Rasim Boyacioglu1 and Mark Griswold1
1Radiology, Case Western Reserve University, Cleveland, OH, United States
Synopsis
Magnetic Resonance Fingerprinting
with Quadratic RF Phase (MRFqRF) can simultaneously map T1, T2, T2* and
off-resonance. It has been shown that local field inhomogeneities due to
susceptibility is encoded in MRFqRF off-resonance maps. Here publicly available
standard QSM processing tools were used to analyze two high resolution 3D
MRFqRF datasets from 3T. Susceptibility contrast is revealed after phase
unwrapping, background removal and B1 correction. QSM preprocessed data was
further analyzed with two dipole kernel inversion algorithms. Susceptibility
encoding in MRF framework is novel and brings immediate additional value to MRI
exam.
Introduction
Multiple quantitative
tissue property maps can be obtained with Magnetic Resonance Fingerprinting1
(MRF). Recently MRF framework was extended to also map off-resonance and T2* in
2D2 and the first implementation for 3D was proposed3.
The MRF sequence is made sensitive to different off-resonance frequencies by
linearly sweeping the on-resonance band with a quadratic RF phase function
(MRFqRF). For T2* mapping, first the frequency dispersion (T2’) in a voxel is
simulated in the dictionary and then the match is combined with T2. Off-resonance
maps have high anatomical contrast with minimal wrapping around the air-tissue
interfaces. Because the off-resonance encoding is based largely on the time
axis, we have seen that the off-resonance maps are less sensitive to Gaussian
noise. Simulations of repeated reconstructions with added noise show ~0.05 Hz
sensitivity for off-resonance (Figure 1). Based on the stability and available
anatomical contrast of MRFqRF off-resonance maps, it is suggested in this
abstract that they can be used for quantitative susceptibility mapping (QSM)
with the possibility to overcome some of the error-prone steps of QSM. Two high
resolution MRFqRF datasets are processed with online available QSM processing software
and results are presented.Methods
Two sets of MRFqRF data were
acquired with the flip angle, repetition time and RF phase replicated from 3D
MRFqRF3 with two different resolutions and orientations on a 3T
system (Siemens Skyra). Informed consent with IRB approval was obtained from
both volunteers. Dataset 1 acquired in 11 min: 300x300x144 mm3 FOV,
48 axial slices with 1.2x1.2x3 mm3 interpolated to 96 slices with
0.6x0.6x1.5 mm3. Dataset 2 acquired in 22 min: 300x300x154 mm3 FOV,
96 sagittal slices with 1.2x1.2x1.6 mm3 interpolated to 192 slices
with 0.8x0.8x0.8 mm3. Interpolation was done by zero-filling in
k-space for individual MRF image series before dictionary matching.
MRF images were reconstructed
after compression with randomized SVD4. Template matching was done
with a dictionary undersampled by 16 in the tissue property dimension.
Quadratic interpolation5 recovers the relative low resolution in the
tissue property dimension.
QSM analysis included Laplacian unwrapping with
STI Suite6, removal of background phase with Laplacian Background
Value7 (LBV), 3D polynomial fit to remove B1 effects, dipole kernel
estimation and two QSM inversions: truncated k-space division8 (TKD)
and closed-form L2 regularization9. QSM processing was done in
Matlab with the tools available from https://martinos.org/~berkin/1645_Bilgic.pdfResults
Figure 2 and 3 illustrate the
outputs from the individual stages of QSM processing pipeline starting from the
wrapped off-resonance maps to the final QSM maps from the two kernel inversion
algorithms. The output image from the QSM pre-processing (top row of Figure 2
and 3) has significant susceptibility contrast for both datasets. As expected,
TKD inversion brings more noise and less smoothing compared to closed-form L2
regularization.Discussion and Conclusions
In this work, it is demonstrated
that the local field inhomogeneity due to susceptibility is encoded in the MRFqRF
off-resonance maps. After the background removal, the susceptibility contrast
is revealed, even though it is not as sharp as typical contrast available from
7T. The through-time encoding of off-resonance and quadratic interpolation
after the template matching makes the off-resonance maps stable and precise,
which then makes QSM processing possible. Thus, inclusion of this simple QSM
processing provides one more contrast for MRFqRF.
It should be noted that the
relatively low standard deviation is not due to the coarse step size forcing the
signal evolutions to be matched on the same dictionary entry for repeated
reconstructions. Quadratic interpolation after matching with low resolution
dictionary brings the high resolution back and ensures an accurate match.
There are remaining issues to be
resolved such as the wraps in the frontal regions due to strong gradients from
the air tissue interfaces. These could be mitigated with a short TR
implementation of MRFqRF which would widen the on-resonance band. It should be
noted that B1 correction partially helps with frontal lobe inhomogeneity
especially for the axial acquisition.
This is the first example of simple
QSM processing of MRF data at 3T, bringing immediate additional value for MRF
acquisition. It is essentially for free and comes alongside with perfectly co-registered
T1/T2/T2*/off-resonance maps. With an optimized acquisition it could even be
considered as an alternative to standard QSM since one can bypass the
error-prone unwrapping step from the analysis pipeline.Acknowledgements
This work is supported by Siemens Healthcare.References
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