Key result
Atherosclerotic lesion structure and composition strongly influence aortic wall stress and strain energy.
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An experimental technique was developed to determine the finite strain field in heterogeneous, diseased human aortic cross sections at physiologic pressures in vitro. Also, the distributions within the cross sections of four histologic features (disease-free zones, lipid accumulations, fibrous intimal tissue, and regions of calcification) were quantified using light microscopic morphometry. A model incorporating heterogeneous, plane stress finite elements coupled the experimental and histologic data. Tissue constituent mechanical properties were determined through an optimization strategy, and the distributions of stress and strain energy in the diseased vascular wall were calculated. Results show that the constituents of atherosclerotic lesions exhibit large differences in their bilinear mechanical properties. The distributions of stress and strain energy in the diseased vascular wall are strongly influenced by both lesion structure and composition. These results suggest that accounting for heterogeneities in the mechanical analysis of atherosclerotic arterial tissue is critical to establishing links between lesion morphology and the susceptibility of plaque to mechanical disruption in vivo.
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Beattie et al. (1998) studied Atherosclerosis of the human aorta. In vitro finite element and light microscopic morphometric mechanical analysis vs. Disease-free zones vs. lipid accumulations, fibrous intimal tissue, and calcification was evaluated on Distributions of stress and strain energy and constituent bilinear mechanical properties in the diseased vascular wall. Finite element analysis of 4 histologic features in atherosclerotic human aortas showed lesion structure and composition strongly influence vascular wall stress and strain energy.
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