Tian Li1, Di Cui2, Ge Ren1, Edward S. Hui3, and Jing Cai1
1Department of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong, Hong Kong, 2Department of Diagnostic Radiology, The University of Hong Kong, Hong Kong, Hong Kong, 3Department of Rehabilitation Science, The Hong Kong Polytechnic University, Hong Kong, Hong Kong
Synopsis
Magnetic resonance fingerprinting (MRF) is an imaging technique
that effectively samples the transient state signal to achieve the goal of fast
multi-parameter measurement. However, the applications of MRF only focus on
static images, mostly brain image. Therefore, this study aims to investigate
the feasibility of different acquisition schemes of four-dimensional magnetic
resonance fingerprinting (4D-MRF) by computer simulation.
Synopsis
Magnetic resonance fingerprinting (MRF) is an imaging technique
that effectively samples the transient state signal to achieve the goal of fast
multi-parameter measurement. However, the applications of MRF only focus on
static images, mostly brain image. Therefore, this study aims to investigate
the feasibility of different acquisition schemes of four-dimensional magnetic
resonance fingerprinting (4D-MRF) by computer simulation.Introduction
Recently, quantitative magnetic resonance
imaging (MRI) technique has drawn increasing attention including magnetic
resonance fingerprinting (MRF),1 magnetic resonance
image compilation (MAGIC),2 and magnetic
resonance spin tomography in time-domain (MR-STAT).3 Among these
quantitative techniques, MRF has been investigated intensively since its first
introduction in 2013.1 It is an imaging technique that effectively samples the
transient state signal to achieve the goal of fast multi-parameter measurement.
However, the applications of
MRF only focus on static images, mostly brain image. Therefore, this study aims
to investigate the feasibility and different acquisition methods of four-dimensional
magnetic resonance fingerprinting (4D-MRF) by computer simulation.Method
The simulation of MRF
data acquisition and reconstruction were performed in Matlab (MathWorks,
Natick, MA) using in-house developed programs. The simulated MRF technique
consists of a IR-FISP MRF sequence with spiral trajectory acquisition. In
total, one thousand time points were simulated with 12 ms TR for dictionary
matching. For each slice, phase-sorting method was used to re-bin the acquired
data into 10 phases. The 4D-MRF were generated by simulating the images slice
by slice and then combined to form 3D volume. In order to study the influence
of the number of repetitions used for dictionary matching on the image quality,
MRF images were simulated with different number of repetitions from 1 to 15 and
the simulation was repeated 200 times for each number of repetitions. Extended
cardiac-torso (XCAT) phantom is a highly detailed whole-body numerical phantom
and it was used in this study. Abdominal T1, T2, and proton density (PD) maps
were generated using the XCAT phantom with irregular breathing patterns for MRF
simulation. The maximum diaphragm motion was set to 2 cm in cranial-caudal (CC)
direction and 1.2 cm in anterior-posterior (AP) direction. The diameter of the
tumor embedded in liver was 30 mm. Voxel size was 1.67 isotropic. Three
different methods were used to generate 4D-MRF images: 1) continuous
acquisition without delay between MRF repetitions; 2) continuous acquisition
with 5 seconds delay between MRF repetitions; 3) triggered acquisition with variable
delay between MRF repetitions to allow the next acquisition to start at
different respiration phase. After the generation of 4D-MRF images, the image
quality indexes, including absolute T1 and T2 value error, signal to noise
ratio (SNR), and tumor contrast were used to evaluate the reconstructed images
with different repetitions. The absolute T1 and T2 value were compared with the
ground truth values from XCAT phantom images.Results
Dynamic MR parametric maps using three different acquisition
methods were successfully estimated from both XCAT phantom. An example of
simulated 4D-MRF images is shown in Figure 1. The overall and liver T1 value
error, liver SNR in T1 and T2 maps, and tumor SNR from T1 maps from triggered
method is significantly different compared to the other two methods (p-value
< 0.05). The other image quality indexes have no significant difference between
the triggered method and the other two fixed-gap methods. All image quality
indexes exhibit no significant difference (p-value >0.05) between the
acquisition methods with 0 second and 5 seconds delay. The image quality
indexes measurement results are shown in Figure 2 to Figure 3. Discussion
We have successfully demonstrated the
feasibility of 4D-MRF technique and investigated three different acquisition
methods using computer simulation. Among three different acquisition methods, triggered
method showed better performance in terms of certain image quality indexes than
the other two methods while the other two methods showed no significant
difference between them. However, the 0s gap acquisition method can save around
17 mins for a 20 slices 4D-MRF acquisition compared to the other two methods
and the triggered method requires additional manual efforts. Further in vivo
studies are needed to determine the optimal acquisition method for clinical
practice.Conclusion
4D-MRF
technique was investigated using three different acquisition methods in
computer simulation where the triggered method showed better performance than
the other two methods. The triggered method has been tested successfully in
healthy volunteers.Summary
We investigated
three different acquisition methods for 4D-MRI
technique in simulation study.Acknowledgements
This research was partly supported by
research grants (GRF 151022/19M and GRF 151021/18M).References
1. Ma
D, Gulani V, Seiberlich N, et al. Magnetic resonance fingerprinting. Nature. 2013;495(7440):187-192.
2. Tanenbaum LN, Tsiouris AJ, Johnson AN,
et al. Synthetic MRI for Clinical Neuroimaging: Results of the Magnetic
Resonance Image Compilation (MAGiC) Prospective, Multicenter, Multireader
Trial. AJNR Am J Neuroradiol. 2017;38(6):1103-1110.
3. Sbrizzi A, Heide OV, Cloos M, et al.
Fast quantitative MRI as a nonlinear tomography problem. Magn Reson Imaging. 2018;46:56-63.