Yang Zhao1, Yishi Wang2, Guangbin Wang1, and Weibo Chen2
1Department of Radiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China, 2Philips Healthcare, Beijing, China
Synopsis
Keywords: Data Acquisition, Data Acquisition, compressed sensing
The magnetization-prepared 2 rapid
acquisition gradient echo (MP2RAGE) sequence provides morphological
T1-weighted images and quantitative T1 maps. Compressed sensing (CS)
acceleration technique has been drawing extensive attention with its
high acquisition efficiency for MRI sequence. In this study, volume measurement
and ROI analysis were used to assess the images
obtained from CS-MP2RAGE sequence under different acceleration factors. We find
that CS-MP2RAGE show high similarity in brain structure volumes measurement and
ROI analysis with traditional SENSE-MP2RAGE. Those findings prove that
CS-MP2RAGE can be considered as an alternative to the SENSE-MP2RAGE, though the
specific acceleration factor still needs to be further studied.
INTRODUCTION
Morphological T1-weighted images are necessary for MRI applications, especially
as an anatomical reference in neuroimaging studies.1 MPRAGE(magnetization
prepared rapid gradient echo)is a commonly used sequence
to acquire 3D T1-weighted image, which has been used in the Alzheimer's Disease
Neuroimaging Initiative (ADNI) with high resolution. 2-3 However, the inhomogeneity of the transmit
B1 + and receive B1 – fields could affect the image
quality in high magnetic fields.
As an extension of the MPRAGE sequence,The magnetization-prepared 2 rapid
acquisition gradient echo (MP2RAGE) sequence could provide superior grey-white
matter contrast T1-weighted images and quantitative T1 maps. 4 A typical MP2RAGE scan with SENSE /GRAPPA
usually takes a long time.
In recent years,
compressed sensing (CS) acceleration technique has been
drawing extensive attention with its high acquisition efficiency for MRI
sequence5. Mussard6
accelerated MP2RAGE sequence using CS, and the obtained images were
considered equivalent to the gold standard GRAPPA-MP2RAGE, while shortening the
acquisition time by 57%.
In our research, we apply various acceleration
factors to all the volunteers and aimed to quantitatively assess the images obtained from CS-MP2RAGE sequence under
different acceleration factors compared to traditional
SENSE-MP2RAGE.METHODS
12 healthy volunteers were included who
underwent MRI scan on a 3T scanner (Ingenia CX, Philips, Best, The
Netherlands), using a 32-channel receive head coil. Four MP2RAGE sequences were
performed for each subject and the scan parameters are listed in Table1.
Firstly, volume
measurements obtained from CAT12 and VolBrain were assessed. Segmentation
of brain white matter (WM), gray matter (GM), and cerebrospinal fluid (CSF) was
performed using Computational Anatomy Toolbox (CAT12version 1613; http://www.neuro.uni-jena.de/cat/).
To evaluate subcortical structures, the online platform VolBrain software was
used (https://www.volbrain.upv .es). The segmentation results obtained from all
four sequence were compared using one-way ANOVA (P < 0.05 was considered significant).
Then, the following substructures were selected
for region-of-interest (ROI) analysis: putamen, thalamus, globus pallidus, caudate head, genu
of corpus callosum. We chose the genu of corpus
callosum as the reference WM to quantify the gray/white contrast. At these ROIs,
Contrast ratios (CRs) between structures
were calculated using the same equations as in Okubo et al7.
T1 values were also calculated using the
ROIs as just described. The mean T1 of a structure was measured as the average of the T1
values of each voxel within the region of interest. One-way ANOVAs were also used to assess CRs 7and
T1 value among all four sequences.RESULTS
The scan time was reduced by 43%, 71% and 81%
when CS acceleration factors was 5, 10 and 15 respectively, compared to 7
minutes for SENSE3,
The mean and SD of the volumes of WM, GM,
CSF, putamen, thalamus, globus pallidus, caudate on
the 12 participants are shown in Figure1. No significant difference in volumes
was observed among the four sequences.
The CRs of all sequences are shown in the
boxplots in Figure2. For most regions, CS-MP2RAGE images exhibited a lower CRs compared to the SENSE images, but there was no significant difference in CRs
for all sequences.
The measured T1 values of five ROIs are
displayed in FIGURE3. Although there is a trend that higher acceleration factors
lead to higher T1 values, it is not statistically significant.DISCUSSION
Our study is the first one to systematically
evaluate the differences in volume and image quality of brain structures
between the traditional SENSE-MPRAGE and CS-MP2RAGE with different acceleration parameters.Indeed, Mussard et al6 only compared the parallel imaging accelerated MP2RAGE and CS-MP2RAGE with single factor.
FIGURE4. shows that the overall image
quality allows distinguishing the main structures, even when CS=15. However, an
increased blurring comes with higher factor and impairs the reading of precise
structures such as in cerebellum or at GM–WM borders.6
Two commonly-used softwares were used here to segment the brain structures from the MP2RAGE images,CAT12 was used to segment WM, GM, CSF, and Volbrain was used to assess subcortical regions. As shown in the results, the increasing
factor dose not influence both tissue segmentations and ROI analysis. The
volumes of brain tissues and ROI analysis of healthy volunteers were compared between SENSE-MP2RAGE and CS-MP2RAGE. As
already demonstrated, in terms of volume, CRs and T1 value, there was no
statistical difference among all four sequences.
In future research, we plan to add other
methods to evaluate the results, such as DICE coefficient and Coefficients of
variation.CONCLUSION
CS-MP2RAGE shows
high similarity in brain structure volumes measurement and ROI analysis with
SENSE-MP2RAGE, even when
CS=15 (the scan time is 1:20 minutes, compared to 7 minutes for the SENSE3 gold
standard, a reduction of 81%).
Consequently, CS-MP2RAGE can be considered as an
alternative to the SENSE-MP2RAGE, though the specific acceleration factor still
needs to be further studied.Acknowledgements
No acknowledgement found.References
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