Lyu Li1, Sheng Fang2, Pascal Spincemaille3, Bida Zhang4, Yi Wang3,5, and Hua Guo1
1Center for Biomedical Imaging Research, Department of Biomedical Enginnering, School of Medicine, Tsinghua University, Beijing, China, People's Republic of, 2Institute of nuclear and new energy technology, Tsinghua University, Beijing, China, People's Republic of, 3Radiology, Weill Cornell Medical College, New York, NY, United States, 4Healthcare Department, Philips Research China, Shanghai, China, People's Republic of, 5Biomedical Engineering, Cornell University, New York, NY, United States
Synopsis
High spatiotemporal resolution 3D imaging is a desired technique for
detecting dynamic information of detailed anatomy and getting accurate modeling
parameters. In this abstract, we developed a method using golden angle spiral
and compressed sensing with L0 homotopic minimization for high resolution 3D
imaging. In this method, a high undersampling rate and high motion insensitivity
can be achieved. In clinical applications such as dynamic contrast enhanced MRI,
this new method is very promising to achieve high spatiotemporal resolution without
breath-hold.Purpose
High spatiotemporal resolution 3D imaging is a desired technique for
detecting dynamic information of detailed anatomy and getting accurate modeling
parameters. However, low efficiency of MR signal acquisition and motion artifacts
are always challenging in dynamic MRI. Recently radial sampling is widely used
because of its high motion insensitivity. Additionally, a complement reconstruction
method called GRASP
[1] was developed for high spatiotemporal 3D dynamic
imaging. As a matter of fact, we once proposed a method using golden angle
spiral for 3D dynamic imaging
[2], in which compressed sensing (CS) with L1
minimization was used and the spatiotemporal resolution was improved greatly.
We call this method spiral
sparse parallel imaging
(SpiralSP-L1). To improve the temporal resolution and accuracy further, CS with
L0 minimization is investigated
[3] for the spiral data reconstruction (SpiralSP-L0)
in this abstract, which provides high image quality as well as high temporal precision.
Methods
Simulations were performed on a numerical phantom (Fig. 1). In the
phantom, a large disc moved from the right side to the left; and the contrast
in a small disc was changing during the movement. There is also a small bright point
in the phantom which represents a detailed structure.
In-vivo experiments were performed on a GE 3T MR750 scanner (GE
Healthcare, Waukesha, WI) with an 8 channel coil. A 3D stack of golden angle
spiral was used to acquire k-space data. The scan parameters were
TR/TE=5.9ms/0.3ms, FOV=360×360×160mm3, in-plane resolution=1.41×1.41mm2,
slice thickness=5mm, interleave number for each slice=192, total scan
time=30sec. The subject was required to breathe shallowly when scanning. Compressed
sensing with homotopic L0 minimization [3] was used in the reconstruction. The
sparse domain was temporal total variation (TV) domain. The reconstruction
equation was shown as follows: $$\min\left\{\parallel
F\cdot S\cdot d\parallel_2^2+\lambda\cdot \lim_{\sigma \rightarrow
0}\sum_{n\in\Omega}(1-e^{-\frac{|u(n)|}{\sigma}})\right\}, u=T\cdot d$$In this equation, the first part is a SENSE item which guarantees the
data consistency ($$$d$$$ is the image series, $$$S$$$ is the sensitivity map, $$$F$$$
is the non-Cartesian Fourier transform, $$$m$$$ is the acquired data), and the
second part is an approximation of L0 norm ($$$T$$$ is a temporal TV operator
and $$$\lambda$$$ is a regularization parameter).
The fully sampled k-space data
for 1 frame (including simulation and in-vivo data)
consisted of 48 interleaves. We used 2 interleaves to reconstruct 1 frame,
corresponding to an acceleration factor of 24. With such a high undersampling
rate, the 3D temporal resolution for in-vivo data was about 312ms.
Results
Three reconstruction algorithms were compared with each other including
Temporal Resolution Acceleration with Constrained Evolution Reconstruction
(TRACER)
[4], SpiralSP-L1 and SpiralSP-L0. Two representative frames were selected
to evaluate the algorithms. Fig. 2 shows the simulation results. The result of
SpiralSP-L0 shows least motion artifacts and highest SNR. Furthermore, the
detailed structure (red arrow) can be preserved best. Fig. 3 shows intensity
curves from the small disc
region, in which we can see that the result of TRACER is too noisy and
SpiralSP-L1 has some smoothing effects. The result of SpiralSP-L0 has the best
temporal accuracy. The relationship between the temporal resolution and
temporal accuracy is shown in Fig. 4, which indicates that, for all algorithms,
the higher reconstructed temporal resolution is the more accurate the intensity
curve is. For the shallow breathing
in-vivo
data in Fig. 5, the results from SpiralSP-L0 also show the best image quality with
least artifacts and highest SNR.
Discussion
The CS theory is based on L0 norm minimization theoretically; however
solving this problem numerically is not straightforward. So L1 norm is commonly
used in the CS reconstruction. When the undersampling rate becomes higher, L1
norm cannot recover images well any more. In comparison, in this study, L0 norm
CS shows better reconstructed images than L1 norm. For TRACER, it exploits the
strong relationship between two consecutive frames. So TRACER is vulnerable to motion
and resultant images may show large intensity fluctuations. Because CS exploits
the relationship of all frames, it is immune to intensity fluctuations. For
detailed structures and temporal accuracy, sufficient spatiotemporal resolution
is desired, which requires a high undersampling rate. Considering the
acquisition efficiency and motion insensitivity of spiral, SpiralSP-L0 may be a
potential solution.
Conclusions
A new dynamic 3D imaging method is investigated
which combines golden angle spiral trajectories and the reconstruction
algorithm of CS with L0 minimization. This technique is highly motion
insensitive and acquisition efficient so that it is very promising to achieve
high spatiotemporal resolution imaging in clinical applications.
Acknowledgements
No acknowledgement found.References
1. Li Feng, et al.
MRM, 2014; 72:707–717
2. Lyu Li, et al.
ISMRM, 2015; 2448
3. Joshua Trzasko,
et al. IEEE TRANSACTIONS ON MEDICAL IMAGING, 2009; 28:106-121
4. Bo Xu, et al.
MRM, 2013; 69:370–381