Xinwei Shi1,2, Evan G Levine1,2, and Brian A Hargreaves1,2
1Radiology, Stanford University, Stanford, CA, United States, 2Electrical Engineering, Stanford University, Stanford, CA, United States
Synopsis
3D Multi-Spectral Imaging (MSI) methods, including SEMAC, MAVRIC, and
MAVRIC-SL, enable MRI near metallic implants by correcting for the
metal-induced off-resonance artifacts, but their widespread application is
limited by prolonged scan time. In this work, we introduce a novel model-based
reconstruction method to accelerate 3D MSI. We demonstrate in phantom and in vivo experiments that the proposed
method can accelerate MAVRIC-SL acquisitions by a factor of 4 when used alone, and
13-17 when combined with parallel imaging and half-Fourier acquisition. The images
reconstructed by the proposed method showed sharper details and lower level of
noise, compared with model-free L1-ESPIRiT. INTRODUCTION
MRI has the potential to provide excellent soft tissue
contrast for diagnosing complications surrounding metallic implants. However,
the presence of metal induces $$$B_0$$$ field perturbations and
causes severe image distortions. 3D Multi-Spectral Imaging (MSI) methods,
including SEMAC
[1], MAVRIC
[2], and MAVRIC-SL
[3],
are able to correct for the metal-induced off-resonance artifacts, but at a
cost of prolonged scan time. In this work, we introduce a novel model-based method to accelerate 3D MSI. We demonstrate in phantom and
in vivo experiments that the proposed method can accelerate MAVRIC-SL
acquisitions by a factor of 4 when used alone, and 13-17 when combined with
other acceleration methods.
THEORY
In MAVRIC-SL or SEMAC, thin slices are excited, and 3D spatial encoding with
view-angle tilting (VAT)[4] is used to resolve the distorted slice
profile (Fig.1A). Conventionally, the 3D images of different spectral bins
(distorted slices) are reconstructed separately, including prior
compressed-sensing approaches[5,6]. We propose to exploit the signal
model (Fig.1 BC) of the spectral bins to reduce the unknowns from over 20 bin
images to 2 parameter maps.
The image of spectral bin b is
represented by $$$m_b(\rho(\textbf{r}),f(\textbf{r}))=\rho(\textbf{r})\cdot G(f(\textbf{r})-f_b)\quad \mathrm{(1)}$$$, where $$$G(f)$$$ is the
frequency profile of RF pulses and $$$f_b$$$ is the
center frequency of the bin. $$$G(f)$$$ and $$$f_b$$$ are usually known for
a given sequence. The parameters to be estimated include the $$$B_0$$$ field map $$$f(\textbf{r})$$$, and the magnetization map $$$\rho(\textbf{r})$$$. If $$$M_b$$$ represents the
under-sampling mask of bin b, F{} represents
the Fourier transform, the acquired k-space of the bin is $$$y_b=M_b \cdot F\{\rho(\textbf{r})G(f(\textbf{r})-f_b)\}$$$. The proposed method directly solves for $$$\rho(\textbf{r})$$$ and $$$f(\textbf{r})$$$ using k-space data of
all bins as, $$\mathrm{minimize}_{\rho(\textbf{r}),f(\textbf{r})}{\Sigma_b{\|M_b \cdot F\{\rho(\textbf{r})\cdot G(f(\textbf{r})-f_b)\} -\hat{y}_b \|_2^2} + \lambda\mathrm{TV}(\rho(\textbf{r}))}, \quad \mathrm{(2)}$$
where TV represents the
total variation. A nonlinear conjugate gradient algorithm[7,8] is used to solve $$$\mathrm{(2)}$$$.
METHODS
The
reconstruction procedure is outlined in Fig. 2. The raw k-space
data should be demodulated at a single frequency for all bins before solving $$$\mathrm{(2)}$$$, so that
off-resonance and VAT will induce the same pixel
displacements in
the readout direction for all bins. To correct for the distortions in the resulting
parameter maps, the bin images $$$m_b$$$ are synthesized based on $$$\mathrm{(1)}$$$, and
then demodulated at the center frequency of each bin. In the final step, the
bin images are summed to a composite image.
The
proposed method was tested in a MAVRIC-SL scan of an agar gel phantom with a Ti/CoCr shoulder prosthesis on a GE 3T MRI system. The fully
sampled data were retrospectively under-sampled by a factor of 3.8 using
Poisson-disc sampling (Fig.3A). Different
(randomly selected) under-sampling patterns were applied to different bins. The
proposed method, integrated with 2x2 parallel imaging and half-Fourier
acquisition, was compared with a bin-by-bin L1-ESPIRiT[9] reconstruction, in a
MAVRIC-SL hip scan with a total hip replacement on a GE 1.5T MRI system. The acquired k-space data were further
under-sampled by factors of 2 and 3 by multiplying the uniform sampling mask (Fig.4A) with Poisson-disc sampling masks (Fig.4CF). The scan parameters are detailed in Table 1.
RESULT & DISCUSSION
In
the phantom experiment (Fig.3), the proposed model-based reconstruction was
applied alone without other acceleration methods, and the composite image
reconstructed with 26% sampled data preserved most fine structures. The
results of proposed method in the in vivo
scan (Fig.4) demonstrated sharper details compared with L1-ESPIRiT at both
2x and 3x additional subsampling. In
both phantom and in vivo results, the
reconstructed image showed improved SNR compared with the reference images and
L1-ESPIRiT results, likely because the fitting suppressed noise and slice-direction
ringing that was not consistent with the model.
In
the in vivo scan, artificial signal
oscillations appeared in a small area above the implant with the
proposed method (dashed arrows in Fig.4), which was more obvious at 3x
additional subsampling. This was caused by imperfection of the model where the
spins in one voxel have largely varying off-resonance frequencies. The large off-resonance gradient also caused pile-up artifacts in the reference images and L1-ESPIRiT results[10].
Currently, the same uniform
under-sampling was applied to all bins prospectively in the in vivo scan. Using prospective under-sampling
with different patterns for each bin will probably improve the quality of
reconstructed images, and permit a higher under-sampling factor.
CONCLUSION
By
incorporating the signal model of 3D MSI, the proposed model-based reconstruction is able to provide high-quality images near metallic
implants using 4x under-sampled k-space, as demonstrated in the phantom
experiment. We also demonstrated
in vivo
that the proposed method can be integrated with partial Fourier and parallel
imaging and further accelerate MAVRIC-SL by a factor of 2 to 3.
Acknowledgements
NIH
R01 EB017739, R21
EB019723, P41 EB015891,
research support from GE Healthcare.References
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