Philip Kenneth Lee1, Xuetong Zhou1,2, Nan Wang1, and Brian Andrew Hargreaves1,2,3
1Radiology, Stanford University, Stanford, CA, United States, 2Bioengineering, Stanford University, Stanford, CA, United States, 3Electrical Engineering, Stanford University, Stanford, CA, United States
Synopsis
Keywords: Pulse Sequence Design, Diffusion/other diffusion imaging techniques, abdomen, free-breathing
Abdominal imaging is frequently performed with uncomfortable
breath holds, or respiratory triggering to reduce the effects of respiratory
motion. Diffusion weighted sequences provide a useful clinical contrast but
have prolonged scan times due to low SNR. These scans cannot be reliably completed in a
single breath hold, and respiratory triggering has low scan efficiency.
We present a respiratory resolved, diffusion-prepared 3D
sequence that obtains distortionless diffusion weighted images during free-breathing.
We describe techniques to address the myriad of challenges including: 3D
shot-to-shot phase correction, respiratory binning, diffusion encoding during
free-breathing, and robustness to off-resonance.
Introduction
Diffusion weighted imaging (DWI) is a desirable clinical
contrast for treatment planning and cancer screening. Abdominal DWI is a
challenge due to respiratory motion, long scan times, and off-resonance, which
causes distortion in the widely used DW-EPI sequence. Respiratory triggering
can reduce respiratory motion artifacts, but this is ineffective for irregular
breathing patterns and depends on correct placement of the bellows. Breath-holds are not feasible for all patients.
We present a tightly integrated sequence and
reconstruction that obtains distortionless diffusion images under
free-breathing. We describe techniques to address the myriad of challenges including:
3D shot-to-shot phase correction, respiratory binning, diffusion encoding during
free-breathing, and robustness to off-resonance.Methods
Sampling trajectory: Non-Cartesian
trajectories are commonly employed in abdomen imaging due to their robustness
to motion artifacts. However, the sampling density of non-Cartesian
trajectories is difficult to control near the k-space center. This poses a
challenge for obtaining low-resolution 3D phase navigators required to correct varying
phase from motion-sensitizing diffusion gradients. A Cartesian trajectory
allows the sampling density and phase navigator resolution to be easily
adjusted. The ky-kz trajectory for each shot has two stages. The
first stage randomly samples inner k-space. These lines are
reconstructed using parallel imaging and used for phase correction in a
self-phase-navigated strategy1. The second stage samples outer k-space
following a Variable Density Radial (VD-RAD) Cartesian ordering2.
Cartesian sampling makes reconstruction tractable due
to separability along the readout dimension. Naively storing zero-filled
k-space with matrix size 256$$$\,×\,$$$256$$$\,×\,$$$32$$$\,×\,$$$24 coils$$$\,×\,$$$100 shots requires ~40GB of RAM.
Image encoding$$$\,$$$/$$$\,$$$diffusion contrast:
A twice-refocused, M1-nulled diffusion preparation was paired with
Cartesian 3D RF-spoiled gradient echo (FLASH) for distortionless imaging. A stabilizer gradient
along the slice direction before the tipup stores the same net magnitude
regardless of the random phase. The gradient area of the stabilizer
must be carefully chosen since motion smaller than the slice thickness
between the stabilizer and echo adds constant phase. This affects
extended readouts because later echoes will be phase offset relative to
early echoes, reducing apparent resolution. We
mitigate this by applying a stabilizer area only twice the maximum slice
phase encode area. This creates ripple artifacts from partially rephased
T1-recovered fat, which we reduce by applying an elliptical
partial Fourier mask.
Respiratory motion:
A 2D-EPI image is used for binning data into respiratory states. The
respiratory signal was extracted from the first principal component of
concatenated respiratory navigators3. This strategy requires that
respiratory navigators have the same contrast. Since diffusion contrast
varies between shots due to motion, the respiratory navigator is placed
before diffusion preparation.
Image-based shot weighting: Because
the degree of motion varies within the volume, diffusion gradients may
annihilate signal in certain regions. Instead of discarding entire
shots, we adopt an image-based per-shot weighting to deemphasize data
overly corrupted by diffusion gradients4. The weighting is obtained
from complex phase navigator images as the first right singular
vector of local xyz-shots matrices, similar to Walsh coil estimation5.
The weighting is a k-space convolution but is efficiently computed
using zero-padded FFTs.
Reconstruction: The
weighted least-squares with 1D-TV penalty along respiratory phases6 (Eq 1.)
was solved with FISTA7. In Equation 1, W is the image-based per-shot
weighting, Y-measured k-space, D-sampling, F-FFT, P-phase navigator, S-coil
sensitivities, X-image for each respiratory phase. The 1D-TV proximal operator
was solved with gradient descent. Figure 1 shows the sequence and
reconstruction pipeline.$$\min_X ||W^{\frac{1}{2}}(Y-DFSPX)||_2^2+\lambda_{TV}||\nabla_RX||_1\,\,\,\,\,\,(\mathrm{Eq}\,1.)$$
Acquisition: Two
healthy volunteers (one male, one female) were scanned on a 3T Signa Premier (GE
Healthcare) following IRB approval and informed consent. Acquisition parameters
for coronal free-breathing DW-FLASH were: 4 respiratory bins, respiratory
navigator EPI-ETL 8 (readout S/I phase encode L/R), FLASH-TE/TR 1.4/3.5 ms, flip
angle ramp 5-8°, matrix size 256$$$\,×\,$$$192$$$\,×\,$$$24, voxel size 1.4$$$\,×\,$$$1.9$$$\,×\,$$$5 mm, spine$$$\,$$$+$$$\,$$$AiR
coil (GE Healthcare), diffusion axes L/R+A/P, ETL 90/40 lines randomly sample center 16$$$\,×\,$$$8 region,
TEprep/TR 60/1600 ms, 140 shots, scan time 7:40 for b=0/500$$$\,$$$s/mm2,
ASPIR fat suppression, stabilizer 2 and 4 cycles/cm. B1-insensitive optimal control
pulses8 were used for preparation. Coil sensitivities were estimated from
time-averaged b=0$$$\,$$$s/mm2 images using ESPIRIT9, SVD compressed from 56
to 24 channels, reconstruction ~25 minutes (2 NVIDIA Titan GPUs, 128
GB RAM). Respiratory-triggered 2-shot DW-EPI MUSE1 was acquired with identical
FOV and 2 NEX, scan time 3:32, 6 slices/trigger, TE 55 ms, ASPIR.
Results
The effects of transient fat signal rephased during
the readout is shown in the respiratory resolved images of Figure 2. Partial
Fourier masking reduces these artifacts.
Figure 3 shows the effect of high stabilizer area,
which sensitizes the resolution to subvoxel motion. A smaller stabilizer area
improves apparent resolution but introduces transient fat signal.
Figure 4 shows a comparison with respiratory-triggered
DW-EPI. Distortion in EPI is evident in the bowels and other organs. The
proposed method is distortionless and has similar contrast.
Figure 5 shows the benefit of shot weightings computed
from phase navigators. Signal recovery is improved beneath the diaphragm, an
area with high motion.Discussion
We have presented a distortionless free-breathing
diffusion weighted sequence. Although M1-nulling is employed, the DW sequences
do not recover all signal under the diaphragm. Future work includes
verifying ADCs under free-breathing, interleaved fat saturation
during readout, and prospective partial Fourier.Conclusion
Distortionless, volumetric, diffusion weighted
images can be obtained during free-breathing.Acknowledgements
NIH R01-EB009055, NIH R01-CA249893, GE Healthcare, Karolinska Foundation for pulse programming assistance.References
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