Yuan Le1, Jun Chen1, Phillip J. Rossman1, Armando Manduca1, Kevin J. Glaser1, Bradley D. Bolster Jr.2, Stephan Kannengiesser3, and Richard L. Ehman1
1Radiology, Mayo Clinic, Rochester, MN, United States, 2US MR R&D Collaboration, Siemens Medical Solutions Inc., Salt Lake City, UT, United States, 3MR Application Predevelopment, Siemens Healthcare GmbH, Erlangen, Germany
Synopsis
Keywords: Elastography, Elastography, Transient wave, multi-scale encoding
We demonstrate imaging of the propagation of transient waves using
multi-scale motion encoding gradient waveforms. Displacement values are calculated
using the inverse Haar transforms. We validated the results by comparison with
wave images obtained using standard MRE acquisition and processing. The
approach provides the ability to image broadband motion more efficiently and
accurately compared with previous methods and promises to be a useful approach
for biomechanical studies of traumatic brain injury.
Introduction
MR Elastography (MRE) has an
expanding clinical role, particularly for noninvasive diagnosis of liver
fibrosis1. New applications for
brain and cardiac imaging are also emerging. Standard MRE techniques acquire
images of propagating harmonic shear waves in a steady state2, 3. Several
repetitions are acquired, using a fixed motion encoding gradient (MEG) shape
and a varying phase relationship with the applied motion, so that a series of
images is acquired at different phases of the propagating wavefield. It is also
possible to image broadband or transient mechanical waves as they propagate
through organs4. This information is
useful, for instance, in biomechanical studies of the distribution of traumatic
brain lesions resulting from external mechanical transients. However, using
standard MRE methods it is necessary to carefully balance the bandwidth and the
sensitivity of the MEG and design proper deconvolution techniques for transient
applications5,
which is not always practical when the motion frequency range is unknown. We
have developed a more efficient approach for transient wave imaging6, using multiple scale
Haar wavelet-based motion encoding gradients to detect motion of a broader
bandwidth, such as in transient MRE4, 7-11. With
this technique a high motion sensitivity is achievable over a wide frequency
range, and the displacement can be reconstructed with a simple inverse Haar transform.
In this study, we validated the technique by comparison with results of the standard
transient MRE.Methods
Both multi-scale MRE and standard MRE research sequences
were based on a spin-echo EPI sequence and with 3D motion encoding. Data were
acquired at a 3T clinical scanner (MAGNETOM Skyra, Siemens Healthcare,
Erlangen, Germany) with a PVC gel phantom. Table 1 lists the imaging
parameters. The details of the multi-scale MRE sequence and displacement map
reconstruction were explained in our previous abstract6. Three scales of Haar
wavelet plus a scaling function were used for MEG in multi-scale MRE: the 36ms bipolar
MEG detected the difference in the DC value
between consecutive 18ms-windows. Cumulative sums of the acquired phase
difference were then used as scaling function elements. 18ms, 9ms and 4.5ms MEG were used for 3
wavelet scales. The MEG amplitude was 10, 10, 14.1 and 20mT/m, respectively.
Ten sampling windows were acquired so the total sampled time duration was
180ms.
Two types of transient motion waveforms were generated
using a pneumatic driver (Resoundant Inc., Rochester MN, USA) for this study:
(1) one cycle of a 90-Hz sinusoidal wave; and (2) ten cycles of 90-Hz
sinusoidal waves.
With multi-scale MRE, displacement was calculated at each
voxel. The calculated displacement was then convolved with the MEG profile used
in standard MRE. The result was a simulated standard MRE phase difference using
the calculated displacement as the ‘truth’. These simulated phase difference
values were then compared to the phase difference acquired with standard MRE.
Finally, a Fourier transforms were performed on the
displacement in the phase encoding direction both over the total time duration for the spectrum
analysis, and over every 100ms time intervals overlapped (0-100ms and 50-150ms)
for a spectrogram analysis.Results
An example of phase difference maps from multi-scale MRE is
displayed in Figure 1. The wave motion detected using the 4.5ms MEG has a
shorter wavelength than those detected using longer MEG, reflecting the
sensitivity to higher frequencies. The displacement at one example voxel
(yellow dot in Figure 2) was found to change in both amplitude and frequency
during the 180ms sampling window, with both one and ten 90Hz wave cycles. As
shown in Figure 3, the simulated phase differences were slightly higher with
both types of transient motion and all three motion directions, but the shapes
of the waveforms matched very well in general. The spectrum and the spectrogram
in Figure 4 shows that with the stimulation of only one 90Hz motion cycle, the
response was a broadband motion with a much lower peak frequency of around 40Hz;
while with ten 90Hz cycles, the response initially started with a lower
frequency (around 40Hz) but later reached 90Hz. Conclusions
The simulated phase difference from multi-scale MRE matched very well
with acquired phase difference of standard MRE, indicating that the multi-scale
MRE accurately detected any motion within the bandwidth of that standard MEG.
The simulated phase difference was slightly higher, which might be caused by
the different non-linearity in the MEG profile in the two methods. Spectrum
analysis showed a very realistic frequency response during the selected
time-window. These results indicate that multi-scale MRE is a promising
technique in applications such as tissue biomechanical studies related to
traumatic brain injury. Future studies include transient brain motion detection
in healthy volunteers.Acknowledgements
This work was supported by grant from National Institutes
of Health R01EB001981.References
- Yin, M., et al. Abdom Radiol (NY).
2018;43(7):1546-51. Epub 2017/10/11.
- Litwiller, D. V., et al. Curr Med
Imaging Rev. 2012;8(1):46-55.
- Muthupillai, R., et al. Science.
1995;269(5232):1854-7. Epub 1995/09/29.
- McCracken, P. J., et al. Magn Reson
Med. 2005;53(3):628-39. Epub 2005/02/22.
- Solanas, P. S., et al. Nmr in
Biomedicine. 2021;34(2).
- Le, Y., et al. Joint Annual Meeting ISMRM-ESMRMB; London,
England, UK.
- Souchon, R., et al. Magn Reson Med.
2008;60(4):871-81. Epub 2008/09/26.
- Hofstetter, L. W., et al. Magn Reson
Med. 2019;81(5):3153-67. Epub 2019/01/22.
- Hofstetter, L. W., et al. Phys Med
Biol. 2020. Epub 2020/12/23.
- Smith, D. R., et al. J Biomech Eng-T
Asme. 2020;142(7).
- Shahryari,
M., et al. Magnetic Resonance in Medicine. 2021;85(4):1962-73.