ArticleFrontiers in neurology2025
Diagnostic performance of a multi-shell DTI protocol and its subsets with B-matrix spatial distribution correction in differentiating early multiple sclerosis patients from healthy controls.
Article in Frontiers in neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Preserved neurovascular coupling in early multiple sclerosis is associated with reduced white matter lesion burden.Therapeutic advances in neurological disorders · 2026Article
- Tensor-derived diffusion MRI metrics and NODDI in multiple sclerosis classification.NeuroImage. Clinical · 2026Article
- A review of multiple sclerosis: From pathophysiology to latest therapeutic advances.AIMS neuroscience · 2025Review
- T1- and diffusion tensor-based fractal dimension of white and grey matter in multiple sclerosis.Frontiers in neurology · 2025Article
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Authors and funding
3 authors.
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Abstract
Introduction: This study investigates whether a multi-shell diffusion tensor imaging (DTI) protocol and its subsets can reliably distinguish healthy controls (HC) from patients with multiple sclerosis (MS) presenting with low Expanded Disability Status Scale (EDSS) scores and mild MRI findings. Methods: To enhance accuracy, spatial systematic errors in diffusion measurements were corrected using the B-matrix Spatial Distribution method (BSD-DTI). We examined the discriminative potential of fractional anisotropy (FA) and mean diffusivity (MD) across three broad brain regions: whole brain (WB), white matter (WM), and gray matter (GM), using both the full protocol and its subsets. Additionally, we employed a more detailed classification strategy based on segmentation into 95 regions of interest (ROIs), analyzing FA, MD, axial diffusivity (AD), and radial diffusivity (RD) under a stringent statistical criterion. Results: While the protocol and each subset showed a comparable ability to differentiate between HC and MS groups, substantial variability in metric values across protocols highlights the limited utility of directly comparing DTI metrics between acquisition schemes. Discussion: The results emphasize the importance of accounting for spatial systematic errors when selecting optimal protocols for clinical and research applications.
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