Keywords: MR Fingerprinting, MR Fingerprinting
Motivation: Diffusion MRI can be corrupted by phase errors due to physiological motion, bulk motion, eddy currents, and other system imperfections, which makes its efficient embedding into MR Fingerprinting challenging.
Goal(s): To develop a new approach to correct artifacts in multidimensional MR Fingerprinting (mdMRF) for simultaneous relaxation and diffusion quantification, that obviates cardiac gating, motion compensation, navigators, or data removal.
Approach: Modeling potential phase errors using phase offset and phase dispersion during dictionary generation, then quantifying and correcting measured phase errors in dictionary matching.
Results: The proposed approach significantly mitigates artifacts in mdMRF diffusion parameter mapping.
Impact: Phase error-induced artifacts due to physiological motion, bulk motion, and eddy currents is a key limitation in diffusion MRI. We develop an approach to improve robustness and efficiency of artifact correction in multidimensional MR Fingerprinting for relaxation and diffusion mapping.
This work was supported by Siemens Healthineers, NIH grants R01 CA269604, R01 CA282516, R01 NS109439, UKRI MR/W031566.
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Figure 1. (A) mdMRF sequence consists of multiple segments, each staring with a preparation module, followed by data acquisition and ending with a wait time. (B) DP scheme used for diffusion encoding in mdMRF. (C) Phase offset and phase dispersion within a voxel are used to model the phase errors during diffusion preparation (before 90° tip-up pulse) for each diffusion-encoded segment. (D) Simulated mdMRF signal evolutions with and without phase errors. The phase errors cause signal attenuation and phase variation, with varying effects from phase offset and phase dispersion.
Figure 2. Reconstructed diffusion-weighted images that are affected by phase error effects including both magnitude (first row) and phase (second rows, unit: radians), the quantified phase offset maps (third row, unit: radians), and phase dispersion maps (fourth row, unit: radians) across all 6 diffusion encoding directions.
Figure 3. Comparison of ADC maps quantified using different methods. The ADC maps quantified without error removal or modeling suffer from severe shading artifacts (first row). By removing the corrupted segments, the artifacts can be significantly mitigated (second row). However, there are still some artifacts not removed, particularly around the ventricle anatomy (highlighted by red arrows). The proposed method can mitigate the artifacts more completely (third row). Color bar unit: 10-6 mm2/s.
Figure 4. T1, T2, FA and colored FA maps from the first healthy subject scan. Without phase error removal or modeling, the FA and colored FA maps are totally corrupted (first row). With the corrupted segments excluded, the maps can be significantly improved, but still suffers from some artifacts (second row, highlighted by red arrows). The proposed method yields best diffusion parameter mapping (third row). T1 and T2 color bar unit: ms.
Figure 5. T1, T2, FA and colored FA maps from the second healthy subject scan. Without phase error removal or modeling, the FA and colored FA maps are totally corrupted (first row). With the corrupted segments excluded, the maps can be significantly improved, but still suffers from some artifacts (second row, highlighted by red arrows). The proposed method yields best diffusion parameter mapping (third row).