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Center for Computational and Digital Health Innovation

High-Fidelity Mechanistic-Probabilistic Models of Arterial Tissues

Advancing the field of probabilistic modeling and simulations, our research enables the integration of materials complexity in patient-specific simulation frameworks, accounting for inter- and intra-patient variability.

Lead PI:

  • Johann Guilleminot

Center Researchers:

    Related Publications

    • Spatially-dependent material uncertainties in anisotropic nonlinear elasticity: Stochastic modeling, identification, and propagation
    • A random field model for anisotropic strain energy functions and its application for uncertainty quantification in vascular mechanics
    • Stochastic hyperelastic constitutive laws and identification procedure for soft biological tissues with intrinsic variability
    • Stochastic modeling of the Ogden class of stored energy functions for hyperelastic materials: the compressible case
    • Stochastic modeling of a class of stored energy functions for incompressible hyperelastic materials with uncertainties

    In the News:

      The Challenge

      Cardiovascular modeling and simulations require developing computational/mathematical models capturing the mechanistic behavior of arterial walls. While many constitutive models have been developed to represent the response of these tissues at various scales, the proper integration of inter- and intra-patient variability remains an open problem.

      Neglecting response variability can lead to poor accuracy in predictions, with important consequences in terms of diagnostic and treatment.

      To support the advancement of so-called digital twin frameworks, which typically involve a patient-specific replicate of the arterial geometry but do not account for intrinsic stochasticity in the system, there is a need to develop new computational methods and high-fidelity models capturing the variability in the mechanistic response of soft tissues.

      Developing these models challenges the current the state of the art in computational mechanics, due to the variety of constraints that they must satisfy to ensure that predictions can be computed, as well as lack of results regarding the simulation of stochastic fields on complex domains.

      Our Solution

      The Guilleminot Lab has developed a series of high-fidelity probabilistic models that enable the integration of geometrical complexity and material stochasticity in near real time.

      Leveraging recent results on numerical implicit representations for Gaussian fields, we provide a framework decoupling geometrical features and admissibility constraints for material parameters. The former are integrated on the fly, using ad hoc algorithms that can automatically process MRI inputs. The latter are introduced into an information-theoretical paradigm, which allows us to reduce bias in predictions.

      We have shown, through thorough validation analyses, that the proposed framework can capture stochasticity in the response of human arterial layers, with and without spatial dependencies.

      This work bridges the gap between the consideration of patient-specific geometrical models and the integration of material stochasticity, ultimately enhancing the accuracy and robustness of cardiovascular simulations in digital twin frameworks.

      Simulation of stochastic material parameters on patient-specific geometries
      Simulation of stochastic material parameters on patient-specific geometries
      Simulation of the mechanical response (stress) in the arterial wall; red regions indicate higher variability
      Simulation of the mechanical response (stress) in the arterial wall; red regions indicate higher variability
      Our model can reproduce observed intra-patient variability in the mechanical response of the media layer; black lines represent human samples, blue line is the mean, and red lines represent the confidence interval from the model
      Our model can reproduce observed intra-patient variability in the mechanical response of the media layer; black lines represent human samples, blue line is the mean, and red lines represent the confidence interval from the model

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