Q-space trajectory imaging (QTI) provides promising markers of tissue microstructure, but clinical translation requires shorter acquisitions, faster analysis, and more robust parameter estimation at high spatial resolution. To address these barriers, we trained a voxel-wise multilayer perceptron (MLP) to infer QTI-derived scalar parameters directly from the diffusion signal. We established reference QTI parameters of the brain in 18 healthy subjects using constrained fitting on 50-min QTI scans. The MLP was trained to estimate those reference parameters from a five-minute subset of the diffusion data. We compared the MLP with the constrained fit applied to the same short-protocol input, computing normalized root mean squared error, peak signal-to-noise ratio, and structural similarity with respect to the reference. Here, the MLP consistently achieved better performance metrics, with normalized root mean squared errors up to two-fold lower. For one whole-brain dataset, MLP inference reduced computation time from more than an hour with constrained fitting to a few seconds. Robustness to lower SNR was tested in a separate 1.7 mm isotropic voxel size acquisition of the full protocol, in which the MLP retained lower errors and less visually apparent noise. Finally, we demonstrate qualitative feasibility in two glioma patients scanned with the short protocol. We conclude that a simple MLP can provide high-quality QTI parameter estimates from short tensor-valued diffusion acquisitions. This enables five-minute, high-resolution QTI and may encourage further clinical studies of markers such as microscopic fractional anisotropy.
Oliver Gödicke, Jin-Yang Yu, F. Laun et al.· Magnetic Resonance Imaging· 0 citations
Purpose: To complement 1.5-minute measurements of common tensor-valued diffusion MRI (dMRI) markers with rapid constrained fitting. Methods: Fast dMRI protocols for obtaining rotational invariants of the cumulant expansion (RICE) were paired with constrained weighted linear least squares (CWLLS) to stabilize the more fragile WLLS fit. A compact constraint set was formulated, including a novel mean-dependent upper bound on total diffusional variance. Evaluation used diffusion tensor distribution (DTD) simulations, healthy-volunteer data with a resolution-dependent SNR experiment, and a glioma patient dataset. A 5-minute q-space trajectory imaging (QTI) protocol served as a reference. Results: Across experiments, CWLLS reduced unphysical estimates and fit outliers in parameters such as microscopic FA and isotropic diffusivity variance. In simulations, it narrowed error distributions most clearly in the CSF-dominant case, while some metrics showed a bias-variance trade-off. In vivo, CWLLS removed negative variance estimates, truncated out-of-bounds tails, and reduced artifacts in fluid-contaminated voxels while preserving anatomical contrast. It also retained more stable maps than WLLS at higher resolution, although both estimators degraded in the lowest-SNR setting. Notably, the new mean-dependent variance bound was violated in 15.4% of voxels in the patient dataset, accounting for nearly half of the 32.7% that violated at least one constraint. Healthy-volunteer benchmarking showed that CWLLS completed in under 30 seconds. The constrained QTI fit required 72 minutes, making CWLLS 160 times faster. Conclusion: CWLLS for fast RICE yielded high-quality parameter maps at an online-ready computational cost. This may enhance the reliability of dMRI tissue characterization and strengthen the path toward clinical translation.
Jinyang Yu, Oliver Gödicke, F. Laun et al.· 0 citations
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