Ziyi Wang1, Mu He2, Elianna Bier3, Brian Soher4, Joseph Mammarappallil4, Sudarshan Rajagopal5, Yuh-Chin Huang6, and Bastiaan Driehuys1,3,4
1Biomedical Engineering, Duke University, Durham, NC, United States, 2Electrical and Computer Engineering, Duke University, Durham, NC, United States, 3Medical Physics Graduate Program, Duke University, Durham, NC, United States, 4Radiology, Duke University Medical Center, Durham, NC, United States, 5Division of Cardiology, Duke University Medical Center, Durham, NC, United States, 6Division of Pulmonary, Allergy and Critical Care, Duke University Medical Center, Durham, NC, United States
Synopsis
Hyperpolarized 129Xe is uniquely suited to imaging pulmonary
functions by virtue of its solubility and abundant chemical shifts. Previous
efforts established single-breath 3D imaging of 129Xe ventilation,
barrier uptake and RBC transfer at 1.5 Tesla. As MR vendors are increasingly transitioning
their multinuclear platforms to 3 Tesla, it becomes important to enable 129Xe
gas exchange MRI at higher field strengths. Here we demonstrate that by careful
measurement of spectral properties and optimization of RF and readout, short
T2* can be overcome, and 129Xe gas exchange MRI with quantitative
workflow is feasible and robust at 3 Tesla.
INTRODUCTION
Recently, hyperpolarized 129Xe, with its solubility and chemical shifts, has begun to be exploited for pulmonary gas exchange imaging. The first efforts used a multi-echo hierarchical IDEAL approach, 1 and subsequent work used interleaved 3D radial encoding of 129Xe in airspace and dissolved compartments combined with a single-echo 1-point Dixon approach 2 to decompose the barrier and red blood cell (RBC) compartments. To date, these techniques have only been implemented at 1.5 Tesla, due to the short T2* (~2ms) of 129Xe dissolved in alveolar septa. However, with MR vendors increasingly transitioning their multi-nuclear platforms to 3 Tesla, it is essential to establish that 129Xe gas exchange MRI is also feasible at higher fields. The objective of this work was to develop a 3-Tesla implementation for Dixon-based 129Xe gas exchange MRI and to determine optimal acquisition parameters.METHODS
The study enrolled 8 healthy subjects to optimize parameters, and obtained
representative images in 4 patients with alpha-1 antitrypsin deficiency (3 MZ
and 1 ZZ) and a COPD patient. All imaging was conducted on a 3T Siemens
MAGNETOM Trio (VB19). First, in vitro spectroscopy was used to identify the
minimum RF sinc pulse duration that could selectively excite dissolved-phase 129Xe
without gas-phase contamination. The resulting 0.69 ms 1-lobe pulse was then
used to acquire a calibration spectrum that was fit in the time domain to
determine the frequency and phase separation between the barrier and RBC
resonances, to calculate the TE of barrier and RBC being 90° out of phase. The TE90 and sinc pulse were used to acquire 1000 interleaved 3D-radial gas and
dissolved views, with flip-angles = 0.5/20°, TR = 7.5ms and FOV = 36cm3
(Figure 1). Each view had 64 points, acquired at 399Hz/pixel (2.5ms read-out). Each
readout gradient was carefully timed to ensure the first point was acquired at
k=0 and each was followed by an x-gradient crusher to dephase the gas-phase
residual magnetization. After image encoding, a singled dissolved-129Xe
spectrum was acquired to derive the global, steady-state RBC:Barrier ratio corresponding
to this flip angle and effective 15ms dissolved-phase TR. All imaging was done
with patients inhaling an effective 129Xe dose of ~110 ml. 3 The reconstructed dissolved-phase
image was phase-shifted to align RBC and barrier to real and imaginary channels
such that their intensity ratio matched the RBC:Barrier from the spectrum. The
images were processed as previously described. 4RESULTS
Figure 1(c)(d)
shows the consumption of gas and dissolved-phase magnetization over the
acquisition. Figure 2 shows the effect of tuning sinc pulse duration on
off-resonance gas-phase excitation. The optimum of 0.69ms generating a
tolerable 3% contamination in vivo. Figure 3 shows the chemical shift of the
dissolved-phase resonance for 2 representative healthy subjects as well as the line-shape
parameters of the healthy cohorts at 1.5 vs. 3 Tesla. At 3T (34.092MHz gas-phase), the RBC and barrier resonance are at 217.5 ± 0.5 ppm and 197.9 ± 0.2
ppm, with linewidths 8.5 ± 0.4 ppm and 7.7 ± 0.3 ppm respectively. The RBC linewidth
suggests a lower bound of T2* ~1.2ms. Figure 4 shows representative
reconstructed images of a patient with longitudinal scans at both 1.5T and 3T, 21 months apart. Figure 5 shows the processed color maps of the same patient. Both
images show mild ventilation defects and enhanced barrier uptake, but most
notably, a prominent RBC transfer defect is visualized on both images.DISCUSSION
These preliminary results indicate that 1-point Dixon-based imaging of 129Xe
gas exchange is feasible at 3-Tesla. Selective excitation of dissolved-phase 129Xe
benefits from the larger chemical shift and was enabled with a simple 0.69ms
1-lobe sinc pulse. This enabled k = 0 to be acquired at roughly TE = 0.45ms
where RBC and barrier are 90° out of phase. Analysis of the dissolved line-shapes
suggests T2* ~1.2ms, which was managed with a 2.5ms read-out. Despite the short
T2* of the dissolved resonances, the gas-phase resonance T2* was estimated to
be ~8ms, making it important to crush its transverse magnetization. This work
incorporated several improvements to the initial published method. 4 First, the spectrum for determining the RBC:Barrier ratio was now acquired as part of the
imaging sequence, ensuring it reflected the steady-state conditions as the
image. Secondly, the radial view randomization ensures that the sequence is
robust against potential early exhalation by patients with compromised pulmonary function. Initial estimates suggest that image SNR is comparable to 1.5 Tesla,
while several aspects remain to be further optimized. Based on these
preliminary results, it appears that 129Xe gas exchange imaging can
be deployed to high field clinical scanners. Acknowledgements
R01HL126771,
R01HL105643, P41 EB015897, Gilead Sciences, Duke MITPReferences
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