Zheng Zhong1,2, Kaibao Sun2, Guangyu Dan1,2, Muge Karaman1,2, and Xiaohong Joe Zhou1,2,3,4
1Bioengineering, University of Illinois at Chicago, Chicago, IL, United States, 2CMRR, University of Illinois at Chicago, Chicago, IL, United States, 3Radiology, University of Illinois at Chicago, Chicago, IL, United States, 4Neurosurgery, University of Illinois at Chicago, Chicago, IL, United States
Synopsis
Sub-millisecond Periodic Event
Encoded Dynamic Imaging or SPEEDI (also known as SMILE) has been reported
to be capable of achieving sub-millisecond temporal resolution. However, the total
scan times of this technique is typically very long. In this study, we have
incorporated two techniques – reduced field of view (rFOV) and echo-train acquisition – into a
SPEEDI sequence to substantially reduce the total scan times. This
sequence, which we call re-SPEEDI, has been demonstrated in phantom experiments
for capturing rapidly changing currents in a wire loop with a temporal
resolution of 0.6ms-0.8ms.
Introduction
A recently reported technique – Sub-millisecond
Periodic Event Encoded Dynamic Imaging or SPEEDI (also known as SMILE1,2) – has demonstrated sub-millisecond
temporal resolution in MRI using an FID or spin-echo acquisition. However, the total
scan time is long, which prevents SPEEDI from being practically used in a wide
range of potential applications. Decreasing the matrix size can reduce the scan
times, but compromises the spatial resolution. One possible approach is to
simultaneously reduce the field-of-view (FOV) by focusing on a region of
interest3–5 so that the spatial resolution can
be maintained. In addition, the scan times of SPEEDI can be further shortened by
replacing FID-based or spin-echo-based acquisition with echo-train-based
acquisition. In this study, we report a variation of the SPEEDI sequence, which
we call re-SPEEDI, by incorporating the two aforementioned strategies – reduced
FOV and echo-train acquisition.Methods
re-SPEEDI:
To
reduce the FOV, re-SPEEDI employed a 2D RF excitation pulse, which was designed
by tilting
2D excitation k-space3,4. To
incorporate echo-train acquisition so that frequency-encoding can be applied
along one spatial direction to reduce the scan time, an FID signal in the
original SPEEDI sequence was replaced with a non-phase-encoded gradient-echo
train (Fig. 1). Each echo in the echo train was positioned in an individual
k-space raster, and all echoes in the echo train were spread across a series of
time-resolved k-space rasters (k-space 1, k-space 2, … k-space
n), as shown in Fig. 1. This process was repeated with different phase-encoding
values until all 2D k-space rasters were adequately sampled. After a 2D Fourier
transform, a collection of time-resolved images was obtained with a temporal
resolution determined by echo spacing (esp). Compared to SPEEDI, re-SPEEDI
considerably reduces the total scan times because of a smaller matrix size and
the use of frequency-encoded echo train signals.
Data
Acquisition:
A re-SPEEDI sequence (Fig. 1) was implemented on
a 3T GE MR750 scanner. Experimental demonstration was carried out using a
phantom that contained a rectangular wire loop submerged in water. A pulse generator was used to supply a rapidly
time-varying current to the wire loop, which was synchronized with the RF
unblanking signal from the scanner. The same signal was also used to trigger
the re-SPEEDI sequence in order to capture the dynamics of the phase change
produced by the time-varying current. The experiments were performed three
times, each with a different FOV: (a) full FOV that covered the entire phantom
(FOV=12cm×12cm, matrix=64×64, scan time=2:08, esp=0.6ms), (b) a reduced FOV in
the phase-encoding direction only (FOV=12cm×3cm, matrix=64×16, scan time=32s,
esp=0.6ms), and (c) reduced FOV in both frequency-encoding and phase-encoding
directions (FOV=4cm×4cm, matrix=32×32, scan time=1:04, esp=0.8ms). For each experiment,
a scan was first performed without current in the wire loop to establish a
reference, followed by another scan after applying a 3mA peak current with a
duration of 35ms and a shape that imitated an action potential. The other
acquisition parameters were: TR=2000ms, TE=2.8ms, and slice thickness=5mm.
Image
Analysis:
After
acquisition of time-resolved images using re-SPEEDI, the phase maps of these
images were produced at each time point. The phase evolution from a specific
point in the water phantom was extracted and compared with the simulated phase
change calculated using the following equation: $$\phi(t)=\gamma\int_{0}^{t}
B(t^{'})dt^{'}, [1]$$ where B(t) is the magnetic field produced by
the time-varying current in the wire loop.Results
The
dipole pattern produced by the current can be clearly seen on the phase maps
from all three experiments, as shown in Figs. 2-4, respectively. The
fast-changing phase evolution was captured with a 0.6ms or 0.8ms temporal
resolution, and agreed well with the simulation results using Eq. [1]. Compared
to conventional SPEEDI, the scan times were shortened by a factor of 4, 16, and
8 in the three experiments, respectively. In addition, the approach with
reduced FOV in both in-plane directions improved the spatial resolution from 1.8×1.8mm2 in full
FOV to 1.2×1.2mm2.Discussion and Conclusion
We have demonstrated the ability of re-SPEEDI
for substantially reducing the overall scan times while offering
sub-millisecond temporal resolution for capturing the dynamic current change in
a wire loop. The rFOV approach, which has been used to decrease the acquisition
times in previous studies6–8, was successfully incorporated into
SPEEDI. Imaging with an rFOV can also improve the spatial resolution without suffering
from aliasing artifacts. The echo-train acquisition method was a variable
alternative to the FID-based acquisition and balanced the conflicting
requirements between the total scan time and the temporal resolution. By
combining rFOV and echo-train acquisition, re-SPEEDI is expected to be an
important contributor to broadening the applications based on SPEEDI-type
sequences.Acknowledgements
This work was supported in part by NIH 1S10RR028898.References
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