan.
  • Leipsic J; Department of Medicine and Radiology, University of British Columbia, Vancouver, British Columbia, Canada.
  • Belmonte M; Cardiovascular Center Aalst, OLV Clinic, Aalst, Belgium; Department of Cardiology, University of Milan, Milan, Italy; Department of Advanced Biomedical Sciences, University Federico II, Naples, Italy.
  • Sonck J; Cardiovascular Center Aalst, OLV Clinic, Aalst, Belgium; Department of Advanced Biomedical Sciences, University Federico II, Naples, Italy.
  • Nørgaard BL; Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.
  • Otake H; Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Kobe, Japan.
  • Ko B; Monash Cardiovascular Research Centre, Monash University and Monash Heart, Monash Health, Clayton, Victoria, Australia.
  • Koo BK; Department of Internal Medicine and Cardiovascular Center, Seoul National University Hospital, Seoul, South Korea.
  • Maeng M; Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.
  • Jensen JM; Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.
  • Buytaert D; Cardiovascular Center Aalst, OLV Clinic, Aalst, Belgium.
  • Munhoz D; Cardiovascular Center Aalst, OLV Clinic, Aalst, Belgium; Department of Advanced Biomedical Sciences, University Federico II, Naples, Italy; Department of Internal Medicine, Discipline of Cardiology, University of Campinas (Unicamp), Campinas, Brazil.
  • Andreini D; Centro Cardiologico Monzino, IRCCS, Milan, Italy; Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
  • Ohashi H; Cardiovascular Center Aalst, OLV Clinic, Aalst, Belgium; Department of Cardiology, Aichi Medical University, Aichi, Japan.
  • Shinke T; Department of Medicine, Division of Cardiology, Showa University School of Medicine, Tokyo, Japan.
  • Taylor CA; HeartFlow, Inc, Redwood City, California, USA.
  • Barbato E; Cardiovascular Center Aalst, OLV Clinic, Aalst, Belgium; Department of Advanced Biomedical Sciences, University Federico II, Naples, Italy.
  • Johnson NP; Division of Cardiology, Department of Medicine, Weatherhead PET Center, McGovern Medical School, UTHealth and Memorial Hermann Hospital, Houston, Texas, USA.
  • De Bruyne B; Cardiovascular Center Aalst, OLV Clinic, Aalst, Belgium; Department of Cardiology, Lausanne University Hospital, Lausanne, Switzerland.
  • Collet C; Cardiovascular Center Aalst, OLV Clinic, Aalst, Belgium. Electronic address: carloscollet@gmail.com.
JACC Cardiovasc Imaging ; 16(11): 1452-1464, 2023 11.
Article in En | MEDLINE | ID: mdl-37480908
ABSTRACT

BACKGROUND:

The interplay between coronary hemodynamics and plaque characteristics remains poorly understood.

OBJECTIVES:

The aim of this study was to compare atherosclerotic plaque phenotypes between focal and diffuse coronary artery disease (CAD) defined by coronary hemodynamics.

METHODS:

This multicenter, prospective, single-arm study was conducted in 5 countries. Patients with functionally significant lesions based on an invasive fractional flow reserve ≤0.80 were included. Plaque analysis was performed by using coronary computed tomography angiography and optical coherence tomography. CAD patterns were assessed using motorized fractional flow reserve pullbacks and quantified by pullback pressure gradient (PPG). Focal and diffuse CAD was defined according to the median PPG value.

RESULTS:

A total of 117 patients (120 vessels) were included. The median PPG was 0.66 (IQR 0.54-0.75). According to coronary computed tomography angiography analysis, plaque burden was higher in patients with focal CAD (87% ± 8% focal vs 82% ± 10% diffuse; P = 0.003). Calcifications were significantly more prevalent in patients with diffuse CAD (Agatston score per vessel 51 [IQR 11-204] focal vs 158 [IQR 52-341] diffuse; P = 0.024). According to optical coherence tomography analysis, patients with focal CAD had a significantly higher prevalence of circumferential lipid-rich plaque (37% focal vs 4% diffuse; P = 0.001) and thin-cap fibroatheroma (TCFA) (47% focal vs 10% diffuse; P = 0.002). Focal disease defined by PPG predicted the presence of TCFA with an area under the curve of 0.73 (95% CI 0.58-0.87).

CONCLUSIONS:

Atherosclerotic plaque phenotypes associate with intracoronary hemodynamics. Focal CAD had a higher plaque burden and was predominantly lipid-rich with a high prevalence of TCFA, whereas calcifications were more prevalent in diffuse CAD. (Precise Percutaneous Coronary Intervention Plan [P3]; NCT03782688).
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Coronary Artery Disease / Fractional Flow Reserve, Myocardial / Plaque, Atherosclerotic Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: JACC Cardiovasc Imaging Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Coronary Artery Disease / Fractional Flow Reserve, Myocardial / Plaque, Atherosclerotic Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: JACC Cardiovasc Imaging Year: 2023 Document type: Article