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Baerentzen, J. A.

Publications and source records attributed to Baerentzen, J. A..

2 recordsLinked to original sources

PhyMorphS: A Physics-Guided Framework for Mesh-Based Morphological Synthesis of White Matter Microstructures

Numerical phantoms provide controlled 3D representations of brain tissue microstructure for developing and evaluating biophysical models of diffusion-weighted Magnetic Resonance Imaging (dMRI). Existing phantom synthesizers employ different geometric primitives and optimization strategies to generate densely packed substrates with diverse axonal morphologies. However, direct deformation of axonal surfaces under mechanical constraints remains less explored. We propose PhyMorphS, a mesh-based framework in which axonal morphology emerges through physics-guided growth and interactions with the local microstructural environment, without constraining cross-sections to predefined symmetric shapes. In PhyMorphS, axons, myelin sheaths, and cell bodies are represented by triangle meshes, while a mass-spring system and collision-resolution scheme guide iterative axonal growth under mechanical and packing constraints. This enables irregular, asymmetric, and non-convex cross-sections, longitudinal diameter variation, and user-defined morphological alterations such as axonal beading and myelin layer decompaction. We evaluate PhyMorphS against large-scale X-ray nano-holotomography segmentations of real 3D axons from four white matter regions with distinct fiber organizations. The synthesized axons reproduce key region-specific morphological characteristics and achieve high packing densities, while the parallelized implementation scales approximately linearly with axon count in the generation voxel. By reproducing the geometric variability observed in real WM tissue, PhyMorphS provides controlled substrates for investigating how realistic morphology influences simulated dMRI signals, testing the geometric assumptions of biophysical microstructure models, and generating diverse paired microstructure-signal datasets for training machine-learning models.

neuroscience↗

Exploring white matter dynamics and morphology through interactive numerical phantoms: The White Matter Generator

Brain white matter is a dynamic environment that continuously adapts and reorganizes in response to stimuli and pathological changes. Glial cells, especially, play a key role in tissue repair, inflammation modulation, and neural recovery. The movements of glial cells and changes in their concentrations can influence the surrounding axon morphology. We introduce the White Matter Generator (WMG) tool to enable the study of how axon morphology is influenced through such dynamical processes, and how this, in turn, influences the diffusion-weighted MRI signal. This is made possible by allowing interactive changes to the configuration of the phantom generation throughout the optimisation process. The phantoms can consist of axons, myelinated axons, and cell clusters, separated by extra-cellular space. Due to morphological flexibility and computational advantages during the optimisation, the tool uses ellipsoids as building blocks for all structures; chains of ellipsoids for axons, and individual ellipsoids for cell clusters. After optimisation, the ellipsoid representation can be converted to a mesh representation which can be employed in Monte-Carlo diffusion simulations. This offers an effective method for evaluating tissue microstructure models for diffusion-weighted MRI in controlled realistic white matter environments. Hence, the WMG offers valuable insights into white matters adaptive nature and implications for diffusion-weighted MRI microstructure models, and thereby holds the potential to advance clinical diagnosis, treatment, and rehabilitation strategies for various neurological disorders and injuries.

neuroscience↗