Jingyuan Lyu1, Qi Liu1, Zhongqi Zhang2, Jian Xu1, and Weiguo Zhang1
1UIH America, Inc., Houston, TX, United States, 2United Imaging Healthcare, Shanghai, China
Synopsis
This
abstract presents a new approach to accelerated T1 mapping of the heart under
free-breathing and without ECG. Compared with traditional radial sampling
trajectory, spiral sampling offers the possibility to get ride of navigator
data in the framework of “multitasking”, though at an extra cost of increased
susceptibility to system imperfections such as gradient delay.
Introduction
As an important biomarker, quantitative T1 mapping was used
for various diseases diagnosis [1]. T1 cardiac magnetic resonance (CMR) offered
by multitasking [2] is a free-breathing, ECG-free technique featuring high
spatial and temporal resolution myocardial T1 mapping, by utilizing low-rank
tensor imaging model [2,3] to solve multiple ‘tasks’ at the same time.
Despite its ability to produce 2D T1 cine maps in a short 1-min
scan, T1 CMR multitasking is capped at 50% efficiency due to scan time spent on
navigator readouts that had limited contribution to spatial basis. Navigator
lines of a constant k-space trajectory between imaging lines were needed for
temporal subspace estimation in standard CMR Multitasking [2].
This abstract presents a new approach to
accelerated T1 mapping of the heart under free-breathing and without ECG. The
proposed approach is still within the “multitasking” framework, but requires no
navigator data. In data acquisition, imaging data was acquired continuously using
2D spoiled-GRE sequence with variable-density spiral trajectories updated with
the golden angle. In image reconstruction, the temporal basis is first
estimated from the central densely sampled spiral k-space data within a chosen
radius. Respiratory motion, cardiac motion, inversion recovery images, and T1
cine maps were then reconstructed using multitasking framework.Methods
1. Sequence design: A pulse sequence based on 2D spiral
spoiled-GRE was developed. Consecutive spiral leaves are rotated by the golden
ratio angle of 137.5° such
that each new spiral leaf is sampling a substantially different part of k-space
compared to the immediately preceding leaf.
Imaging Parameters: All data were acquired on a clinical 1.5T
scanner (uMR 570, United Imaging Healthcare, Shanghai, China).
Imaging
parameters: TR/TE=6.40/0.91ms, Flip angle=5°, FOV=250x250mm2, slice thickness=8mm,
matrix size = 160x160, 15-channel cardiac coil. The spiral trajectory was
designed using the maximum available gradient strength and slew rate, assuming
16 interleaves to cover the entire k-space, and using 4 times undersampling at
the peripheral of k-space [5].
2. Gradient delay correction: Spiral readout
trajectory was corrected using a gradient system response model that has been
previously calibrated. Each spiral trajectory was individually processed for
actual trajectory before image reconstruction.
3. Reconstruction: The underlying multidimensional image was
represented by a 4-way tensor $$$\mathcal{A} =I(x,c,r,τ)$$$. The
first dimension concatenating all image pixel locations and other dimensions
indexing cardiac-motion, respiratory-motion, and inversion recovery. The tensor
can be decomposed in the partially separable form $$$\mathcal{A}_{(1)} = \textbf{U}_{\textbf{x}} \Phi$$$, where $$$\mathcal{A}_{(1)}$$$ is
the mode-1 matricization of $$$\mathcal{A}$$$ and $$$\textbf{U}_{\textbf{x}}$$$ is
the spatial basis, $$$\Phi$$$ is the multi-dimensional temporal basis.
Initialization
of $$$\underline{\Phi}$$$
Spiral sampling offers a variable density k-space coverage
where the undersampling rate is much lower around k-space center than the
outer, as shown in Figure 1. Therefore,
a low spatial resolution image from each spiral can be reconstructed and used
for temporal basis estimation. [4] The initial temporal basis $$$\Phi$$$ is
first estimated from the central part of the undersampled spiral k-space data
within a chosen radius. These data can be used to obtain a series of low spatial
resolution but high temporal resolution images, represented in matrix $$$\Gamma_{LR}$$$.
Then $$$\Phi$$$ can be obtained from the R dominant right singular vectors
through the singular value decomposition (SVD).
Calculation
of $$$\underline{\textbf{U}_{\textbf{x}}}$$$
$$${\textbf{U}_{\textbf{x}}}$$$ can
be recovered by solving the optimization problem:
$$\widehat{\textbf{U}_{\textbf{x}}} =
\mathop{argmin}\limits_{\textbf{U}_{\textbf{x}}}
||\textbf{d}-\textbf{E}(\textbf{U}_\textbf{x}\Phi)||_2^2+R(\textbf{U}_\textbf{x})
$$
where $$$\textbf{d}$$$ is the acquired imaging data, $$$\textbf{E}(\cdot)$$$
describes multichannel MR encoding with undersampling operator, and $$$R$$$
is spatial regularization operator.Results
Figure
1 depicts the spiral sampling trajectory used in self-navigated spiral multitasking.
The densely sampled central k-space can be used to generate a series of very
low-resolution images $$$\gamma(\textbf{x},t_1)\cdots \gamma(\textbf{x},t_N)$$$, which
form a low rank matrix $$$\Gamma_{LR}$$$. Figure 2 illustrates typical volunteer cardiac imaging results
reconstructed from the proposed method.
Figure 3 shows typical diastole and systole T1 maps.Conclusion and Discussion
To our best knowledge, we have implemented the first spiral,
navigator-less, T1 free-breathing cardiac MRI under the framework of
multitasking. Compared with traditional radial sampling trajectory, spiral
sampling offers the possibility to get ride of navigator data in multitasking,
though at an extra cost of increased susceptibility to system imperfections
such as gradient delay.Acknowledgements
This work was partially facilitated by a non-exclusive
license agreement between Cedars-Sinai Medical Center and United Imaging
Healthcare.References
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