Jiazheng Zhou1,2, Ali Aghaeifer1, Gisela Hagberg1,3, and Klaus Scheffler1,3
1High-Field Magnetic Resonance, Max Planck Institute of Biological Cybernetics, Tübingen, Germany, 2Graduate Training Centre of Neuroscience, IMPRS, University of Tübingen, Tübingen, Germany, 3Biomedical Magnetic Resonance, University Hospital Tübingen (UKT), Tübingen, Germany
Synopsis
We use a UTE sequence combining with Dixon method to obtain the subject specific
susceptibility distribution, with 4-class tissue segmentation. The susceptibility model was then used to simulate motion-induced B0
change for two head positions. A good agreement between the simulated and measured field map has been observe. A forward field map predicting strategy was explored using the susceptibility model.
Purpose:
Echo Planar Imaging (EPI) and balanced Stead-Stated Free Precession
(bSSFP) are frequently used pulse sequences in functional magnetic resonance imaging
(fMRI). The capability to acquiring the brain volume within seconds makes them a significant,
non-invasive tool for probing dynamic changes in the blood-oxygenation-level-dependent
(BOLD) response. Both sequences are sensitive to magnetic field (B0) inhomogeneity.
Perturbations in the field result in signal loss, banding artifact, and geometric
distortion.
Therefore, correcting
geometric distortions in functional images increases the accuracy of
co-registration to structural MR. Correcting distortion using acquired Field maps
has been shown to improve registration1. Subject movement can change the pattern of B0
inhomogeneity. However, it’s impractical to acquire a field map matches every possible movement during functional data acquisitions. Previously, field
probes have been used to estimate the dynamic of field fluctuation and correct
for this, but
they cannot fully estimate B0 inside the brain since they are placed outside
the brain.2
Here, we estimate the
motion-related B0 variations using a Fourier-based
dipole-approximation method3-5. A 4-class susceptibility model (air, bone, fat, and
water) is calculated using a combined ultrashort-echo-time/Dixon (UTE/Dixon)
MRI sequence.
Method:
A 3D UTE sequence with spiral trajectory was used after shimming
the entire volume with the scanner’s second-order spherical harmonic (SH) shim.
A dual-echo GRE sequence was used to measure reference B0 maps and scanner’s
background inhomogeneity. The detailed MR sequence parameters are listed in
Table 1.
A 4-classes
(air, bone, fat, and water) susceptibility model was implemented in MATLAB
(MathWorks) (Flow chart, Figure2). The air mask, including cavities, was
created using an empirically determined magnitude threshold6 of the first and
third echo as well as by morphologic filtering. The cortical bone was segmented
using inverse of the transverse effective relaxation rate (R2*) estimated from all
three echoes, where the cortical bone has high R2* values (R2*bone≥0.3ms-1)7. The bone structures were segmented using an
empirically determined threshold and cleaned up using morphologic filtering.
The remaining tissue was assigned a relative water-fat fraction, determined
through a two-point Dixon decomposition8 using the second (out-phase) and third
echo (in-phase). The water-fat fraction r is a normalized map9, ranging from
-1(purely fat) to +1 (purely water). Finally,
the susceptibility map of mix water and fat voxel was then calculated from the
relative water-fat fraction r using the linear mapping as follow:$$\chi_{water-fat map} = \frac{(1+r)}{2}\times\chi_{water-mean}+\frac{(1-r)}{2}\times\chi_{fat-mean}$$
Then,
the binary air and bone mask were applied to have the subject-specific
susceptibility model $$$(\chi_{water-mean}\approx-9.2ppm, \chi_{fat-mean}\approx-10ppm, \chi_{bone}\approx-11.3ppm, \chi_{air}\approx3.6ppm)$$$. A
Fourier-based method was then used to calculate the estimated field map from subject-specific susceptibility model for position 1.
Two
different head positions were measured to demonstrate field map predicting for
motion-induced B0 variations. The measurement was repeated with the head in a
second position without further shimming. For the second position, two
alternative strategies were used for predicting the field maps. 1) From the
measured position 1 field map using the position calculated transformation matrix (FSL10 FLIRT11 toolbox,
a
12-degree affine transformation) and tri-linear
interpolation. 2) From the susceptibility model using the transformation matrix
followed by a forward calculation of the expected field map.
Result:
Figure
3 shows the field maps estimated from the UTE susceptibility model for the first
position. Estimated field map has a similar deviation of inhomogeneity (σB0 = 26.9Hz)
in comparison to the measured one (σB0 = 24.2 Hz). Figure 4 shows the discrepancy between the estimated
field map and the measured field map for motion-induced B0 variations.
The
field map difference for strategy 1 was calculated between the measured position
2 field map and a field map co-registered from position 1. The difference of
the forward strategy 2 was calculated between the estimated field maps. The σB0
of the field map difference using the proposed method is 2.7Hz, compared to
10.6Hz of the measured field map.Discussion:
In this study, we further improved the UTE method to estimate the field map12, with 4-class tissue
segmentation. The σB0 of estimated and measured field map are in good agreement.
The
forward prediction strategy has a smoother difference field map, compared with
the measured strategy. The potential reasons would be 1) B0-variation induced
by the respiration cycle was not taken into consideration for forwarding strategy;
2) The tri-linear interpolation of the position 1 field map would smooth the
field map. In the future, the subject motion time series could
be captured using a motion camera. However, the motion camera only recorded the rigid
body motion from the skull. The relative motion between the skull and neck needs to
be further investigated.Acknowledgements
This work was supported by DFG SCHE658/13 and
the Max Planck Society.References
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