Qingdang Qin1, Jiechao Wang1, Zhigang Wu2, Shuhui Cai1, and Congbo Cai1
1Department of Electronic Science, Xiamen University, Xiamen, China, 2MSC Clinical & Technical Solutions, Philips Healthcare, ShenZhen, China
Synopsis
Keywords: Quantitative Imaging, Quantitative Imaging
Compressed sensing (CS) relies on random under-sampling
measurements and has been the primary technique to accelerate quantitative parametric
mapping (QPM). The multiple
overlapping-echo detachment (MOLED) technique proposed recently is
a novel technique to realize quantitative parametric mapping in a single shot
within around 100 milliseconds. However, the two techniques still lack a
systematic comparison of acceleration performance in QPM. For the first time,
we analyze and compare the performance of these two techniques under the same conditions
via numerical experiments. The results show that MOLED outerperforms one-dimensional
under-sampling CS acceleration technique in T
2 quantification.
Introduction
Quantitative parametric mapping (QPM) has shown clinical value in diagnosis.1,2 However, long acquisition time is an essential obstacle to its application. Various acceleration methods have been proposed to improve the acquisition efficiency of QPM.3,4 As a recently proposed QPM acceleration method, multiple overlapping-echo detachment imaging (MOLED) proposed by our group can realize reliable QPM in a single shot.5-7 Different from traditional acceleration methods that are mainly based on under-sampling of k-space data and using prior information for reconstruction, MOLED accelerates QPM via increasing the collected information in a shot. However, the reconstruction performance of MOLED has not been thoroughly studied and analyzed. In this work, we took T2 mapping as an example to analyze and compare the reconstruction performance between MOLED and CS MRI based on a group of one-dimensional (1D) under-sampling patterns under the same experimental conditions.Methods
Imaging
sequences. Four imaging sequences were used: (1) MOLEDsequence;7
(2) SE-EPI sequence with a relatively high acquisition bandwidth to obtain a
minimum TE of 21.92 ms; (3) SE sequence; (4) partial Fourier transform SE-EPI (PFT-SE-EPI)
sequence with different partial Fourier acquisition schemes to ensure the same
TEs as MOLED. Four TEs (TE1 = 21.9 ms, TE2 = 51.9 ms, TE3=81.8
ms, TE4 = 110.7 ms) were used to obtain T2 maps for all
the sequences. The field of view (FOV) was 22 cm × 22 cm and the acquisition matrix
was 128 × 128. The parametric templates were from the public database IXI, and the simulated data were
synthesized by Bloch simulation on the parametric templates for the four
sequences. The numbers of simulated samples
used for training, validation, and testing were as follows: 5500, 300, and 600.
Numerical
experiments. Numerical human brains were utilized to compare the performances
of the different acceleration techniques. For CS MRI, each sequence needs to be
executed four times with different TEs to reconstructe a T2 map,
while MOLED only needs to be executed one time. For a fair comparison, the same
acceleration factor (R=4) ensures that the k-space data acquired by the three
sequences mentioned above for four TEs have the same amount of 128 phase-encoding
lines as the MOLED. The under-sampled SE and SE-EPI data were obtained by
retrospective under-sampling the fully-sampled SE and SE-EPI data through a
groups of 1D Cartesian variable density sampling patterns with R=4, while the
PFT-SE-EPI data were obtained by prospective sampling with a 1D uniform
sampling pattern with the same acceleration factor. Complex Gaussian noise was
added to the simulated data of above sequences.
Reconstructions. A
5-layer U-Net with skip connection structure8, which has been proven
to be highly efficient for the reconstruction of CS MRI and can
be used for the reconstruction of MOLED, was used to compare the performance of
different methods. In the reconstruction, all conditions remain the same except
for the number of input channels of the network (MOLED has one input channel,
while CS has four input channels). The loss function is l1 norm. Results
We only consider the range of T2 values of 20-150 ms to
rule out cerebrospinal fluid impact on reconstructed T2 maps. The
resulting T2 maps are shown in Figure 2. The MOLED can preserve more
tissue texture and is more accurate than CS-based methods for the noise-free
image. It also shows a better denoising ability for the noise contamination
data with noise level 2.5% (NL=2.5%). Table 1 lists the results of three
quantitative metrics: peak signal-to-noise ratio (PSNR), structural similarity index
(SSIM), and normalized root mean square error (nRMSE). All metrics indicate
that MOLED delivers better reconstruction results.Discussion and conclusion
The similarity between the reconstructed T2
maps of the different methods and the references is analyzed through numerical
experiments. The results show that in addition to the capability of achieving single-shot
T2 mapping, MOLED can get more accurate T2 values and
better-preseved tissue boundaries than 1D CS-MRI under the same acquired matrix
size and the same amount of data collected. This means that MOLED is also an
efficient means of acceleration of quantitative mapping, and deserves further
studies.Acknowledgements
This work was supported in
part by the Nation Natural Science Foundation of China under 82071913,
U1805261, 11775184, and 22161142024.References
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