Deep learning-based whole-brain B(1)(+)-mapping at 7T
Authors
- F. Krueger
- C.S. Aigner
- M. Lutz
- L.T. Riemann
- K. Degenhardt
- K. Hadjikiriakos
- F.F. Zimmermann
- K. Hammernik
- J. Schulz-Menger
- T. Schaeffter
- S. Schmitter
Journal
- Magnetic Resonance in Medicine
Citation
- Magn Reson Med 93 (4): 1700-1711
Abstract
PURPOSE: This study investigates the feasibility of using complex-valued neural networks (NNs) to estimate quantitative transmit magnetic RF field (B(1)(+)) maps from multi-slice localizer scans with different slice orientations in the human head at 7T, aiming to accelerate subject-specific B(1)(+)-calibration using parallel transmission (pTx). METHODS: Datasets containing channel-wise B(1)(+)-maps and corresponding multi-slice localizers were acquired in axial, sagittal, and coronal orientation in 15 healthy subjects utilizing an eight-channel pTx transceiver head coil. Training included five-fold cross-validation for four network configurations: NN(tra)(cx) used transversal, NN(sag)(cx) sagittal, NN(cor)(cx) coronal data, and NN(all)(cx) was trained on all slice orientations. The resulting maps were compared to B(1)(+)-reference scans using different quality metrics. The proposed network was applied in-vivo at 7T in two unseen test subjects using dynamic kt-point pulses. RESULTS: Predicted B(1)(+)-maps demonstrated a high similarity with measured B(1)(+)-maps across multiple orientations. The estimation matched the reference with a mean relative error in the magnitude of (2.70 ± 2.86)% and mean absolute phase difference of (6.70 ± 1.99)° for transversal, (1.82 ± 0.69)% and (4.25 ± 1.62)° for sagittal (NN(sag)(cx)), as well as (1.33 ± 0.27)% and (2.66 ± 0.60)° for coronal slices (NN(cor)(cx)) considering brain tissue. NN(all)(cx) trained on all orientations enables a robust prediction of B(1)(+)-maps across different orientations. Achieving a homogenous excitation over the whole brain for an in-vivo application displayed the approach's feasibility. CONCLUSION: This study demonstrates the feasibility of utilizing complex-valued NNs to estimate multi-slice B(1)(+)-maps in different slice orientations from localizer scans in the human brain at 7T.