Yuichi Suzuki1, Katsutoshi Murata2, Hideyuki Iwanaga1, and Osamu Abe1
1Radiology Center, The University of Tokyo Hospital, Tokyo, Japan, 2Siemens Healthineers, Tokyo, Japan
Synopsis
Keywords: Data Acquisition, Diffusion/other diffusion imaging techniques
We examined the application order of MPG pulses (called
reordered MPG) that can uniformly collect spatial diffusion information even if the
examination is interrupted, compare it with the an electrostatic repulsion method (conventional method, called
original MPG), and verify its usefulness. In conclusion, The reordered MPG, which was rearranged based on
the MPG direction of the original, could collect diffusion information more
uniformly than the original MPG even if the inspection examination
was interrupted.
Purpose
When
acquiring diffusion-weighted image (DWI) such as diffusion tensor imaging and
high angular resolution diffusion imaging (HARDI)1, an
electrostatic repulsion method (conventional method)2 is one of the
optimization methods of motion probing gradient (MPG) application direction.
This MPG application method is widely used not only in the research field but
also in clinical practice. Imaging time can be shortened using simultaneous
multislice3, etc., but imaging time tends to be longer with DSI4
and Q-ball imaging5. If the MRI examination
is interrupted in the middle, it cannot necessarily be said that
the data acquired by the conventional method are spatially uniform diffusion information.
Therefore, this study aimed to examine the application order of MPG pulses
(called reordered) that can uniformly collect spatial diffusion information
even if the examination is interrupted, compare it with the conventional method
(called original), and verify its usefulness.Materials and methods
The
study participants were 11 healthy men. DWI data used as reference were as
follows: repetition time/echo time, 9000/109 ms; slice, 60 sections; matrix,
96*96, field of view, 240*240 mm2; b-value, 3000 s/mm2;
MPG, 64 axes (plotted on a hemispherical surface), and data for 10.4 min of
imaging time. In these data, the order of the MPG application axes was
rearranged so that even if the scan was interrupted in the middle, the MPG
application order also changes so that data could be acquired uniformly in a
spatial and time-series manner. For these changes to occur, mathematical
induction with electrostatic potential energy (cost function) was used. First,
select the first axis of the conventional method. Then, from the remaining 63
axes, the one with the lowest potential energy was selected to determine the
second axis. Similarly, for a given P-axis, the one with the lowest potential
energy from the nonselected MPG (65-P) axes was adopted. We rearranged the
order of all 64 axes in this way. Using the Voronoi diagram {Fig.1(a)}, the
time-series variation of the area distribution on the sphere and the standard
deviation of the Voronoi area on each MPG axis were obtained for the reordered
and the original. We compared the potential energy ratio (PER). PER is the
ratio of the potential energy when applying n-axis by the reordered and the
potential energy of MPG optimized by the n-axis electronic repulsion method. Assuming
that the scan was interrupted in 50% (32 axes) and 75% (48 axes) of the
examination, we calculated the Fiber orientation distribution (FOD)6 and
Orientation distribution function (ODF)4,5 by the original and the
reorder, respectively, and calculated the similarity of the reference data to
the FOD and ODF. MRtrix3 was used for FOD calculations, and the diffusion
toolkit was used for ODF calculations. Similarity was calculated using Jensen-Shannon
Divergence (JSD)6 for FOD and angular correlation coefficient (ACC)6 for ODF, and the region of interest was only the segmented white
matter with 3D T1 weighted image. Wilcoxon’s signed-rank test was performed on
the obtained results (p < 0.05).Results
The
standard deviation of the Voronoi area was lower in the reordered than in the
original in all application axes {Figs.1(b) and Fig.2}. The PER of the reordered was
lower than that of the original in all the applied axes (Fig.3). The average
JSD values were 0.00010629 for the original MPG 32 axes, 0.00007044 for the reordered
32 axes, 0.00003688 for the original 48 axes, and 0.00002295 for the reordered
48 axes. A significant difference was found between the original and reordered
for both 32 axes and 48 axes (p = 0.0033) {Fig.4(a), (b) and Fig.5(a)}. The
average ACC values were 0.95061 for the original MPG 32 axes, 0.95632 for the reordered
32 axes, 0.974489 for the original 48 axes, and 0.978542 for the reordered 48
axes. A significant difference was found between the original and reordered for
the 32 axes and 48 axes (p = 0.0033) (Fig. 4(c), (d) and Fig.5(b)).Disscussion
The usefulness of the reordered MPG was suggested
from the results of Voronoi cells and the comparison of JSD and ACC using
actual DWI data. However, in this study, the MPG had 64 axes, and the
interruption assumption was only two, i.e., 32 axes and 48 axes. Thus, future
examinations under other conditions are necessary. Furthermore, verification in
patients with brain disorders and neonate or pediatric are necessary.Conclusion
The
reordered MPG, which was rearranged based on the MPG direction of the original,
could collect diffusion information more uniformly than the original MPG even
if the examination was
interrupted.Acknowledgements
This work was supported by KAKENHIοΌ20K08016οΌ in
JAPAN.References
1
David
S Tuch, Timothy G Reese, Mette R Wiegell, et al. High angular resolution
diffusion imaging reveals intravoxel white matter fiber heterogeneity. Magn
Reson Med. 2002 Oct;48(4):577-82.
2
D
K Jones, M A Horsfield, A Simmons. Optimal strategies for measuring diffusion
in anisotropic systems by magnetic resonance imaging. Magn Reson Med. 1999
Sep;42(3):515-25.
3
K
Setsompop, J Cohen-Adad, B A Gagoski, et al. Improving diffusion MRI using
simultaneous multi-slice echo planar imaging. Neuroimage. 2012 Oct
15;63(1):569-80.
4
V J Wedeen, R P Wang, J D Schmahmann, et al. Diffusion spectrum
magnetic resonance imaging (DSI) tractography of crossing fibers. Neuroimage.
2008 Jul 15;41(4):1267-77.
5
David
S Touch. Q-ball imaging. Magn Reson Med. 2004 Dec;52(6):1358-72.
6
Kurt
G Schilling, Vaibhav Janve, Yurui Gao. Histological validation of diffusion MRI
fiber orientation distributions and dispersion. Neuroimage. 2018 Jan
15;165:200-221.