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Dynamic elastography, whether based on magnetic resonance, ultrasound, or optical modalities, attempts to reconstruct quantitative maps of the viscoelastic properties of biological tissue, properties that are altered by disease and injury, by noninvasively measuring mechanical wave motion in the tissue. Most reconstruction strategies that have been developed neglect boundary conditions, including quasistatic tensile or compressive loading resulting in a nonzero prestress. Significant prestress is inherent to the functional role of some biological tissues currently being studied using elastography, such as skeletal and cardiac muscle, arterial walls, and the cornea. In the present article, we review how prestress alters both bulk mechanical wave motion and wave motion in one- and two-dimensional waveguides. Key findings are linked to studies on skeletal muscle and the human cornea, as one- and two-dimensional waveguide examples. This study highlights the underappreciated combined acoustoelastic and waveguide challenge to elastography. Can elastography truly determine viscoelastic properties of a material when what it is measuring is affected by both these material properties and unknown prestress and other boundary conditions?
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Towards linking histological changes to liver viscoelasticity: a hybrid analytical-computational micromechanics approach
Abstract Motivated by elastography that utilizes tissue mechanical properties as biomarkers for liver disease, with the eventual objective of quantitatively linking histopathology and bulk mechanical properties, we develop a micromechanical modeling approach to capture the effects of fat and collagen deposition in the liver. Specifically, we utilize computational homogenization to convert the microstructural changes in hepatic lobule to the effective viscoelastic modulus of the liver tissue, i.e., predict the bulk material properties by analyzing the deformation of repeating unit cell. The lipid and collagen deposition is simulated with the help of ad hoc algorithms informed by histological observations. Collagen deposition is directly included in the computational model, while composite material theory is used to convert fat content to the microscopic mechanical properties, which in turn is included in the computational model. The results illustrate the model’s ability to capture the effect of both fat and collagen deposition on the viscoelastic moduli and represents a step towards linking histopathological changes in the liver to its bulk mechanical properties, which can eventually provide insights for accurate diagnosis with elastography.
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- Award ID(s):
- 2111234
- PAR ID:
- 10566512
- Publisher / Repository:
- IOP Publishing
- Date Published:
- Journal Name:
- Physics in Medicine & Biology
- ISSN:
- 0031-9155
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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