Adam Berrington1,2, Michal Povazan1,2, and Peter B Barker1,2
1Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD, United States, 2F.M. Kirby Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD, United States
Synopsis
Spurious echo
artifacts appear in MRS spectra and originate from regions of unsuppressed and
insufficiently crushed signal. We propose a reconstruction method to remove such
artifacts using the sensitivity weighting of the receive channels at each spatial
location. Data from phantom and simulations show that spurious echoes can be separated
from underlying signal. The spatial distribution of unwanted signal was estimated
in vivo using B0 maps. Artifactual components of the signal were identified in sinus regions, however not entirely removed from the spectrum. Further work will aim to improve the conditioning of the
SENSE reconstruction to remove spurious echo artifacts from MRS data.
Aim
To
develop a reconstruction method based on sensitivity weighting of multiple
receive channels to separate artifactual signal from localized signal in MRS.Introduction
Ensuring
high quality spectra is critical for MRS to be implemented routinely in the
clinic.1 However, quality is often degraded by
the presence of spurious echo (or ghosting) artifacts, which overlap with
metabolite peaks and affect quantification.2 These artifacts arise from the excitation
and refocusing of unsuppressed water signal from outside the MRS voxel, which is
not properly crushed prior to acquisition.3 For instance, large susceptibility
gradients around the sinuses have been shown to be a source for such artifacts.4 Methods such as alternating slice
selection,4 optimizing crusher gradients,5 and deep learning,6 have been proposed to avoid or remove these
artifacts. Given that such artifacts originate from spatially distinct regions,
we propose a reconstruction method based on sensitivity encoding7 using multiple receiver coils to
separate these signals from the MRS signal. A similar approach was recently demonstrated
for dual-excited MRS voxels.8Methods
An
outline of the proposed method is shown in Fig.1 using a simulated
phantom9 in combination with 16 receiver coils ($$$K$$$).
Mean coil sensitivities, $$$S_{A_{j},k}$$$ at artifact regions, $$$A_{j}$$$ ($$$j=1\ldots N$$$) and voxel location, $$$V$$$, are calculated for each coil, $$$k$$$ ($$$k=1\ldots K$$$) generating a sensitivity
matrix of size $$$[N+1, K]$$$. As in SENSE MRI, the unfolding matrix, $$$U$$$ is calculated
from $$$S$$$ using the noise covariance of the channels, $$$\Psi$$$. Unfolding reveals spectra from the $$$N+1$$$ regions.
Scanning
was performed on a 7 T Philips Achieva MR system with dual-transmit/32-channel
receive array head coil. Sensitivity maps were median filtered
and normalized to a sum-of-squares image. Noise covariance was calculated from background voxels in
the sensitivity images.
Phantom
data were acquired from a GE ‘Braino’ Phantom (STEAM, TE/TR = 14ms/3s; NT = 32,
15x15x15mm3 voxel). Phantom data were reconstructed using a 3x1 grid
of ROIs with no prior estimate of artifact regions. Spectra were also acquired
from one volunteer (semi-LASER, TE/TR = 30ms/5s, NT = 64, 20x20x20mm3)
in a frontal voxel shimmed to second order. In order to maximize the artifact,
spoiler gradient amplitudes were reduced on all axes. To identify
regions of spurious echo in vivo, a B0
map was acquired with identical shim settings to the MRS scan. The B0
map was phase unwrapped10, smoothed and thresholded according to
the bandwidth (150 Hz) of VAPOR water suppression pulses in MRS (Fig. 2). The
subsequent image was segmented leaving regions of unsuppressed water in the
brain. SENSE unfolded data from MRS voxels were compared to weighted and
non-weighted channel-combined data.Results
Fig.
1 shows a simulated spectrum containing 3 singlet resonances (V) and 1 spurious
echo (A1) when using conventional channel combination. SENSE
reconstruction was subsequently able to separate these two signals, matching
the ground truth simulation.
In
the phantom, SENSE reconstructed signals (A1 and A2) from
outside the voxel contained pure spurious echo data occurring at two different time-points
in the FID (Fig. 3B) and revealed a somewhat cleaner region around the water
peak for the unfolded MRS voxel than normal channel combination (Fig. 3C),
although there was not complete removal of the artifact.
Reconstructed
spectra from one volunteer are shown in Fig. 4. Thresholding of the B0
image (Fig. 2) revealed 3 regions where residual water may be expected. One
region, A2, was positioned close to the voxel (V) in the central
sinus (g-factor = 1.4) and contained a large spurious echo component. Reconstruction
did not completely remove the artifact. However, when compared to normal channel-combined
data (Fig. 4C), the method was observed to produce cleaner spectra over the
spectral range (3-4) ppm than unweighted coil-combination and similar to
weighted combination.Discussion
A
straightforward reconstruction method is proposed to separate MRS signal from
spurious echo artifacts. Simulation and phantom results show there is potential
to identify artifact and MRS signal components based on sensitivity encoding. The
degree of artifact separation depends on precise knowledge of the artifact’s location
and, similar to parallel imaging, accurate sensitivity maps. Results in vivo support the previous finding
that spurious echoes often originate from the frontal sinus (Fig. 4).4 The artifact was not entirely removed
from the spectra. Gradient-echo sensitivity maps are vulnerable to signal
dropout in such regions, particularly at 7 T, hence may result in poor
estimation of sensitivities. Future work will endeavor to improve the quality
of the sensitivity maps through interpolation and filtering7 and include regularization terms11. In addition, the acquisition of residual
water suppression images (rWSI) (Fig. 5) may aid truer identification of artifact
regions.Acknowledgements
We would like to acknowledge the following funding support: NIH P41EB015909
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