Keywords: Diffusion Reconstruction, Relaxometry
Motivation: The subspace-based reconstruction is an SNR-efficient approach for distortion-free diffusion-relaxometry MRI with highly under-sampled echo-planar time-resolved acquisition (EPTI), in which the needed bases can be estimated from simulations. However, the simulations may not be able to fully capture the signal evolution in complex human tissue.
Goal(s): To improve the subspace-based EPTI reconstruction by estimating the bases from acquired calibration data.
Approach: The efficacy of the new data-driven subspace reconstruction was evaluated with in vivo EPTI experiments.
Results: High-resolution, under-sampled EPTI images are reliably reconstructed using the data-driven subspace reconstruction.
Impact: Our study presents a new data-driven approach for estimating the bases for the subspace-based echo-planar time-resolved imaging (EPTI) reconstruction, which may better reflect the underlying microstructure than the numerical simulation and further facilitate studies with diffusion-relaxometry MRI.
We thank the funding support from GE Healthcare, NIH R01NS095985, and NIH K99AG080076.
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Figure 1. (A) The sampling trajectory of the fully sampled low-resolution calibration scan. A navigator is acquired at the end of the readout (in gray). The phase encoding polarity of the navigator is dependent on the ky location of the last image-echo. (B) The sampling trajectory and (C) sequence of the under-sampled high-resolution EPTI scan. The sampling is denser at ky~0 for the inter-shot phase correction and subspace reconstruction. TESE is marked in (B) and (C). Table 1. Detailed scan parameters.
Figure 2. (A-C) The pipeline of estimating subspace bases from the acquired calibration data. (D-F) Subspace reconstruction of high-resolution EPTI images with the estimated bases from the calibration scan.
Figure 3. Reconstruction results of Experiment 1, including (A-C) The mean images of b=0, 1, and 2 ms/μm2 (only averaged over different b=0s or diffusion encoding directions. No average along the TE dimension), at the shortest (TE=50 ms) and longest TEs (TE=103 ms), and the fitted T2* maps.
Figure 4. Results of Experiment 1, including (A) the directionally-encoded color (DEC) maps and the line representation of the (B) principal and (C) secondary fiber orientations in a selected ROI (red box) in 7 different TE groups. The red arrowheads note the observed consistent and gradual changes in the secondary fiber orientation over different TEs in two example pixels, potentially indicating changing sensitivity to tissue components with different T2*.
Figure 5. Subspace reconstruction results of Experiment 2 with Nm=4 magnitude bases estimated from (A) the calibration scan of the same subject (Basissame); (B) the calibration scan of a different subject (Basisdifferent); (C) the calibration scans of (A) and (B) together (Basiscombine), and (D) a simulation with varying T2 and T2* (Basissimul). Example single-direction diffusion-weighted images, FA maps, and the differences (intensity ×5) between (B-D) and (A) are shown.