Iain P Bruce1, Hing-Chiu Chang2, Nan-Kuei Chen1,3, and Allen W Song1
1Brain Imaging and Analysis Center, Duke University Medical Center, Durham, NC, United States, 2Department of Diagnostic Radiology, University of Hong Kong, 3Biomedical Engineering, University of Arizona, Tuscan, AZ, United States
Synopsis
When diffusion MRI
data is acquired with 3D multi-slab and/or multi-shot imaging techniques, scan
times are often lengthy and phase variations between the acquired shots and/or
slice-encoding planes of 3D slabs introduce severe motion artifacts in slice images.
To accelerate the acquisition of high spatial resolution diffusion MRI volumes
with high SNR and fidelity, we outline a 3D image reconstruction model that simultaneously
accounts for both in-plane and through-plane motion artifacts in 3D multi-band,
multi-slab and multi-shot diffusion data. Diffusion data acquired and reconstructed
in this fashion can be acquired at sub-millimeter spatial resolution with high
SNR in ~1-2min.
Purpose:
Using
single-shot echo planar imaging (EPI) techniques, the spatial resolution of diffusion
MRI (dMRI) images is typically constrained by the SNR achievable within the
limited acquisition window (due to transverse relaxation time), and the need to
minimize motion artifacts and image distortions. With multi-shot EPI, on the
other hand, high-resolution dMRI can be reliably achieved through multiplexed sensitivity
encoding (MUSE)1,
where shot-to-shot phase variations that would otherwise deteriorate image
quality are corrected.
However, the SNR can be inherently low at very high resolutions. To achieve sufficient
SNR, 3D multi-slab imaging techniques can be employed. For single-shot 3D
acquisitions, bulk through-plane motion across a 3D slab can be accounted for by
using phase variations estimated from low resolution navigator images acquired at
kz=0 following the acquisition of
each slice encoding plane (kz-plane)
of a 3D slab2. In
multi-shot 3D acquisitions, however, the time separating the first shot in the
first kz-plane in a slab and the last
shot in the last kz-plane in the same
slab is proportional to TR·Nshots·Nkz, which can span 2-10min
for a single dMRI volume and introduce inaccuracy in phase estimation. Accelerating
multi-shot 3D acquisitions through multi-band imaging techniques, we present a
3D multi-band MUSE model (3D-MB-MUSE) in Fig. 1, in which Fourier encoded coil
sensitivity variations across the excited 3D slabs reconstruct all shots in all
kz-planes of a multi-band slab at
once, while simultaneously accounting for both in-plane and through-plane
motion artifacts across shots/kz-planes/bands.Methods:
Whole
brain in-vivo multi-band, multi-slab, and multi-shot dMRI data was acquired in
a commercial 3T GE MR750 scanner using a 32 channel head coil. Four interleaved
shots were used to image a 25.6cm FOV in a 256×256 acquisition matrix. Custom 3D
multi-band pulses simultaneously excited three 10mm slabs spaced 48mm apart. One
b=0 and three b=800s/mm2 dMRI volumes were acquired with six
multi-band slabs each. Slabs overlapped by 20% and were encoded with 12 kz-planes and 20% oversampling in z, resulting in a spatial resolution of
1.0mm3 with whole-brain coverage. To avoid T1 cross-talk artifacts,
odd slabs were acquired in their entirety within a volume before even slabs,
thereby enabling the SNR optimal 1.5sec TR for multi-slab imaging3. Under this
scheme, the overall acquisition time for each volume was 2min 24sec. In each
shot, bulk motion across kz was
corrected in the raw data using phase variations estimated from additional low-resolution
navigator images acquired at kz=0. Using
coil sensitivities derived from an additionally acquired 3D single-band b=0
volume, shot-to-shot and kz-to-kz phase variations were estimated in
each of the simultaneously excited slabs using a 3D adaptation of the SENSE4 model before being inserted into 3D-MB-MUSE. Finally, reconstructed slabs were
stitched together using slab profile encoding5, and brain extraction was performed using FSL6.Results and Discussion:
Fig.
2 presents a single diffusion-weighted multi-band multi-shot 3D slab
reconstructed with 3D-MB-MUSE. When a 1D-FFT converts the slice encoded multi-shot
aliased slab into aliased slab images, severe motion artifacts arise in the
phase encoding direction of each slice. By accounting for phase variations
across both shots and kz-planes in
the three aliased dMRI slabs, 3D-MB-MUSE reconstructs the aliased slice-encoded
slab into un-aliased slab images that are free of motion artifacts. While most
3D multi-slab models use coil sensitivities derived from a collapsed slab
(acquired at kz=0) to reconstruct all
slices in the slab, aliasing artifacts often arise in slices towards the outer
edges of thick slabs. Using Fourier encoded sensitivities that vary across the
slab, the resulting slab images in Fig. 2 exhibit minimal artifacts from either
reconstructing in-plane shots or separating through-plane bands. When stitched
together in Fig. 3, the b=0 and trace-weighted volumes exhibit high SNR in
1.0mm3 voxels with only minor slab banding artifacts, which may be further
reduced through additional signal-normalization steps in post-processing. Conclusion:
The
3D-MB-MUSE model in Fig. 1 presents an expandable framework that can account
for various artifacts associated with 3D multi-slab, multi-band, and multi-shot
diffusion imaging. In this abstract, both shot-to-shot and kz-to-kz
motion artifacts have been accounted for, and variable coil sensitivities
across a slab have been used to separate 3D multi-band slabs acquired with
multi-shot EPI. Building on this framework, current work includes accounting
for 3D imaging artifacts such as slab profile distortions and T1 cross-talk
between slabs, which will ultimately allow slabs to be interleaved within a
single 1.5sec TR. Reconstructing interleaved multi-shot and multi-band 3D slabs
with 3D-MB-MUSE would permit whole-brain volumes to be acquired at
sub-millimeter resolutions with sufficient SNR to produce reliable tractography
in ~1min, effectively enabling a widespread adoption of high-resolution dMRI.Acknowledgements
This work was supported in part by NIH grants NS-075017 and R24-106048.References
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