🤖 AI Summary
In diffusion MRI, microstructural parameters—such as axonal/cellular volume, size, and type—are severely confounded by fiber orientation and orientational dispersion. To address this, we propose Microstructural Propagator Imaging (MPI), a novel framework that directly models the probability density function of water molecule displacements at the microscopic scale. MPI introduces diffusion metrics fully decoupled from fiber orientation distributions and multi-fiber crossings, thereby eliminating dependence on macroscopic structural assumptions. The method integrates spherical harmonic-based regional modeling, multi-scale signal simulation, and a machine learning regression framework. Validation on both synthetic and real human brain data demonstrates that MPI-derived metrics exhibit clear biological interpretability, specifically reflecting alterations in microstructural integrity. Moreover, MPI significantly enhances sensitivity and specificity to tissue microstructural features compared to conventional approaches.
📝 Abstract
We propose Microscopic Propagator Imaging (MPI) as a novel method to retrieve the indices of the microscopic propagator which is the probability density function of water displacements due to diffusion within the nervous tissue microstructures. Unlike the Ensemble Average Propagator indices or the Diffusion Tensor Imaging metrics, MPI indices are independent from the mesoscopic organization of the tissue such as the presence of multiple axonal bundle directions and orientation dispersion. As a consequence, MPI indices are more specific to the volumes, sizes, and types of microstructures, like axons and cells, that are present in the tissue. Thus, changes in MPI indices can be more directly linked to alterations in the presence and integrity of microstructures themselves. The methodology behind MPI is rooted on zonal modeling of spherical harmonics, signal simulation, and machine learning regression, and is demonstrated on both synthetic and Human Diffusion MRI data.