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Thomas Lavigne

Publications and source records attributed to Thomas Lavigne.

5 recordsLinked to original sources

Open-source MRI-informed computational model of human cortical folding

The human cerebral cortex, initially smooth, progressively folds during fetal brain development in utero, giving rise to cortical convolutions. Atypical cortical folding patterns can be associated with neurodevelopmental and neurological disorders. To better understand these conditions, it is crucial to first examine the factors governing healthy cortical folding. Computational modeling provides a powerful way for this purpose and has already helped understanding the influence of key biomechanical parameters on the folding pattern. However, most existing models use simplified geometries, limiting calibration and validation with fetal and neonatal brain Magnetic Resonance Imaging (MRI) and neglecting the influence of initial geometry on fold development. On the other hand, simulations on realistic brain geometries introduce additional challenges, including collision handling, fold characterization, and additional computational cost. Furthermore, model parameters are often difficult to interpret, complicating comparison, clinical translation, and calibration. Finally, computational models of cortical folding also remain rarely accessible. In this work, we introduce a novel computational model of cortical folding, developed using the open-source code FEniCS to simulate folding on a whole-brain geometry generated from fetal MRI data. We also propose a modular, interpretable, and scalable simulation framework built around this computational model and openly available to the community. It uses fetal MRI data to generate realistic input brain meshes and estimate key biomechanical parameters such as cortical growth rate. The framework also integrates a spectral metric for cortical surface analysis to optimize folding pattern predictions from an healthy fetal MRI dataset.

physics.bio-ph

Hierarchical poromechanical approach to investigate the impact of mechanical loading on human skin micro-circulation

Research on human skin anatomy reveals its complex multi-scale, multi-phase nature, with up to 70% of its composition being bounded and free water. Fluid movement plays a key role in the skin's mechanical and biological responses, influencing its time-dependent behavior and nutrient transport. Poroelastic modeling is a promising approach for studying skin dynamics across scales by integrating multi-physics processes. This paper introduces a hierarchical two-compartment model capturing fluid distribution in the interstitium and micro-circulation. A theoretical framework is developed with a biphasic interstitium -- distinguishing interstitial fluid and non-structural cells -- and analyzed through a one-dimensional consolidation test of a column. This biphasic approach allows separate modeling of cell and fluid motion, considering their differing characteristic times. An appendix discusses extending the model to include biological exchanges like oxygen transport. Preliminary results indicate that cell viscosity introduces a second characteristic time, and at high viscosity and short time scales, cells behave similarly to solids. A simplified model was used to replicate an experimental campaign on short time scales. Local pressure (up to 31 kPa) was applied to dorsal finger skin using a laser Doppler probe PF801 (Perimed Sweden), following a setup described in Fromy Brain Res (1998). The model qualitatively captured ischemia and post-occlusive reactive hyperemia, aligning with experimental data. All numerical simulations used the open-source software FEniCSx v0.9.0. To ensure transparency and reproducibility, anonymized experimental data and finite element codes are publicly available on GitHub.

q-bio.TO

Synthetic Porous Microstructures: Automatic Design, Simulation, and Permeability Analysis

This study introduces an open-source computational framework for the generation and permeability evaluation of synthetic porous media. The proposed methodology integrates crystallographic and meshing tools to construct controlled microstructures with tunable porosity, facilitating seamless transitions from geometric modelling to computational domains for numerical simulations. The generated structures are analysed through fluid-structure interaction (FSI) simulations, leveraging the Entropically Damped Artificial Compressibility (EDAC) formulation in conjunction with the Discretization-Corrected Particle Strength Exchange (DC-PSE) method. A novel approach for the numerical estimation of the macroscopic permeability tensor is presented, employing a stochastic upscaling technique inspired by the volume averaging method. To validate the framework, we investigate the transition between creeping and non-Darcy flow regimes through parametric permeability studies, utilizing a one-dimensional approach for practical benchmarking. The results establish a foundation for experimental validation and provide insights into the customised design of porous structures for engineering and biomedical applications, offering a versatile tool for research in fluid transport and porous media mechanics.

q-bio.TO

Poromechanical modelling of the time-dependent response of in vivo human skin during extension

This paper proposes a proof of concept application of a biphasic constitutive model to identify the mechanical properties of in vivo human skin under extension. Although poromechanics theory has been extensively used to model other soft biological tissues, only a few studies have been published for skin, and most have been limited to ex vivo or in silico conditions. However, in vivo procedures are crucial to determine the subject-specific properties at different body sites. This study focuses on cyclic uni-axial extension of the upper arm skin, using unpublished data collected by Chambert et al. Our analysis shows that a two-layer finite element model allows representing all relevant features of the observed mechanical response to the imposed external loading, which was composed, in this contribution, of four loading-sustaining-unloading cycles. The Root Mean Square Error (RMSE) between the calibrated model and the measured Force-time response was 8.84e-3 N. Our biphasic model represents a preliminary step toward investigating the mechanical conditions responsible for the onset of injury. It allows for the analysis of changes in Interstitial Fluid (IF) pressure, flow, and osmotic pressure, in addition to the mechanical fields. Future work will focus on the interaction of multiple biochemical factors and the complex network of regulatory signals.

q-bio.TO

Multi-compartment poroelastic models of perfused biological soft tissues: implementation in FEniCSx

Soft biological tissues demonstrate strong time-dependent and strain-rate mechanical behavior, arising from their intrinsic visco-elasticity and fluid-solid interactions (especially at sufficiently large time scales). The time-dependent mechanical properties of soft tissues influence their physiological functions and are linked to several pathological processes. Poro-elastic modeling represents a promising approach because it allows the integration of multiscale/multiphysics data to probe biologically relevant phenomena at a smaller scale and embeds the relevant mechanisms at the larger scale. The implementation of multi-phasic flow poro-elastic models however is a complex undertaking, requiring extensive knowledge. The open-source software FEniCSx Project provides a novel tool for the automated solution of partial differential equations by the finite element method. This paper aims to provide the required tools to model the mixed formulation of poro-elasticity, from the theory to the implementation, within FEniCSx. Several benchmark cases are studied. A column under confined compression conditions is compared to the Terzaghi analytical solution, using the L2-norm. An implementation of poro-hyper-elasticity is proposed. A bi-compartment column is compared to previously published results (Cast3m implementation). For all cases, accurate results are obtained in terms of a normalized Root Mean Square Error (RMSE). Furthermore, the FEniCSx computation is found three times faster than the legacy FEniCS one. The benefits of parallel computation are also highlighted.

q-bio.TO