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Novel insights into in‐vivo diffusion tensor cardiovascular magnetic resonance using computational modelling and a histology‐based virtual microstructure
Author(s) -
Rose Jan N.,
NiellesVallespin Sonia,
Ferreira Pedro F.,
Firmin David N.,
Scott Andrew D.,
Doorly Denis J.
Publication year - 2019
Publication title -
magnetic resonance in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.696
H-Index - 225
eISSN - 1522-2594
pISSN - 0740-3194
DOI - 10.1002/mrm.27561
Subject(s) - diffusion mri , nuclear magnetic resonance , thermal diffusivity , magnetic resonance imaging , diffusion , voxel , anisotropy , spin echo , fractional anisotropy , chemistry , sensitivity (control systems) , materials science , biomedical engineering , physics , computer science , optics , artificial intelligence , medicine , radiology , quantum mechanics , thermodynamics , electronic engineering , engineering
Purpose To develop histology‐informed simulations of diffusion tensor cardiovascular magnetic resonance (DT‐CMR) for typical in‐vivo pulse sequences and determine their sensitivity to changes in extra‐cellular space (ECS) and other microstructural parameters. Methods We synthesised the DT‐CMR signal from Monte Carlo random walk simulations. The virtual tissue was based on porcine histology. The cells were thickened and then shrunk to modify ECS. We also created idealised geometries using cuboids in regular arrangement, matching the extra‐cellular volume fraction (ECV) of 16–40%. The simulated voxel size was 2.8 × 2.8 × 8.0 mm 3 for pulse sequences covering short and long diffusion times: Stejskal–Tanner pulsed‐gradient spin echo, second‐order motion‐compensated spin echo, and stimulated echo acquisition mode (STEAM), with clinically available gradient strengths. Results The primary diffusion tensor eigenvalue increases linearly with ECV at a similar rate for all simulated geometries. Mean diffusivity (MD) varies linearly, too, but is higher for the substrates with more uniformly distributed ECS. Fractional anisotropy (FA) for the histology‐based geometry is higher than the idealised geometry with low sensitivity to ECV, except for the long mixing time of the STEAM sequence. Varying the intra‐cellular diffusivity ( D IC ) results in large changes of MD and FA. Varying extra‐cellular diffusivity or using stronger gradients has minor effects on FA. Uncertainties of the primary eigenvector orientation are reduced using STEAM. Conclusions We found that the distribution of ECS has a measurable impact on DT‐CMR parameters. The observed sensitivity of MD and FA to ECV and D IC has potentially interesting applications for interpreting in‐vivo DT‐CMR parameters.