Yibo Zhao1,2, Rong Guo1,2, Yudu Li1,2, Keith R. Thulborn3, and Zhi-Pei Liang1,2
1Department of Electrical and Computer Engineering, University of Illinois, Urbana-Champaign, Urbana, IL, United States, 2Beckman Institute for Advanced Science and Technology, University of Illinois, Urbana-Champaign, Urbana, IL, United States, 3Center for Magnetic Resonance Research, University of Illinois at Chicago, Chicago, IL, United States
Synopsis
Quantitative
sodium MRI is a unique tool for assessing tissue viability noninvasively. A major
obstacle to widespread clinical applications of sodium MRI is low sensitivity, which leads to low spatial resolution even with long scan times. We present a
novel method for reconstruction of high-resolution sodium maps from noisy,
limited k-space data. The proposed method has been validated using simulated
and experimental data,
producing high-SNR and high-resolution tissue
sodium concentration maps.
These high-resolution maps were also shown to improve the detection of tumor responses
to radiation therapy.
Introduction
Tissue sodium concentration (TSC) has long
been recognized as a quantitative indicator of ion homeostasis that reflects
tissue viability.1-3 Quantitative sodium MRI techniques have been developed and used to measure
TSC in the human brain non-invasively, successfully
detecting tumor responses to therapy4,5 and neural cell death in Alzheimer’s
disease6.
However,
clinical applications of sodium MRI remain impeded by several longstanding
technical challenges, including low sensitivity, fast biexponential T2
relaxation, long data acquisition time and low spatial resolution.3,7 Significant advances have been made in
the past decades to address these challenges, from hardware development8,9 to novel pulse sequences10-15. However, the
capabilities of sodium MRI at 3T are still rather limited, with nominal spatial
resolution around $$$5\times5\times5$$$ mm3 and data acquisition time on the order of
10 minutes.13
Constrained
reconstruction methods, such as compressed sensing16,17 and anatomically
constrained reconstruction18,19,
have recently emerged to enhance SNR and resolution and reduce
artifacts in sodium MRI. Although compressed sensing has been used to remove or
reduce noise-like artifacts, its practical performance has been limited due to
low SNR and limited k-space coverage of the acquired data. Constrained
reconstruction incorporating anatomical prior
information from high-quality proton image can also enhance SNR and spatial resolution
for image features evident in the companion proton image, but with a limited capability
to reconstruct sodium-dependent novel features (e.g., lesions). In addition, anatomically
constrained reconstruction is known to be sensitive to inter-scan subject motion,
which affects their robustness needed for practical applications.
We
have developed a new method for reconstruction of high-quality sodium images
from noisy, limited k-space data in the presence of inter-scan subject motion.
The new method has been tested using simulated and experimental data from
human subjects, producing significantly better results than the existing
methods. The high-resolution sodium concentration maps obtained using our new
method were also shown to improve the detection of tumor responses to radiation
therapy. Methods
Our proposed method, illustrated in Fig.
1, synergistically integrates motion-compensated constrained reconstruction
with compressed sensing for reconstruction of high-quality sodium images from
noisy, limited k-space data. The key features of our method
include: (a) use of anatomical prior information for denoising and resolution
enhancement, (b) built-in capability for detection and correction of inter-scan
subject motion, and (c) use of sparsity constraints for effective recovery of
sodium-dependent novel features.
More specifically, our proposed method represents
the desired sodium image $$$\rho(\boldsymbol{x})$$$
using the following model:
$$\rho(\boldsymbol{x})=\sum_{m=-M}^{M} \alpha_m \rho_{\mathrm{ref}}(\boldsymbol{x};\boldsymbol{\theta})e^{-i2\pi m\Delta \boldsymbol{k\cdot x}}+\rho_{\mathrm{s}}(\boldsymbol{x}),\\
\mathrm{subject~to~}\|\Phi(\rho_{\mathrm{s}}(\boldsymbol{x}))\|_1\le\varepsilon,$$
where $$$\rho_{\mathrm{ref}}(\boldsymbol{x};\boldsymbol{\theta})$$$ represents a motion-compensated reference, $$$M$$$ the order of the generalized series (GS) model20, $$$\alpha_m$$$ the GS coefficients, $$$\rho_{\mathrm{s}}(\boldsymbol{x})$$$ an image component which is forced to be sparse under sparsifying transform $$$\Phi$$$. As compared with the conventional Fourier
model, the proposed model enables the effective use of a priori information for
denoising and resolution enhancement. As compared with the modern compressed
sensing model, the proposed model enables better use of the measured data and
the sparsity constraint for recovery of novel image features by modeling the
“prior” and “novel” components separately.
To generate the reference $$$\rho_{\mathrm{ref}}(\boldsymbol{x};\boldsymbol{\theta})$$$, we first segment the proton image into different tissue compartments,
then estimate the average sodium concentration of each tissue compartment
$$\{\hat{c}_r\}=\arg\min_{\{c_r\}}\left\|d(\boldsymbol{k}) - \Omega\mathcal{F}\left\{\sum_{r=1}^{R} c_rM_r(\boldsymbol{x})\right\}\right\|_2^2.$$
Then compartmental concentration variations are reconstructed using the
GS model
$$\{\hat{\alpha}_m\}=\arg\min_{\{\alpha_m\}}\left\|d(\boldsymbol{k}) - \Omega\mathcal{F}\left\{\sum_{m=-M}^{M} \alpha_m\left(\sum_{r=1}^{R} \hat{c}_rM_r(\boldsymbol{x})\right)e^{i2\pi m\Delta \boldsymbol{k\cdot x}}\right\}\right\|_2^2.$$
To avoid potential image reconstruction
artifacts due to inter-scan subject motion, our model also includes a built-in
capability for motion estimation and correction.
We finally use sparsity constraint to recover
the novel features by solving the following problem:
$$\hat{\rho}_{\mathrm{s}}(\boldsymbol{x})=\arg\min_{\rho_{\mathrm{s}}(\boldsymbol{x})}\|d(\boldsymbol{k})-\Omega\mathcal{F}\left\{\hat{\rho}_{\mathrm{ref}}(\boldsymbol{x};\boldsymbol{\theta})+\rho_{\mathrm{s}}(\boldsymbol{x})\right\}\|_2^2 + \lambda\|\Phi(\rho_{\mathrm{s}}(\boldsymbol{x}))\|_1.$$
Our method has a distinct advantage over
the conventional sparsity-constrained reconstruction methods for solving the
sodium imaging problem because of its ability to “remove” the “prior” component
so that the sparsity constraint is applied to $$$\rho_{\mathrm{s}}(\boldsymbol{x})$$$ only. Since $$$\rho_{\mathrm{s}}(\boldsymbol{x})$$$ is much sparser than the overall image $$$\hat{\rho}_{\mathrm{ref}}(\boldsymbol{x};\boldsymbol{\theta})+\rho_{\mathrm{s}}(\boldsymbol{x})$$$, the sparsity constraint is more
effective for recovery of the sodium-dependent novel features that are not
present in the companion proton image.Results
Our method has been validated using simulated and experimental data, producing high-SNR and high-resolution TSC maps. Figure 2
shows reduction in noise level and improvement in spatial resolution provided
by our method in the presence of novel features in a Monte-Carlo
simulation study. Figure 3
shows some representative high-quality reconstructions from phantoms and
healthy subjects. Linear calibration curves with small variances from the
phantom data and reproducible TSC values across different brain regions and
different subjects were obtained. Figure 4
shows the capability of our method to resolve small anatomical
structures and to reduce partial volume effects from surrounding CSF. Figure 5
shows high-resolution TSC changes in response to treatment in a tumor patient.
The TSC decline detected by the proposed method indicated the return of
infiltrated brain tissue to normal cell packing.Conclusions
A
novel method for high-resolution sodium imaging has been proposed to provide an
effective solution to the low resolution and low SNR problems that have limited clinical
applications of sodium imaging. Simulated and experimental results have
successfully demonstrated the feasibility of achieving high-quality TSC maps using
the proposed method. The
reduction in partial volume effects was shown to improve the detection of tumor
responses to radiation treatment.
Acknowledgements
The
authors acknowledge Dr. Ian C. Atkinson and Dr. Aiming Lu for useful
discussions about image reconstruction from twisted projection data and for
handling p-files from GE 3T scanner. The work reported in this paper was
supported, in part, by the National Institutes of Health (NIH); contract grant
number: KRT RO1 CA1295531-01A1.References
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