Magnetic resonance neuroimaging is undergoing a major paradigm shift from traditional qualitative anatomical mapping toward integrated, quantitative measurement systems with biological interpretability. This review systematically synthesizes nine methodological pillars driving this transformation, encompassing advances ranging from hardware innovation to artificial intelligence algorithms. We first explore the pivotal role of deep learning in image reconstruction and acceleration, followed by detailed analyses of quantitative brain oxygen metabolism assessment, standardized spinal cord imaging frameworks, and the non-invasive monitoring of the glymphatic system using diffusion MRI. Furthermore, the review delves into tractometry, susceptibility-based myelin mapping, the clinical standardization of arterial spin labeling, and the application of radiomics in extracting high-dimensional phenotypes. Finally, the importance of open science and workflow coordination in enhancing research reproducibility is highlighted. Through the deep integration of hardware, sequences, and artificial intelligence, these technologies form a synergistic ecosystem that provides unprecedented precision tools and translational potential for both basic neuroscience research and clinical precision medicine. Across these domains, AI contributes not only to acceleration and reconstruction but also to segmentation, quality control, quantitative parameter extraction, and multiparametric pattern recognition that can support diagnostic interpretation. The quantitative emphasis of this review therefore lies in measurable outputs such as image-quality metrics, metabolic and perfusion parameters, tract-specific diffusion indices, susceptibility-based components, and radiomic features.
Xunyang Zhang, A. Hagiwara, Masaya Takahasi et al.· Japanese Journal of Radiolog...· 0 citations
PURPOSE
To develop and externally validate a non-invasive framework for quantifying brain amyloid-β (Aβ) deposition using magnetic resonance fingerprinting (MRF) and neural network-based decoding, with positron emission tomography (PET) as the reference standard.
METHODS
This prospective multi-site study included 44 participants from 2 sites who had undergone, or were scheduled to undergo, Aβ PET within 1 year. MRF was performed on a 3T MR system using a 2D fast imaging with steady-state precession sequence with B1 correction, covering the whole brain in 9.5 min. PET images were co-registered to the MRF space, and regional amyloid load was calculated using an automated template-based pipeline. An inverse mapping function was implemented to convert MRF signals into amyloid burden maps. Repeatability, agreement with PET-based centiloid values, and associations with cognitive scores were evaluated.
RESULTS
The generated amyloid maps were visually similar to PET images. Test-retest analysis showed high repeatability, with a coefficient of variation of 1.8 ± 1.3% and an intraclass correlation coefficient of 0.84. In the external test set, MRF-based measurements correlated significantly with PET centiloid scores (Spearman's ρ = 0.589, P = 0.015) and Montreal Cognitive Assessment scores (ρ = -0.543, P = 0.020).
CONCLUSION
The proposed framework enables non-invasive Aβ mapping using a clinically feasible MRI protocol and may support repeated assessment for monitoring during anti-amyloid treatment.
Shohei Fujita, Y. Fushimi, Y. Otsuka et al.· Magnetic Resonance in Medica...· 0 citations
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