Yunsong Liu1, Congyu Liao2, Daeun Kim3, Kawin Setsompop2, and Justin P. Haldar3
1Ming Hsieh Department of Electrical and Computer Engineering, University of Southern California, Los Angeles, CA, United States, 2Stanford University, Stanford, CA, United States, 3University of Southern California, Los Angeles, CA, United States
Synopsis
Multidimensional relaxation correlation spectroscopic
imaging methods have demonstrated powerful capabilities to resolve subvoxel
microstructure. In this work, we perform
T1-T2 relaxation correlation spectroscopic imaging using a sequence that
combines MR fingerprinting with a ViSTa preparation module to enhance
sensitivity to short-T1 components. We
demonstrate theoretically and empirically that this approach has advantages
over MR fingerprinting without ViSTa. Empirical
results demonstrate the ability to identify at least 6 anatomically plausible
tissue components, including a short-T1 component that was not previously
resolved when using MR fingerprinting without ViSTa. A novel generalized ADMM
algorithm is also proposed that substantially improves computational
efficiency.
Introduction
In recent years, several multicontrast acquisition and
multicomponent modeling techniques have emerged that can estimate the joint
distribution of T1 and T2 relaxation parameters within each voxel1-5.
These 2D relaxation distributions (or “2D relaxation correlation spectra”) can
be used to identify subvoxel microstructural tissue compartments that would
normally be hidden by partial volume effects. It has been proven theoretically that the use
of high-dimensional relaxation encoding can lead to multicomponent estimation
problems that are substantially better-posed than for lower-dimensional acquisition
methods4.
MR fingerprinting (MRF)6 is one of the
multi-contrast acquisition strategies that can be used to estimate 2D
relaxation correlation spectra1-3,5,7. Although MRF can be powerful,
it has also been observed that traditional MRF sometimes lacks sufficient
sensitivity to tissue compartments with short-T1 values (like the myelin water
component in brain tissue)7. In this work, we demonstrate the
ability to perform MRF-based multicomponent 2D relaxation modeling with
improved sensitivity to short-T1 components.
From an acquisition perspective, our approach combines
a traditional fingerprinting acquisition with a ViSTa preparation module to
better isolate short-T1 components, building off of a recent sequence concept
that was previously used for single-component tissue modeling9. From
a reconstruction/estimation perspective, we estimate multidimensional T1-T2 relaxation correlation spectroscopic images
(with 2 spectral relaxation dimensions and 2 spatial dimensions) using a previously
proposed spatially regularized estimation technique that offers substantial
estimation-theoretic advantages over approaches that do not exploit spatial regularity4,7. We also introduce a novel
generalized ADMM algorithm that substantially improves the computational
efficiency of this approach.Methods
A 2D ViSTa-MRF dataset (with 538 timepoints, and 32 spiral
interleaves to achieve fully sampled k-space) was acquired on a 3T Siemens
Prisma scanner with 1mm in-plane resolution and 10mm slice thickness. We used estimation-theoretic Cramer-Rao bounds
to compare the amount of information captured by the proposed ViSTa-MRF
sequence compared to a conventional MRF sequence.
Our estimation formulation assumes that we wish to estimate
a spectroscopic image corresponding to an $$$N_1 \times N_2$$$ spatial image matrix
and an $$$M_1 \times M_2$$$ T1-T2 correlation spectrum (with $$$M_1$$$ corresponding
to the number of T1 values and $$$M_2$$$ corresponding to the number of T2 values). Let $$$\boldsymbol{\alpha}_n \in
\mathbb{R}^{M_1M_2},\ n=1,2,...,N_1N_2$$$ represent the vectorized 2D spectrum at
the voxel $$$n$$$, and let the concatenated vector $$$\boldsymbol{\alpha} =
[\boldsymbol{\alpha}_1;\boldsymbol{\alpha}_2;\cdots;\boldsymbol{\alpha}_{N_1N_2}]
\in \mathbb{R}^{M_1 M_2 N_1 N_2}$$$ denote the vectorization of the full 4D
spectroscopic image that we wish to estimate.
Also let $$$\mathbf{d}_n \in \mathbb{R}^{N_t}$$$ denote the MRF time series
at voxel $$$n$$$, where $$$N_t$$$ is the number of time points, and let $$$\boldsymbol{\Phi} \in \mathbb{R}^{N_t \times M_1 M_2}$$$ be the MRF dictionary
such that we nominally have $$$\mathbf{d}_n = \boldsymbol{\Phi\alpha}_n$$$.
Following previous work4,7, we perform estimation
by solving a nonnegativity-constrained spatially-regularized least-squares
optimization problem:
$$\arg\min_{\boldsymbol{\alpha} \geq \mathbf{0}}
\sum_{n=1}^{N_1N_2}\frac{1}{2} \|\mathbf{d}_n - \boldsymbol{\Phi\alpha}_n\|_2^2
+ \frac{\lambda}{2} \|\mathbf{D}\boldsymbol{\alpha}\|_2^2$$
In this expression, $$$\lambda$$$ is a regularization parameter
and $$$\mathbf{D}$$$ is a spatial finite difference operator. The first term in the objective function
imposes data consistency and the second term imposes spatial regularization. The
use of spatial regularization substantially reduces the ill-posedness of the
estimation problem4.
To solve this optimization problem, we propose a
novel adaptation of the Generalized ADMM algorithm10 together with
the Sherman-Morrison-Woodbury formula11 to greatly simplify each of
the optimization subproblems. A
description of our proposed algorithm (with a comparison against the algorithm
used in previous work4,7) is shown in Figure 1.Results
Figure 2(a) shows a comparison of Cramer-Rao bounds for the
proposed ViSTa-MRF and conventional MRF sequences when estimating a
3-compartment model (comp. 1: T1/T2=120/20ms; comp. 2: T1/T2=750/60ms; comp. 3:
T1/T2=1300/75ms). As can be seen, the
proposed ViSTa-MRF sequence has a smaller Cramer-Rao bound for the short-T1 component
(comp. 1), suggesting that it encodes information about that component better
than the conventional MRF sequence.
Figure 2(b,c) shows the signal evolution curves for the three
components. It can be observed the for the ViSTa-MRF sequence, the first
timepoint of this curve provides excellent separation of the short-T1 component
(comp. 1) from the other two components.
Figure 3 shows spectroscopic imaging results, demonstrating
that we successfully resolve at least 6 anatomically plausible tissue
compartments, including a short-T1 component (comp. 5) that appears to be
consistent with myelin water (which was not visible in previous MRF-based 2D
relaxation spectroscopic imaging7).
Figure 4 shows that the estimated short-T1 component (comp. 5)
is consistent with the first point measured after the ViSTa module (which is
expected to contain only short-T1 components), although with better SNR and
with better separation from short-T1 extra-cranial tissue.
Figure 5 shows that the proposed algorithm
converges substantially faster than the previous algorithm.Conclusions
This work makes the novel observation that the combination
of ViSTa and MRF has good estimation-theoretic properties that can enable
better identification of short-T1 components in high-dimensional T1-T2
correlation spectroscopic imaging.
Empirical results demonstrate the ability to identify at least 6 anatomically
plausible tissue components, including a short-T1 component that was not
resolved when using MRF without ViSTa. We
also proposed a novel algorithm for estimating the high-dimensional
spectroscopic image that offers substantial computational advantages over the
previous algorithm.Acknowledgements
This work was supported in part by NIH grants R01-MH116173
and R01-NS0074980, as well as a USC Viterbi/Graduate School Fellowship.References
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