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Updated: Jan 19, 2026

Quantitative Analysis and Characterization of Atherosclerotic Lesions in the Murine Aortic Sinus
Published on: December 7, 2013
Coronary atherosclerotic plaque composition and classification in hypercholesterolemic pigs
Mingqiao Li1, Di Tian2, Patrice Delafontaine1
1Tulane University School of Medicine, Department of Medicine, New Orleans, LA, 70112, USA.
Familial hypercholesterolemia pigs fed a high-fat diet develop coronary atherosclerosis similar to humans. This study establishes a classification system for porcine coronary plaques, aiding cardiovascular disease research.
Area of Science:
- Cardiovascular Research
- Translational Medicine
- Animal Models
Background:
- Familial hypercholesterolemia (FH) pigs on a high-fat diet develop coronary atherosclerosis mimicking human disease.
- FH pigs are valuable pre-clinical models for atherosclerosis research.
- A standardized classification system for porcine coronary atherosclerosis is lacking.
Purpose of the Study:
- To develop and validate a classification system for coronary atherosclerotic plaques in FH pigs.
- To correlate porcine plaque characteristics with human coronary atherosclerotic lesion types.
Main Methods:
- Quantified morphological features of 104 coronary plaque fragments from FH pigs.
- Employed K-means clustering to categorize plaques based on morphology and cellular composition.
- Assessed plaque neovascularization, collagen, apoptosis, and calcification for classification.
Main Results:
- Identified 4 distinct coronary plaque groups (A-D) in FH pigs using unsupervised clustering.
- Classified group A as pre-atheroma and groups C-D as advanced atheroma.
- Correlated porcine plaque groups A, B, C, and D with human lesion types III, IV, V, and VI, respectively.
Conclusions:
- FH pigs serve as a suitable pre-clinical model for human-like coronary atherosclerosis.
- The established classification system enhances the utility of FH pigs for coronary artery disease (CAD) research.
- This model shows significant potential for studying vulnerable plaque and advancing CAD discovery research.
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