Keywords: CEST / APT / NOE, Machine Learning/Artificial Intelligence, Synthetic Datasets
Motivation: The clinical application of CEST MRI is constrained by its relatively long scan time.
Goal(s): We aim to develop a deep learning reconstruction method for accelerating CEST imaging in the absence of true experimental data.
Approach: Here, we propose a model-based deep learning framework, in conjunction with the Channel-wise Attention mechanism and Total variation regularization, dubbed as MoDL-CAT. Moreover, we propose a new workflow to synthesize CEST data from the BraTS and fastMRI repositories.
Results: We demonstrate that the BraTS-CEST dataset can improve the performance of all deep learning networks tested, and the MoDL-CAT method achieves superior reconstruction quality to the state-of-the-art methods.
Impact: The proposed deep learning framework with channel-wise attention may offer a better prior for reconstruction. And our novel workflow to synthesize high-quality brain tumor CEST datasets might help researchers with limited data to explore various methods for accelerating CEST imaging.
National Natural Science Foundation of China: 81971605. Key R&D Program of Zhejiang Province: 2022C04031. Leading Innovation and Entrepreneurship Team of Zhejiang Province: 2020R01003. This work was supported by the MOE Frontier Science Center for Brain Science & Brain-Machine Integration, Zhejiang University.
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Fig. 1. Architecture of the proposed MoDL-CAT network. (a) The unfolded MoDL-CAT network, with trainable weights highlighted in red, in which the denoising block—Dw—shares weights across modules. (b) Each Dw block consists of an artifact estimator Nw and a residual connection. (c) The layout of each Channel-wise Attention convolutional (CA-conv) layer deployed in the artifact estimator Nw.
Fig. 2. Flowchart illustrating the synthesis of the BraTS-CEST dataset from the BraTS repository. Skull structures are reintroduced to brain tumor images of the BraTS dataset, and then the phase information and coil sensitivities from the fastMRI dataset are added to generate multi-coil k-space data. Subsequently, Z-spectra are imposed voxel-wise to create CEST contrast for different tissue types using Bloch-McConnell simulations.
Fig. 3. Comparison of true experimental data, and synthetic BraTS-CEST and fastMRI-CEST data. (a) CEST source images and their corresponding k-space maps. All images are normalized by the maximum amplitudes at each offset. (b) Confidence ellipses (95% confidence intervals of Chi-Square distribution) illustrating the k-space regions at 0 ppm with values greater than the median k-space value at 3.5 ppm. Ellipses were calculated using all 8 true experimental data and 50 randomly selected synthetic data respectively.
Fig. 4. Quantitative comparison of different datasets. (a) A manifold analysis of latent variables from various image datasets. The BraTS-CEST dataset has the shortest Riemannian distance from true experimental data. (b) Average reconstruction errors for CEST-VN and MoDL-CAT networks trained on BraTS-CEST and fastMRI-CEST datasets. The shaded regions represent the standard deviation σ of errors. nRMSE stands for normalized root mean squared error.
Fig. 5. Reconstruction results of 4-fold accelerated images using various methods. (a) Reconstructed APTw images and their corresponding errors versus fully sampled results from a glioma patient. (b) Boxplots illustrating nRMSE and SSIM pooled in all subjects for each reconstruction method. SSIM stands for structural similarity index.