Carlos Milovic1,2,3, Mathias Lambert1,2,3, Christian Langkammer4, Kristian Bredies5, Cristian Tejos1,2,3, and Pablo Irarrazaval1,2,3
1Department of Electrical Engineering, Pontificia Universidad Catolica de Chile, Santiago, Chile, 2Biomedical Imaging Center, Pontificia Universidad Catolica de Chile, Santiago, Chile, 3Millennium Nucleus for Cardiovascular Magnetic Resonance, Santiago, Chile, 4Department of Neurology, Medical University of Graz, Graz, Austria, 5Institute of Mathematics and Scientific Computing, University of Graz, Graz, Austria
Synopsis
L2-norm based data fidelity terms in QSM
functionals account for Gaussian noise in the phase or complex
domain. These approaches are not robust against phase
inconsistencies, such as artifacts from previous steps, intra-voxel
dephasing, etc. To deal with these errors and to suppress streaking
artifacts we present L1-norm algorithms that correct for
salt-and-pepper noise. We use simulations and in-vivo acquisitions to
show their streaking suppression capabilities. Furthermore, L1
methods do not require magnitude information, and they were able to
achieve similar results without ROI masks. This may facilitate
susceptibility studies of cortical areas and regions outside the
brain.
PURPOSE
Estimating the susceptibility of tissues is
an ill-posed inverse problem, prone to noise amplification and
artifact generation1,2.
The most prominent artifact is the so-called streaking artifact.
Phase inconsistencies to the expected magnetization field are
projected along the magic cone in the deconvolution process.
Traditionally, streaking artifacts are reduced using regularizers, at
the expenses of losing image sharpness or details3-5.
Modifications to the data fidelity term to account for more realistic
noise models have been able to further reduce the impact of streaking
artifacts, especially those arising from regions with low MR
signal6-8.
Unfortunately, these models require accurate signal magnitude
representations, and masks that rejects erroneous phase data. This is
often a complex task that may lead to the loss of cortical areas due
to size reduction of the region of support (erosion of the tissue
mask). Here we present two new data fidelity terms that model
salt-and-pepper noise to account for phase inconsistencies and
prevent streaking, one in the (linear) phase domain, and the other in
the (nonlinear) complex image domain.METHODS
In a Bayesian approach, the nonlinear QSM
method models Gaussian noise in the
complex image domain6-8.
A magnitude-weighted linear data fidelity term may be interpreted as
a first-order approximation8.
In this work, we compare the traditional linear and nonlinear L2-norm
models with two L1-norm alternatives: $$$argmin_{\chi }\frac{1}{2}\|W\left(F^{H}DF\chi-\varphi\right)\|_1+TV(\chi)$$$ and $$$argmin_{\chi }\frac{1}{2}\|W\left(e^{iF^{H}DF\chi}-e^{i\varphi}\right)\|_1+TV(\chi)$$$, where W is a
magnitude-based weight or ROI mask, D is the frequency dipole kernel,
F the Fourier transform with FH its inverse, Φ
the input local phase and χ
the susceptibility distribution. For
simplicity, we use TV as the regularization. To reduce computational
processing time, we solved these optimization problems using ADMM. To
decouple the linear data fidelity term, an auxiliary variable
$$$z=F^HDF\chi-\varphi$$$ is needed. For the nonlinear data fidelity term, two additional
auxiliary variables $$$z_1=F^HDF\chi$$$ and
$$$z_2=e^{iz_1}-e^{i\varphi}$$$ are needed. Then, the z,
z1,
z2,
and χ
subproblems are solved in a similar way as in Bilgic9
and Milovic8,10,
using a proximal operation for z
and z2.
We use internal Newton-Raphson
iterations to solve z1.
These solvers were compared using forward
simulations from a COSMOS (complex noise, SNR=100) reconstruction
(QSM Challenge 1.0 dataset11)
with different W weights (no ROI mask, ROI masks, and SNR weights). We
also used one simulated acquisition from the QSM Challenge 2.0
dataset12.
We used the provided frequency map from the Sim2SNR2 data as input,
due to its high noise level and intra-voxel dephasing effects. In
vivo reconstructions are also provided, using the QSM Challenge 1.0
dataset.RESULTS
Figure 1 presents different reconstructions
varying the ROI mask (with and without) and introducing magnitude
weights (W).
Regularization parameter was
obtained optimizing RMSE (Table 1).
Notably, L1 reconstructions without masks or magnitude information
were possible, with similar visual results to those masked. Without
phase inconsistencies inside the ROI, L2-norm methods achieved better
metric scores. Figure 2 and Table 2 show the results of
reconstructing the Challenge 2.0 dataset. L1 reconstructions achieved
lower errors for all metrics. Nonlinear reconstructions performed
slightly better than their linear counterparts. In vivo
reconstructions (Figure 3) show less streaking from the venous system
and more structural details -especially at cortical regions- for the
L1 methods.DISCUSSION & CONCLUSION
Despite having slightly worse global
metrics in the first experiment (RMSE and SSIM, Challenge 1.0), L1
reconstructions seemed to be more robust against phase noise,
producing sharper images. Irrespective of the data fidelity weight or
the mask used, L1 methods produced optimal reconstructions with similar
associated regularization weights, within one order of magnitude.
L2-norm methods had optimal regularization weights depending on the
mask or weight in a range larger than two orders of magnitude. This
makes parameter fine-tuning easier for L1-norm methods. L1
reconstructions were also more robust to phase errors, making the ROI
masking process less relevant. This may allow QSM algorithms to
better explore cortical areas and may facilitate reconstructions of
regions outside the brain. It also prevents streaking from strong
intra-voxel dephasing effects, as seen in the Challenge 2.0 dataset,
where L1 reconstructions performed significantly better and were more
robust to noise at the venous system. The nonlinear L1 method seemed
to produce smoother results than the linear method, without loss of
information.Acknowledgements
Fondecyt 1191710, Anillo 190064,
Millennium Nucleus for
Cardiovascular Magnetic ResonanceReferences
1. Wharton CMRB 2005. 2. Shmueli MRM 2009.
3. de Rochefort MRM 2008. 4. Kressler IEE-TMI 2010. 5. Liu MRM 2011.
6. Liu MRM 2013. 7. Wang IEE-TBE 2013. 8. Milovic MRM 2018a. 9.
Bilgic SPIE 2015. 10. Milovic MRM 2018b. 11. Langkammer MRM 2018. 12.
Marques ISMRM 2019.