The applicability of SQUASHER to EPI, along with a kz-dependent reconstruction approach for highly-accelerated 3D segmented EPI in dMRI
SQUASHER 3D-EPI: A 3D-EPI acquisition with slice and phase-encoding segmentation using frequency swept pulses for excitation and refocusing(4) was implemented to image thin slabs of less than 10 slices. A single navigator was used across all segments. Diffusion weighting was achieved using the spoiler gradients. Fast imaging by sub-sampling in the kz direction was evaluated with retrospective undersampling.
Reconstruction: Navigator correction was performed with linear phase-difference estimated from the navigator, and applied channel-specific. To evaluate the robustness of sub-sampling in kz direction, both a conventional 3D-GRAPPA algorithm5 and a kz-dependent 3D-GRAPPA algorithm(7) were implemented. The latter builds on an earlier modified GRAPPA approach(6), and utilizes a region-specific 3D kernel for different slice encoding locations.
Phantom imaging, A single-shot partition segmented diffusion weighted SE-EPI with TE/TR=143/4000ms, 1.5mm3 isotropic resolution, 8 slices/slab, 25% slab oversampling was used. This was used to compare the spectrum of the SQUASHER 3D-EPI against a standard implementation with a SINC RF-pulse. The SQUASHER data was retrospectively sub-sampled at rate 4×2 (ky × kz), and reconstructed using single-kernel and kz-dependent 3D-GRAPPA approaches.
In-vivo imaging was performed on a 3T Prisma, equipped with a 32 channel receiver coil. For GRAPPA kernel estimation, an ACS reference scan with 1 segment in the phase-encoding direction was acquired with TE/TR=129/800ms, 1.5x1.5x1mm3 resolution, 8 slices/slab, 25% slab oversampling, matrix size=128x128x10 and matched RF to the accelerated acquisition. For accelerated acquisitions, phase-encoding segmentation (two) was used, with TE/TR=91/800ms, FOV and resolution matching the reference scan. These acquisitions were repeated both with and without diffusion weighting.
Fig. 1 shows the signal energy of the acquisitions using SQUASHER and SINC encoding pulses, in the x-y-kz plane following a root-sum-squares combination across coils. SINC encoding exhibits a fast decay in energy in the kz direction, which hinders segmentation due to the low SNR in the high-frequency components. On the other hand, SQUASHER exhibits a slow decay in the kz direction, which may be favorable for slice segmentation correction.
Fig. 2 depicts a phantom reconstruction with 4×2 undersampling. Single-kernel reconstruction (b) suffers from residual aliasing and signal variation, whereas the kz-dependent kernels (b) enable a distortion-free image at this high acceleration rate. The signal variation in a reformatted view (d) shows the superiority of the kz-dependent kernels in maintaining the signal variations across slices in this thin slab.
Fig. 3 shows the application of these techniques to human brain imaging for a single slice from a 3D acquisition at 4-fold ky acceleration, with 2 different diffusion weightings, and with 1mm through plane resolution and 1.5x1.5mm in-plane resolution.
The use of SQUASHER and the kz-dependent GRAPPA algorithm allows for a higher SNR acquisition and better reconstruction. These provide a flexible, scalable approach for high resolution imaging with 3D-acquisitions of thin slabs.
For 3D thin-slab high resolution imaging, one of the challenges for the slice-segmentation is that the acquired kz slices have low signal. The low signal was previously addressed with the gSLIDER technique (4) where a Hadamard type encoding with n different RF pulses was used with n slices having coherent RF phase for increased signal. In contrast, SQUASHER requires a single RF encoding shape, while maintaining the conventional Fourier slice and phase encoding, but instead modifies the properties of the k-space signal for better segmentation.
In this study, we have shown the feasibility of combining SQUASHER and the kz-dependent GRAPPA for accelerated 3D EPI diffusion weighted imaging. Higher-resolution acquisitions and combination with SMS will be explored in future studies for faster whole brain coverage.
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