Michael J van Rijssel1, Frank Zijlstra1, Peter R Seevinck1, Peter R Luijten1, Dennis W J Klomp1, and Josien P W Pluim1,2
1Center for Image Sciences, UMC Utrecht, Utrecht, Netherlands, 2Department of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, Netherlands
Synopsis
Applications involving EPI readouts, such as
diffusion weighted imaging and functional imaging, are hampered by geometrical
distortions caused by static field inhomogeneities (ΔB0). Pixel
shift maps can be inferred from ΔB0 maps. Though it is common
practice to smooth these maps before calculating pixel shifts, doing so reduces
susceptibility-induced local ΔB0 variations. This study investigates
the importance of local ΔB0 changes in correctly predicting EPI
distortions. Preliminary data obtained from the human breast in-vivo shows that
susceptibility-induced changes in ΔB0 are essential in accurately
predicting EPI distortions.
Purpose
Echo
planar imaging (EPI) is currently the most common acceleration technique when
performing diffusion weighted (DWI) or functional imaging (fMRI). Images
recorded using EPI readouts are prone to several artefacts, most prominently
geometrical distortions caused by static field inhomogeneities (ΔB0).
Several correction methods are available that attempt to recover undistorted
images, both retrospectively and prospectively.1 When applying
retrospective correction using ΔB0 maps, whether estimated from a
multi-echo acquisition or from a reversed phase-encoded EPI acquisition, it is
common practice to ensure these maps are smooth by e.g. low-pass filtering,
polynomial fitting or kernel smoothing. This practice eliminates noise from ΔB0
maps, since noise can give rise to inconsistencies in the inferred displacement fields. It also reduces local ΔB0 variations induced by
susceptibility differences at tissue interfaces. This study investigates the
role of susceptibility-induced local variations in ΔB0 maps in the
prediction, and ultimately correction, of EPI distortions.Methods
A
healthy female volunteer (aged 27 years) underwent a breast MRI examination using
a unilateral breast coil setup on a 7T whole-body MR system (Achieva; Philips,
Cleveland, Ohio, USA). The protocol involved a gradient-echo Dixon acquisition
(1.5x1.5x1.5 mm3), a fat-suppressed spin-echo EPI (2x2x3 mm3, bandwidth/voxel 20 Hz) and a dual-echo ΔB0
measurement (2.5x2.5x2.5 mm3). In order to study global and local ΔB0
effects separately, the global ΔB0 variation was determined by
performing a 3rd-order polynomial fit to the measured map, while the
local variation was inferred from the Dixon acquisition. Based on the Dixon
in-phase, water and fat reconstructions, a 3D susceptibility model of the volunteer’s
breast was constructed, using tabulated values for air, water and fat.2, 3 From this model, local ΔB0 variation
can be predicted.4
For each of the maps (fitted global ΔB0, measured ΔB0, and
the fitted global + modelled local ΔB0) we simulated the EPI
distortions on the water reconstruction of the Dixon acquisition. The
simulation was performed with the FORECAST method, restricted to only
simulating distortions in the phase encoding direction (EPI direction).5 We compared each
of the simulated EPI images with the measured EPI acquisition, both visually
and quantitatively using the Pearson correlation coefficient (CC), to assess
the importance of local ΔB0 variations.Results
Figure 1
shows the original Dixon water reconstruction and the EPI image in the same
slice. Note that, in the EPI image, the deformation causes the glandular tissue
to appear as sheared and substantially compressed with respect to the
undistorted image. Figure 2 shows the composition of the breast model that was
used to simulate local susceptibility-induced ΔB0 effects. The right
panel indicates that local changes at tissue boundaries can be substantial,
especially compared to the global gradient caused by the tissue-air boundary. Figure 3 shows the
simulated EPI images for global, measured, and global + local ΔB0 distributions
respectively, with the measured EPI’s outline overlaid. Table 1 reports the CC
as a quantitative metric for distortion prediction accuracy.Discussion
The
results in Figure 3 demonstrate that it is not sufficient to use global ΔB0
variation to predict EPI distortions. Adding local susceptibility-induced
effects seems to aid substantially in achieving a better prediction of the
distortion; note the high agreement between the measured EPI’s outline and the
simulated image in panel d of Figure 3, and the increased CC in Table 1. Whether
inclusion of a model of susceptibility-induced ΔB0 effects improves
EPI distortion prediction with respect to using measured ΔB0 maps
should be confirmed in a larger in vivo study.
We are aware of the fact that it is questionable
whether it is desired or even feasible to acquire ΔB0 maps at a
sufficiently high resolution to capture local effects in a clinical setting,
since they require long scan times and tend to be noisy. However, deriving
local ΔB0 information from anatomical scans already present in
clinical protocols is generally achievable, e.g. by using susceptibility models
derived from anatomical scans as we've done here.
Though this
study focusses on prediction of EPI distortion, we feel our results are
relevant when designing distortion correction techniques. As we show local ΔB0
information is required to obtain reliable predictions, correction techniques
will most likely improve from incorporating this information. For accurate distortion
correction in EPI breast imaging, this would mean that including local ΔB0
variation induced by the susceptibility differences between fat and parenchymal
tissue, will be essential.
Conclusion
Preliminary
work shows that smoothing ΔB0 maps prior to using them for EPI
distortion correction can lead to substantial underestimation of the
deformation. Including local susceptibility-induced ΔB0 variation, inferred from anatomical scans, will
improve distortion correction algorithms.Acknowledgements
This
work is part of the IMDI research program with project number 104003019, which
is (partly) financed by the Netherlands Organization for Scientific Research
(NWO).References
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