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Transl Res ; 240: 33-49, 2022 02.
Article in English | MEDLINE | ID: mdl-34478893

ABSTRACT

Identification of patients with high-risk asymptomatic atherosclerotic plaques remains an elusive but essential step in preventing stroke. However, there is a lack of animal model that provides a reproducible method to predict where, when and what types of plaque formation, which fulfils the American Heart Association (AHA) histological classification of human plaques. We have developed a predictive mouse model that reflects different stages of human plaques in a single carotid artery by means of shear-stress modifying cuff. Validated with over 30000 histological sections, the model generates a specific pattern of plaques with different risk levels along the same artery depending on their position relative to the cuff. The further upstream of the cuff-implanted artery, the lower the magnitude of shear stress, the more unstable the plaques of higher grade according to AHA classification; with characteristics including greater degree of vascular remodeling, plaque size, plaque vulnerability and inflammation, resulting in higher risk plaques. By weeks 20 and 30, this model achieved 80% and near 100% accuracy respectively, in predicting precisely where, when and what stages/AHA types of plaques develop along the same carotid artery. This model can generate clinically-relevant plaques with varying phenotypes fulfilling AHA classification and risk levels, in specific locations of the single artery with near 100% accuracy of prediction. The model offers a promising tool for development of diagnostic tools to target high-risk plaques, increasing accuracy in predicting which individual patients may require surgical intervention to prevent stroke, paving the way for personalized management of carotid atherosclerotic disease.


Subject(s)
Carotid Arteries/pathology , Plaque, Atherosclerotic/pathology , Animals , Apolipoproteins E/deficiency , Apolipoproteins E/metabolism , Biomarkers/metabolism , Carotid Arteries/physiopathology , Collagen/metabolism , Disease Models, Animal , Disease Progression , Humans , Inflammation/complications , Inflammation/pathology , Lipids/chemistry , Mice, Knockout , Myocytes, Smooth Muscle/metabolism , Plaque, Atherosclerotic/complications , Plaque, Atherosclerotic/physiopathology , Plaque, Atherosclerotic/prevention & control , Shear Strength , Stress, Mechanical , Translational Research, Biomedical , Vascular Remodeling
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