A kz-dependent shift-variant 3D GRAPPA approach for reconstructing 2D under-sampled k-space is proposed. The method results in equal or lower g-factors compared to a conventional shift-invariant 3D kernel. In turn, this permits higher 2D ky-kz accelerations, and promises significant advantages for functional and diffusion imaging. The method is demonstrated with anatomical and diffusion imaging using thin slabs.
Several methods for better k-space interpolation have been proposed for GRAPPA, leading to improved performance. These include various regularization approaches3-5, different calibration approaches6-9, and extension of the initial GRAPPA system10-12. Recently, analysis of GRAPPA via Reproducing Kernel Hilbert Spaces suggests the conventional linear shift-invariant GRAPPA kernels may be sub-optimal13. While GRAPPA kernels have been extensively studied and analyzed for 2D imaging14,15, their design and optimization have not been thoroughly studied for the 3D case.
In this work, we propose an estimation procedure that depends on the slice encoding (kz) location for generating multiple 3D GRAPPA kernels for reconstructing different parts of volumetric k-space. We compare its performance to the standard 3D GRAPPA kernel approach15 in terms of image quality, noise amplification, and stability across dynamic images and under challenging conditions including thin slabs with limited coil sensitivity variations. We use anatomical imaging with undersampling along both the phase and slice-encoding and we use dMRI with 2X undersampling along the slice-encoding direction. For dMRI we use SQUASHER encoding with SE-EPI for generating a quadratic phase across the slab16.
kz -GRAPPA: The proposed reconstruction utilizes region-specific 3D kernels in the slice encoding direction. In order to estimate the missing k-space points ($$$k_{z}^{miss} $$$) from the measured data ($$$k_{z'}^{meas} $$$), at the slice encoding location $$$z \neq z'$$$ , a unique kernel with elements, $$$w_{nj}^{k_z} $$$, of size 3×4×2 (nRO×nPE×nPE2) across all coils is utilized to reconstruct the data in coil j. The kernels are calibrated using kx (readout) and ky (phase-encoding) points and with the choice of kernel the closest $$$k_{z'}^{meas} $$$ to $$$k_{z}^{miss} $$$ in the matched ACS data. The undersampling in ky is treated in a shift-invariant manner and for a given kz location only one kernel is generated for the kx – ky directions. The corresponding reconstruction equations is shown in Figure 1A, and a schematic illustration of kz-GRAPPA is in Figure 1C.
3D GRAPPA: For comparison, a shift-invariant 3D GRAPPA algorithm was implemented14,15, with a 3×4×4 kernel size. The kernel was calibrated across all available ACS data and all coils. The corresponding reconstruction equation is depicted in Figure 1, where Ry and Rz are the reduction factors in ky (phase-encoding) and kz (partition encoding), respectively, following the original convolution-based notation2.
Imaging: Data was acquired on a 3T Siemens Prisma scanner with a 32-channel head coil. In-vivo and Phantom GRE : Fully-sampled k-space using a 5120µs sinc RF pulse with a time bandwidth product of 4 and sequence parameters: TE/TR/FA= 30/35ms/15°, resolution=1.3×1.3×1.3 mm3. In-vivo: FOV=330×225×50 mm3, 46.7%OS . phantom: FOV=332×332×20.8 mm3 25%OS.
DWI Multislab SE-EPI with SQUASHER17 Encoding: Excitation/Refocusing = HS2R12/HS2R14, duration 7680µs, 1mm3, TE/TR of 92.2/1610ms with 12slices/slab, 10 slabs, FOV 210x210x120 mm3, iPAT=2, Volume acquisition time (VAT)=26s. Diffusion data were acquired across 2shells (b=1500 and b=3000 s/mm2) using different diffusion encoding vectors $$$\vec{b}$$$. Each kz plane (from a single-shot acquisition) is corrected first for in-plane undersampling and for physiological induced phase-variation from the diffusion sensitizing gradient. 3D GRAPPA and kz-GRAPPA kernels are calculated from a b=0 ACS acquisition and applied to undersampling along kz, where no data has been acquired for alternating kz planes, ie all even kz planes.
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