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Published on: November 19, 2020
An in vivo parameter identification method for arteries: numerical validation for the human abdominal aorta
Jan-Lucas Gade1, Jonas Stålhand1, Carl-Johan Thore1
1a Solid Mechanics, Department of Management and Engineering, Faculty of Science & Engineering , Linköping University , Linköping , Sweden.
This study introduces a new method to determine arterial mechanical properties in vivo using pressure-radius data. The technique accurately identifies properties in healthy aortas and detects diseased ones.
Area of Science:
- Biomedical Engineering
- Computational Mechanics
- Cardiovascular Research
Background:
- Accurate characterization of arterial mechanical properties is crucial for understanding cardiovascular health and disease.
- In vivo assessment of arterial biomechanics presents significant challenges due to complex physiological conditions.
Purpose of the Study:
- To propose and numerically validate a novel method for identifying in vivo mechanical properties of arterial tissue.
- To assess the method's accuracy for healthy and pathological human abdominal aortas.
Main Methods:
- Development of a parameter identification method using pressure-radius data.
- Numerical validation using 22 finite element models of the human abdominal aorta with known properties.
- Generation of synthetic pressure-radius data from in silico experiments for method testing.
Main Results:
- The method accurately identified material constants for elastin and stress-free radius in healthy abdominal aortas.
- Slight discrepancies were observed for collagen-related constants and axial prestretch in healthy models.
- The method successfully distinguished pathological aortas, though parameter identification showed larger errors in diseased cases.
Conclusions:
- The proposed parameter identification method is quantitatively validated for in vivo arterial mechanical property assessment.
- The method demonstrates potential for diagnosing healthy versus pathological abdominal aortas using clinical data.
- Further refinement may improve accuracy for collagen properties and axial prestretch in clinical applications.
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