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Updated: Jan 15, 2026

A Method to Study the Correlation Between Local Collagen Structure and Mechanical Properties of Atherosclerotic Plaque Fibrous Tissue
Published on: November 11, 2022
Endothelial dysfunction in plaque rupture and plaque erosion
Yuki Ishii1, Motoki Kure1, Hiroshi Kawasumi1
1Department of Cardiology, Showa Medical University Fujigaoka Hospital, 1-30 Fujigaoka, Aoba-ku, Yokohama, Kanagawa, 227-8501, Japan.
Insights
Vascular endothelial function, measured by flow-mediated dilation (FMD), was similarly impaired in acute coronary syndrome (ACS) patients with plaque erosion (PE) and plaque rupture (PR). However, FMD levels impacted major adverse cardiac events (MACE) differently based on the culprit lesion type.
Area of Science:
- Cardiology
- Vascular Biology
- Medical Imaging
Background:
- Vascular endothelial dysfunction is central to acute coronary syndrome (ACS) pathophysiology.
- Plaque erosion (PE) and plaque rupture (PR) are primary ACS mechanisms, but their differential impact on endothelial function remains unclear.
- Flow-mediated dilation (FMD) quantifies endothelial function.
Purpose of the Study:
- To compare endothelial function, assessed by FMD, between patients with PE and PR.
- To investigate the prognostic significance of FMD in relation to culprit lesion type in ACS.
Main Methods:
- Retrospective analysis of 160 ACS patients undergoing primary percutaneous coronary intervention (PCI).
- Optical frequency domain imaging (OFDI) categorized culprit plaques as PE or PR.
- FMD assessment was performed, and patients were stratified into high-FMD (>4.1%) and low-FMD (≤4.1%) groups.
- Clinical characteristics and major adverse cardiac events (MACE) were compared across four groups: PR-HighFMD, PR-LowFMD, PE-HighFMD, and PE-LowFMD.
Main Results:
- Endothelial function was similarly impaired in PE and PR groups (FMD 4.2% vs. 4.1%, P=0.85).
- The PR-HighFMD group exhibited the highest MACE-free survival.
- The PR-LowFMD group had the highest risk of MACE (HR=5.44, P=0.008), followed by PE-HighFMD and PE-LowFMD groups.
Conclusions:
- FMD is impaired in both PE and PR-related ACS.
- FMD has a prognostic impact on MACE in ACS patients, potentially varying with the type of culprit lesion.
- Further research is warranted to elucidate the prognostic role of endothelial function in different ACS etiologies.
Abstract:
Vascular endothelial function plays an important role in the pathophysiology of acute coronary syndrome (ACS). Plaque erosion (PE) and plaque rupture (PR) are the two major mechanisms of ACS; however, how the vascular endothelial function differs between these etiologies is not well understood. Flow-mediated dilation (FMD) is a method used to evaluate the endothelial function. We aimed to assess endothelial function using FMD in patients with PE and PR. ACS patients (N = 160) who underwent primary percutaneous coronary intervention (PCI) with optical frequency domain imaging (OFDI) and FMD assessment were retrospectively enrolled. Culprit plaques were categorized as PE or PR based on OFDI. Based on the median value of FMD (4.1%) in our data, patients were classified into high-FMD (> 4.1%) and low-FMD (≤ 4.1%) groups. Based on the plaque type and FMD values, the patients were divided into PR-HighFMD (N = 48), PR-LowFMD (N = 47), PE-HighFMD (N = 33), and PE-LowFMD (N = 32) groups, and then the clinical characteristics were compared. Major adverse cardiac events (MACE) were defined as cardiovascular death, nonfatal myocardial infarction, stroke, ischemia-driven revascularization, hospitalization for angina or heart failure. FMD was similarly impaired in the PE and PR groups (4.2% vs. 4.1%, P = 0.85). Most clinical characteristics did not differ between the groups. The PR-HighFMD group showed the highest MACE-free survival, followed by the PE-LowFMD (HR = 2.62, CI = 0.58-11.7, P = 0.21), PE-HighFMD (HR = 3.18, CI = 0.76-13.3, P = 0.11), and PR-LowFMD (HR = 5.44, CI = 1.55-19.1, P = 0.008) groups. FMD is likely to have a prognostic impact on patients with ACS, which might vary depending on the culprit lesion.
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