ABOLFAZL MEHRANIAN1, Claudia Prieto1, Radhouene Neji1,2, Colm J. McGinnity3, Alexander J. Hammers3, and Andrew J. Reader1
1School of Biomedical Engineering and Imaging Sciences, King’s College London, London, United Kingdom, 2MR Research Collaborations, Siemens Healthcare Limited, Frimley, United Kingdom, 3School of Biomedical Engineering and Imaging Sciences, King’s College London & Guy’s and St Thomas’ PET Centre, London, United Kingdom
Synopsis
We propose a simple and robust methodology for synergistic
multi-contrast MR image reconstruction to improve image quality of undersampled
MR data beyond what is achieved from conventional independent reconstruction
methods. The advantages of the proposed methodology are threefold: i) it
exploits quadratic priors that are mutually weighted using all available MR
images, leading to preservation of unique features, ii) the weighting
coefficients are independent of the relative signal intensity and
contrast of different MR images and iii) the algorithm is based on a
well-established parallel imaging iterative reconstruction, which makes the
synergistic reconstruction of undersampled MR data clinically feasible
Introduction
MR data acquisition is often time consuming, particularly in
multi-contrast MR protocols. Partial Fourier and parallel imaging (e.g.
sensitivity encoding –SENSE) are conventionally employed
to reduce scan time by acquiring less k-space data than established by the
Nyquist criterion. Compressed sensing (CS) exploits the sparsity of the images
in a given domain to further reduce the acquisition time [1]. However, most of
these approaches reconstruct each contrast image independently, without taking
advantage of the redundant information in the multi-contrast direction. In this
work, we propose a framework for synergistic reconstruction of highly
undersampled multi-contrast MR data for improving upon independent parallel
imaging CS (i.e. total variation– TV– regularised SENSE)
reconstructions.Methods
Synergistic SENSE reconstruction of $$$n$$$ undersampled MR contrasts,$$${\boldsymbol{v}}^{\left(k\right)}$$$, is given by the following
minimization problem $${\left({\widehat{\boldsymbol{v}}}^{\left(1\right)},\dots
,{\widehat{\boldsymbol{v}}}^{\left(n\right)}\right)=\mathop{\mathrm{argmin}}_{{\boldsymbol{v}}^{\left(1\right)},\dots
,{\boldsymbol{v}}^{\left(n\right)}} \left\{\sum^n_{k=1}{{\left\|{\boldsymbol{E}}^{\left(k\right)}{\boldsymbol{v}}^{\left(k\right)}\mathrm{-}{\boldsymbol{s}}^{\left(k\right)}\right\|}^2_{{\boldsymbol{W}}^{\left(k\right)}}}\mathrm{+}\frac{{\beta
}_k}{2}{\left\|{\boldsymbol{D}}^{(k)}{\boldsymbol{v}}^{\left(k\right)}\right\|}^2_{{\boldsymbol{\xi
}}^{(k)}{\boldsymbol{\omega }}^{(k)}}\right\}\ }\ $$
where the first
term includes $$$n$$$ data fidelity terms and the second term is a multi-modal
weighted quadratic penalty function.
$$${\boldsymbol{E}}^{\left(k\right)}$$$ includes coil sensitivity maps and
k-space undersampling trajectories of $$$\textit{k}$$$th image contrast. $$${\boldsymbol{s}}^{\left(k\right)}$$$ is the acquired k-space data,
$$${\boldsymbol{W}}^{\left(k\right)}$$$ is the noise-correlation matrix between
coil channels, $$${\boldsymbol{D}}^{(k)}$$$ calculates intensity
differences between voxels of the $$$\textit{k}$$$th image in a local
neighbourhood, the elements of $$${\boldsymbol{\xi }}^{(k)}$$$ weight
these voxel differences based on their distance.$$$\ {\beta }_k$$$ are
regularization parameters. The elements of $$${\boldsymbol{\omega }}^{(k)}$$$
weight the difference between voxel $$$\textit{j}$$$ and $$$\textit{b}$$$ of the$$$
\textit{k}$$$th image in a local neighbourhood based on the product of Gaussian
similarity coefficients derived from all $$$n$$$ MR images, defined as:
$${\omega }^{\
}_{jb}=\frac{\mathcal{G}\left({\tilde{v}}^{\left(1\right)}_j,{\tilde{v}}^{\left(1\right)}_b,{\sigma
}_1\right)\dots \mathcal{G}\left({\tilde{v}}^{\left(n\right)}_j,{\tilde{v}}^{\left(n\right)}_b,{\sigma
}_n\right)}{\sum^N_{j=1}{\mathcal{G}\left({\tilde{v}}^{\left(1\right)}_j,{\tilde{v}}^{\left(1\right)}_b,{\sigma
}_1\right)}\dots \mathcal{G}\left({\tilde{v}}^{\left(n\right)}_j,{\tilde{v}}^{\left(n\right)}_b,{\sigma
}_n\right)} \ \mathcal{G}\left(q,r,\sigma
\right)=\frac{1}{\sqrt{2\pi }\sigma }{\mathrm{exp}
\left(-\frac{{\left(q-r\right)}^2}{2{\sigma }^2}\right)\ }$$
As a result,
Tikhonov regularization of the $$$\textit{k}$$$th image is guided by itself and the
complementary information available in other image contrasts. For the
calculation of the $$$\boldsymbol{\omega }$$$ coefficients, MR contrast
images are mutually registered during their reconstruction. The minimization
problem was solved using the conjugate gradient (CG) algorithm for each MR
contrast at each iteration (implemented in MATLAB), using the
$$$\boldsymbol{\omega }$$$ derived from all images from the previous iteration,
i.e. $$$\widetilde{\boldsymbol{v}}$$$. The proposed algorithm was compared to
iterative SENSE and TV regularized SENSE (TV-SENSE) reconstructions, optimized
using the alternating direction method of multipliers and CG algorithms.
Experiments
A patient with suspected mild cognitive impairment was scanned on a 3T
Biograph mMR scanner (Siemens Healthcare, Erlangen, Germany). Acquisitions were
performed for a 3D fully sampled T1-MPRAGE (resolution =
1.05$$$\times$$$1.05$$$\times$$$1.1 mm$$${}^{3}$$$, FOV = 235$$$\times$$$269$$$\times$$$191
mm$$${}^{3}$$$, TR/TE/TI = 1700/2.63/900 ms, flip-angle = 9º) and a 2x accelerated
3D FLAIR (resolution = 0.48$$$\times$$$0.48$$$\times$$$1.0 mm$$${}^{3}$$$, FOV =
245$$$\times$$$245$$$\times$$$160 mm$$${}^{3}$$$, TR/TE/TI = 5000/395/1800 ms, flip-angle =
120º) sequence. The k-space of the T1 data was retrospectively undersampled in
the phase and slice encoding directions by factors of 3 and 3 (R = 9).
Similarly, the FLAIR data was retrospectively undersampled by factors of 2 and
3 (R = 6)Results
Fig. 1 and 2 shows the results of synergistic reconstruction of undersampled
MR data, in comparison with fully sampled T1 and 2x undersampled FLAIR, as
reference reconstructions. SENSE and TV-SENSE reconstructions are also shown
for the undersampled dataset (T1: R = 9, FLAIR: R = 6). The results show that
TV-SENSE reduces aliasing artefacts however at the expense of blurring in the
T1 image and residual artefacts in the FLAIR image. As shown by the arrows,
synergistic reconstruction of the undersampled datasets reduces noise
amplification and remaining artefacts, and enhances the edges, especially in
the FLAIR imageDiscussion
Compared to previous reference-guided and joint reconstruction methods
[2,3], our proposed algorithm has a number of advantages, i) the weighting
coefficients are derived from all available MR images, which leads to
preservation of unique features. This should be advantageous in the case of
lesions visible only on certain sequences; ii) the weighting coefficients are
independent of the relative signal intensity and contrast of different MR
sequences, iii) the reconstruction algorithm is based on a widely used parallel
imaging algorithm. In addition, if one of the datasets is fully-sampled, the
synergistic reconstruction will still be beneficial for undersampled datasets
due to the preservation of unique features.Conclusions
The proposed synergistic reconstruction methodology aims to improve MR image quality by utilizing the boundary information common to different MR image contrasts and to provide a clinically feasible reconstruction algorithm. Our results using in-vivo data show the improved performance of the proposed method compared to standard separate reconstructions, therefore opening the way for more advanced reconstruction of undersampled data in routine practiceAcknowledgements
This work is supported by the Engineering and
Physical Sciences Research Council (EPSRC) under grant EP/M020142/1 and the Welcome
EPSRC Centre for Medical Engineering at King’s College London (WT
203148/Z/16/Z). The authors acknowledge financial support from the Department
of Health via the National Institute for Health Research (NIHR) comprehensive
Biomedical Research Centre award to Guy's & St Thomas' NHS Foundation Trust
in partnership with King's College London and King’s College Hospital NHS
Foundation Trust.References
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