To better understand how the underlying microstructure and pathology affect the DT-CMR signal in vivo, more realistic numerical models that account for irregular myocyte configurations such as sheetlets are necessary. We manually segmented cardiomyocytes from pig histology and confirmed that the resulting substrate is representative of the local microstructure through automatic segmentation of the surrounding tissue with a convolutional neural network. Monte Carlo random walk simulations, covering short and long mixing times and varying compartment diffusivities, show a mismatch between the results for the histology-based substrate and a simple cuboid model with comparable ECV and mean cell size.
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