Fan Yang1, Jian Zhang2, Guobin Li2, Jiayu Zhu2, Xin Tang1, and Chenxi Hu1
1Institute of Medical Imaging Technology, School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China, 2United Imaging Healthcare Co., Ltd, Shanghai, China
Synopsis
Three-dimensional
variable-flip-angle (VFA) T1 mapping is a valuable T1 quantification method
subject to a long scan time due to acquisition of multiple 3D images. SUPER (Shift
Undersampling improves Parametric-mapping Efficiency and Resolution) is a
recently developed method providing fast blockwise reconstruction for
accelerated parametric mapping. Here we develop a combination of SUPER and 3D CAIPIRINHA
to achieve 5-fold acceleration with 5 flip angles, validated with both
retrospective and prospective reconstruction. The results suggest that the
proposed method is highly accurate for accelerating 3D VFA T1 mapping, reducing
the whole-brain scan time from 6 to 1.5 minutes.
Introduction
Three-dimensional variable-flip-angle (VFA)
T1 mapping is a rapid T1 quantification method1-3 with
valuable clinical applications for brain4-6 and
liver7-10
imaging. However, long scan time is required to obtain multiple 3D images with
different flip angles. Parallel imaging with CAIPIRINHA11 is among the most common acceleration techniques for accelerating
3D imaging. SUPER (Shift Undersampling improves Parametric-mapping Efficiency
and Resolution)12 is a recently
developed model-based method, which provides fast blockwise reconstruction for
accelerated parametric mapping. We have previously developed SUPER-SENSE—a combination
of SUPER and 2D parallel imaging—for accelerating 3D VFA T1 mapping. The method
was validated with retrospective data only. Here we develop a combination of
SUPER and CAIPIRINHA to achieve higher acceleration rates, and we validate the
novel technique with both retrospective and prospective data. Methods
The combination of SUPER and CAIPIRINHA,
herein named SUPER-CAIPIRINHA, leverages both temporal and volumetric coil
sensitivity encoding to achieve a 5-fold acceleration rate within a scan of 5
flip angles. A 5-fold SUPER-CAIPIRINHA acceleration pipeline for VFA T1 mapping
is illustrated in Figure 1. In the first step, aliased images were generated by
performing Discrete Fourier Transform to k-space, which was undersampled by an
interleaved CAIPIRINHA sampling pattern. Of the 5-fold aliasing, 4-fold is
along the phase encoding direction and the other 1.25-fold is along the slice-encoding
direction. To reconstruct the unaliased parameter maps from the aliased images,
the blockwise curve-fitting cost function formulated based on the SUPER framework12 is minimized. Specifically,
the following cost function is minimized for each block:
∑m∑l |yml - wlr HSm∅l(x)|2
where yml represents value of the signal at the lth flip angle and the mth coil where l=0, 1, ..., L-1, and m=0, 1, ..., M-1, ∅l(x) represents the model evaluated at the lth flip angle defined by ∅l([M0,T1]T)=(M0 (1 - e-TR/T1 ) sinαl ) / (1 - e-TR/T1 cosαl) where x=[M0,T1]T is the parameters to estimate, TR is the repetition time, and αl is the lth flip angle, Sm represents the coil sensitivity of the mth coil, wlr=1/R·e(2πιlr/Ry) represents the modulating vector for each voxel in the block where r=0,1, ..., 7, R is the total acceleration rate, and Ry is the ky acceleration rate. We used
Levenberg-Marquardt for minimizing the above cost function.
Six healthy
subjects (age 23±1,
3 male) were imaged in a 3T scanner (uMR790, Shanghai United Imaging
Healthcare, Shanghai, China) after providing written informed consent. 3D T1-weighted
images were obtained using a 3D FLASH sequence with 24-channel head coil (17
used in acquisition). FOV was 300mm×300mm×150mm,
covering the entire cerebrum and image size was 192×192×30. Five flip angles were used namely 3°, 6°, 9°,
12°,
and 15°. Other sequence parameters were
slice-thickness/TR/TE/bandwidth =5mm/8ms/1.98ms/400Hz/Pixel. k-Space was
retrospectively undersampled based on SUPER-SENSE(R=4) and
SUPER-CAIPIRINHA(R=5). Retrospective data and prospective data were obtained and reconstructed separately. Gray matter and white matter were segmented based on the non-acceleration T1 map using a thresholding window of [1080 ms, 1580ms] and [580 ms, 1080 ms], respectively. Averaged gray matter and white matter T1 was compared between non-acceleration, SUPER-SENSE, and SUPER-CAIPIRINHA. Results
Figure 2 shows the reconstructed 3D T1/M0
maps of the entire cerebral cortex for 1 healthy subject. Image quality was
similar between non-acceleration, SUPER-SENSE, and SUPER-CAIPIRINHA and between retrospective and
prospective reconstruction. Figure 3 shows retrospectively accelerated T1/M0 maps,
fractional T1 difference maps and fractional M0 difference maps in the central
slice of 2 subjects. There was visible noise amplification due to acceleration
and SUPER-CAIPIRIRINHA was slightly noisier than SUPER-SENSE. Fine details of
each map were well-preserved for all methods and both subjects. Figure 4 shows the
comparison of retrospective and prospective acceleration in one subject. The quality
of the prospective data is consistent with that of the retrospective data,
despite slightly increased noise. Figure 5 shows the results of correlation analysis and Bland-Altman analysis for evaluating the consistency of ROI-averaged T1 quantification between non-acceleration, retro-SUPER-CAIPIRINHA, and pro-SUPER-CAIPIRINHA. The difference of both gray-matter and white-matter T1 between any pair of the 3 methods was not greater than 7ms, which is less than 1% of the average T1 of gray matter (1300ms, from non-acceleration) and white matter (868ms, from non-acceleration). SUPER-SENSE and SUPER-CAIPIRINHA reduced the scan
time from 6:11 minutes to 2:09 minutes and 1:29 minutes, respectively.Conclusions
In this work, we demonstrated a novel method to accelerate 3D VFA T1 mapping with a
5-fold acceleration rate by combining SUPER and CAIPIRINHA. The reconstructed
parametric maps had overall good image quality, accurate quantification, and
reasonable noise amplification. Prospective data was obtained and reconstructed
and showed consistent quality compared with retrospective data reconstruction. The
results show that SUPER-CAIPIRINHA is a feasible and accurate acceleration
method for 3D VFA T1 mapping. Acknowledgements
No acknowledgement found.References
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