Felix Krueger1, Christoph Stefan Aigner1, Max Lutz1, Layla Tabea Riemann1, Katja Degenhardt1, Bernd Ittermann1, Tobias Schaeffter1,2, Kerstin Hammernik3,4, and Sebasian Schmitter1,5,6
1Physikalisch-Technische Bundesanstalt, Berlin and Braunschweig, Germany, 2Division of Imaging Sciences and Biomedical Engineering, King's College London, London, United Kingdom, 3Technical University of Munich, Munich, Germany, 4Imperial College London, London, United Kingdom, 5Medical Physics in Radiology, German Cancer Research Center (DKFZ), Heidelberg, Germany, 6Center for Magnetic Resonance Research, University of Minnesota, Minneapolis, MN, United States
Synopsis
Keywords: RF Pulse Design & Fields, Parallel Transmit & Multiband
In
this work we utilize deep learning to estimate multi-slice whole-brain B
1+-maps
in sub-seconds from initial
localizer scans at 7T. The investigated
neural networks use the receive profiles of the individual coil elements of an
8Tx/8Rx transceiver head coil as input information. The networks are trained on
seven volunteers and tested in 2 unseen subjects for
transversal/coronal/sagittal slices by comparing the prediction with the
acquired B
1+-maps. Subsequently, the feasibility
of using the DL-based B
1+-maps in a subject-specific calibration
pipeline is demonstrated.
Purpose
Subject-tailored parallel transmit (pTx) pulses
for ultra-high fields (UHF) applications are typically calculated based on
subject-specific data of all transmit (Tx) channels, which requires additional
adjustment scans1. In the
human brain, transmit magnetic field (B1+) maps based
on pre-saturation acquisitions have been obtained in less than a minute with 8
Tx channels2. Yet, a higher resolution or an increase to 16 or 32 Tx
channels3,4 will lead to calibration times of several minutes. Particularly
for routine clinical scans, a fast, push-button, in-situ Tx field calibration
embedded in the scanner's adjustment routine is highly desired. Deep learning
(DL) based B1+-mapping techniques have shown promising
results in addressing this need and reducing calibration times5,6.
This
study investigates the feasibility of utilizing a recently presented DL-based
method applied to single slices in the heart6 for rapid, whole-brain
relative B1+-mapping at 7T. The B1+-maps are derived in sub-seconds from an
initial multi-slice localizer scan obtained in a CP+-like mode, typically acquired
for planning at the beginning of each scan session. Hence, the neural networks
(NNs) use the receive (Rx) profiles (B1-) of the individual
coil elements of an 8Tx/8Rx transceiver head-coil as input information. The NNs
are trained on seven volunteers and tested in two unseen subjects by
comparing DL-predictions with acquired B1+-maps
for different slice orientations.Methods
Multi-slice B1+-maps (8-10 slices, depending on anatomy) were measured in 9 subjects on a 7T whole-body
MRI system (Magnetom 7T, Siemens, Erlangen, Germany) with a custom-built 8Tx/8Rx
head-coil array7 utilizing a hybrid approach8. First a
small flip-angle 2D multi-slice GRE image (TR=100ms, TE=2.9ms,
resolution=2x2mm2, FOV=256x192mm2, slice
thickness=4mm, nominal FA=10°,
15 slices) is obtained with all Tx channels transmitting using a default shim
(i.e., the localizer). Then, the acquisition is repeated 8 times where only a
single Tx channel is active each. The latter scans are then merged with a 3D
actual flip-angle image (TR=75ms, TE=1.9ms,
resolution=2x2x4mm3, FOV=256x192mm2, slice
thickness=4mm, nominal
FA=60°) for all Tx coils active resulting in the ground truth (GT)
multi-slice B1+-maps.
The Rx-channel-wise localizer is split into real and imaginary parts and
stacked with the magnitude image along the channel dimension, forming the NN's input resulting in an input size of 128x96x17 per slice. Similarly, the GT Tx-channel-wise B1+-maps are split up into real and
imaginary data and arranged to a size of 128x96x16. Normalizing the input and output gives the originally absolute data a relative
nature. However, biases of relative methods (e.g., T1/proton density)9
are avoided by this procedure.
The investigated NNs are modified UNets10,4
with a symmetric loss11 function. The first NN (NNtra) was
trained on 66 transversal slices from seven volunteers and tested on 17
transversal slices from two unseen subjects. The second (NNcor) was
trained on 86 coronal and tested on 17 coronal slices, and the third (NNall)
was trained on 219 transversal/coronal/sagittal slices and tested on 51
transversal/sagittal/coronal slices.
The training parameters are as follows: ADAM
optimizer, learning rate=1*10-4, 2000 epochs, batch size=2. DL is performed on a 24 GB NVIDIA Titan RTX. The
predicted (PR) maps are qualitatively compared to the GT evaluated by the root mean squared error (RMSE)
and structural similarity index measure (SSIM). Static (phase-only)
and dynamic (4kT points) pTx optimization was subsequently performed on the DL-based
B1+-maps for different optimization targets.Results and Discussion
Fig.1 shows the magnitude and phase of the combined, multi-slice B1+-maps for the GT and PR by NNtra trained on multi-slice data in transversal orientation for
one unseen test subject. The maps reflect the default shim setting bdef (no
additional RF phases) resembling a CP+-mode. The
DL-based B1+-maps follow the GT for magnitude and phase (RMSE=0.053±0.010%). The match between PR compared to the GT B1+-maps is
further highlighted when looking at the channel-wise data for a
central slice (Fig.2). Fig.3 depicts the B1+-shimming results for the same example
slice after calculating a homogeneous shim vector bhom
and an efficiency setting beff. The latter is highly useful,
e.g., for subcutaneous fat saturation. The optimizations are based on the PR B1+-maps and
the resulting setting is applied to the PR and GT B1+-maps. The GT and PR maps always reflect
all features in the shimmed cases and for the default shim bdef .
The feasibility of using DL-based B1+-maps in a
subject-specific calibration pipeline is demonstrated by a quantitative
evaluation for the shim vectors bhom and beff
(Fig.3 (B)/(C)). This approach even provides good results for whole-brain dynamic pTx (4kt-points) excitation (Fig.3 (D)). Fig.4 shows the combined, multi-slice B1+-maps for four coronal slices for the GT and predicted
by NNtra, NNcor, and NNall. While NNtra
trained on transversal slices fails to predict coronal slices accurately, NNcor
and NNall successfully predict the combined maps. An evaluation of
the PR and the GT combined B1+-maps
is shown for coronal slices for all NNs (Fig.5 (A)/(B)) and for all
slice orientations predicted by NNall (Fig.5 (C)/(D)).Conclusion
Our results indicate
the feasibility of estimating complex, channel-wise, multi-slice B1+-maps
in the human head at 7T from a quick GRE localizer scan in multiple
orientations. Although we relied on relative B1+-maps due
to the normalization of the training data, an expansion to absolute data may be
feasible. Acknowledgements
We gratefully acknowledge funding from the
German Research Foundation (GRK2260-BIOQIC).References
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