We propose to sparsely sample in vivo cardiac diffusion tensor imaging (CDTI) by combining a phase-corrected low-rank model and sparsity constraint. The proposed method was evaluated on 7 hypertrophic cardiomyopathy patients. Helix angle and mean diffusivity maps were compared against employing single constraint, and changes in helix angle transmurality and mean diffusivity were evaluated using Wilcoxon signed rank test to statistically determine the highest achievable acceleration factors preserving CDTI measurements with no significant difference. Our framework shows promise in accelerating acquisition window while preserving myofiber architecture features, and may allow higher spatial resolution or shorter temporal footprint in the future.
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