Jieying Zhang1, Simin Liu1, Yuhsuan Wu1, and Hua Guo1
1Center for Biomedical Imaging Research, Department of Biomedical Engineering, School of Medicine, Tsinghua University, Beijing, China
Synopsis
Simultaneous
multi-slab (SMSlab) technique is a 3D acquisition method that can achieve
optimal signal-to-noise ratio (SNR) efficiency for high-resolution diffusion-weighted
imaging (DWI) or functional MRI (fMRI). However, boundary artifacts may
restrain its application. Nonlinear inversion for slab profile encoding (NPEN)
has been proposed for its correction, which needs long computation time. In
this study, we propose to use a convolutional network for boundary artifacts
correction. It can solve the problem in a short time and improve the
signal-to-noise ratio (SNR), which is of great meaning for high-resolution
whole-brain DWI and fMRI.
Introduction
Simultaneous
multi-slab (SMSlab) acquisition1 is a combination of simultaneous multi-slice (SMS) and 3D
multi-slab techniques. In SMSlab, multiple 3D slabs are excited simultaneously
to achieve the optimal signal-to-noise ratio (SNR) efficiency. In this way, it
enables the acquisition of 3D high-resolution diffusion weighted images or
functional MR images2.
However, a remaining challenge, boundary artifacts, restrain the application of this
technique3-5. It
mainly results from truncated RF pulses and introduces intra-slab intensity
variation and inter-slab aliasing. Several methods were proposed to correct for
boundary artifacts for multi-slab acquisition3,4,6,7. They
can suppress the artifacts when the repetition time (TR) is long enough. Only
nonlinear inversion for slab profile encoding (NPEN)3,8 can
solve the problem at TR = 2000 ms, but its computation is time-consuming. It
won’t be practical when a large number of brain volumes are acquired.
After being trained by a sufficient amount of
high-quality data, a convolutional network (CNN) can solve a complex inverse
problem in 1 second9. Therefore, in this work, we investigate the
ability of CNN to correct for boundary artifacts for the SMSlab acquisition.Methods
Bloch simulation
was used to generate slab profiles of the SMSlab sequence1. 2 slabs were excited simultaneously (MB factor = 2). A 12-mm slab
thickness was used. Each slab contained 12 slices, 2 of which were overlapped
with the neighboring slabs. The slab thickness used in the refocusing pulse was
1.17 times as large as that of the excitation pulse. An interleaved slab
ordering was used. The simulation was repeated with TR values ranging from 1000
ms to 5000 ms on gray matter (GM), white matter (WM), and cerebrospinal fluid (CSF)
because they are different in T1.
Ten subjects were
taken from the Human Connectome Project (HCP) 10, which contains DWI data. Only 1 volume of non-DWIs (b = 0 s/mm2)
and 1 direction of DWIs (b = 1000 s/mm2) of each subject were
extracted for training. Images of 6, 3, and 1 subjects were used for training, validation,
and test, respectively. Each volume contained 140 slices, which were divided
into 7 x 2 (MB factor) = 14 slabs.
By multiplying the reference images with the
simulated slab profiles at different TRs (TR = 1000, 1500, 2000, 3000, 4000,
5000 ms), and then creating inter-slab aliasing on the simultaneously excited
slabs (Fig. 2b), images with different levels of boundary artifacts were
created. For GM, WM, and CSF, corresponding slab profiles were used. The tissue
segmentation was finished using FAST from the FMRIB software library (FSL)11. To imitate the SNR which decreases as the TR is
shortened, Gaussian white noise was added to reach a maximum level of 10 dB
at TR = 1000 ms.
The convolutional network used in this study was a modification of U-net12, a network widely used for image segmentation. Its depth was
reduced to 3 and only 8 filters were used in the first layer of the network.
The model was trained by Adam optimizer13 with the structural similarity index (SSIM) loss14.
The training set
and validation set contained synthetic images at all TRs except for TR = 1000
ms, which served as the test data. The images with artifacts and the slab
profiles were used as input, and reference images were used as output. For
further evaluation of the results, fractional anisotropy (FA) maps were
calculated using FDT from FSL11. The NPEN algorithm refined for the SMSlab acquisition1,8 was used for comparison in this study.Results and Discussion
Fig. 1 shows the
results of the Bloch simulation. As TR decreases, the magnitude decreases
because of insufficient T1 recovery. Slab crosstalk leads to intensity
reduction at the edges of slabs. The slab profiles vary for different kinds of
tissue. The longitudinal magnetization of tissue with shorter T1 (WM) is
recovered better.
The synthetic
artifacts are shown in Fig. 2a. Image contrast changes between different TRs. Intensity
inhomogeneity at slab boundaries becomes more severe and SNR drops when TR is shortened.
In DWIs, the SNR is lower, but the artifacts are less severe because the signal
of CSF is suppressed. Fig. 2b shows the aliasing pattern of the SMSlab
acquisition.
Fig.3 and Fig. 4
compare the results of the proposed method with NPEN. We can hardly see boundary artifacts in
the images corrected by CNN, while residual artifacts are still visible in the
results of NPEN. Moreover, CNN shows a strong suppression of noise, which
provides a better vision of small fibers in the FA maps. NPEN has little
resistance to noise, which leads to FA maps with low-quality.Conclusion
From the
results, we may draw a conclusion that the CNN-based method outperforms NPEN in
boundary artifacts correction. It is noteworthy that the iterative NPEN method
needs hours for computation of a whole-brain volume, which is impractical when a
large amount of DWI volumes are acquired, while it takes a trained CNN model less
than 1 second for it. Therefore, the CNN-based method is promising for boundary
artifacts correction for the SMSlab acquisition. This study serves as a preliminary
experiment for this idea. Ground truth data and real artifacts will be acquired
for training in the next step.Acknowledgements
No acknowledgement found.References
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