Clinical Soma and Neurite Density Imaging ( SANDI ): Translational Microstructure Mapping on Clinical 3T MRI Scanners

ABSTRACT Purpose The Soma and Neurite Density Imaging (SANDI) model enables characterization of gray matter (GM) microstructure by estimating soma and neurite signal fractions, but its clinical applicability is limited by the need for multi‐shell acquisitions (at least five b ‐values up to 6000 s/mm 2 ), requiring high‐gradient MRI systems. We developed a clinically feasible SANDI model that reduces data requirements and model complexity while preserving sensitivity to cellular‐level microstructural features. Methods Clinical SANDI incorporates biophysical constraints via fixed intra‐neurite diffusivity and a tortuosity relation from effective medium theory to estimate extracellular diffusivity from intracellular volume fractions, reducing the number of free parameters and data requirements. The model was validated using Monte Carlo diffusion simulations in GM‐like microenvironments and evaluated in vivo on the ultra‐high‐gradient 3 T Connectome 2.0 scanner ( G max = 500 mT/m, five‐shell, ∼19 min) and a clinical 3 T system ( G max = 80 mT/m, two‐shell, ∼7 min). Additional experiments across multiple gradient strengths, diffusion times, and sites assessed model robustness. Results Diffusion simulations showed close agreement (Pearson r = 0.99) between simulated and theoretical extracellular diffusivity across varying intracellular volume fractions. With 500 mT/m gradients, clinical SANDI using two shells demonstrated strong correspondence with five‐shell standard SANDI ( r = 0.97, intraclass correlation coefficient = 0.94). Across reduced gradient strengths, clinical SANDI preserved cortical intra‐soma signal fraction values, whereas standard SANDI exhibited underestimation at gradient strengths below 80 mT/m. Conclusion Clinical SANDI enables reliable cortical GM microstructure estimation on widely available clinical 3T scanners within feasible scan times, facilitating broader translation of advanced diffusion MRI methods for studying aging, neurodegeneration, and neurological disorders.

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Journal
Magnetic Resonance in Medicine
Published
2026-08-27
DOI
https://doi.org/10.1002/mrm.70563
Primary Topic
Advanced Neuroimaging Techniques and Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Clinical Soma and Neurite Density Imaging ( SANDI ): Translational Microstructure Mapping on Clinical 3T MRI Scanners

HyungJoon Cho, Laleh Eskandarian, Hong‐Hsi Lee, Kwok‐Shing Chan et al.
Magnetic Resonance in Medicine
Advanced Neuroimaging Techniques and Applications
article

Clinical Soma and Neurite Density Imaging ( SANDI ): Translational Microstructure Mapping on Clinical 3T MRI Scanners

HyungJoon Cho, Laleh Eskandarian, Hong‐Hsi Lee, Kwok‐Shing Chan, Dongsuk Sung, Susie Y. Huang, Aneri Bhatt, Julianna Gerold, Eva A. Krijnen, DongKyu Lee, Yixin Ma, Sohyun Han, Hansol Lee
article en

Abstract

ABSTRACT Purpose The Soma and Neurite Density Imaging (SANDI) model enables characterization of gray matter (GM) microstructure by estimating soma and neurite signal fractions, but its clinical applicability is limited by the need for multi‐shell acquisitions (at least five b ‐values up to 6000 s/mm 2 ), requiring high‐gradient MRI systems. We developed a clinically feasible SANDI model that reduces data requirements and model complexity while preserving sensitivity to cellular‐level microstructural features. Methods Clinical SANDI incorporates biophysical constraints via fixed intra‐neurite diffusivity and a tortuosity relation from effective medium theory to estimate extracellular diffusivity from intracellular volume fractions, reducing the number of free parameters and data requirements. The model was validated using Monte Carlo diffusion simulations in GM‐like microenvironments and evaluated in vivo on the ultra‐high‐gradient 3 T Connectome 2.0 scanner ( G max = 500 mT/m, five‐shell, ∼19 min) and a clinical 3 T system ( G max = 80 mT/m, two‐shell, ∼7 min). Additional experiments across multiple gradient strengths, diffusion times, and sites assessed model robustness. Results Diffusion simulations showed close agreement (Pearson r = 0.99) between simulated and theoretical extracellular diffusivity across varying intracellular volume fractions. With 500 mT/m gradients, clinical SANDI using two shells demonstrated strong correspondence with five‐shell standard SANDI ( r = 0.97, intraclass correlation coefficient = 0.94). Across reduced gradient strengths, clinical SANDI preserved cortical intra‐soma signal fraction values, whereas standard SANDI exhibited underestimation at gradient strengths below 80 mT/m. Conclusion Clinical SANDI enables reliable cortical GM microstructure estimation on widely available clinical 3T scanners within feasible scan times, facilitating broader translation of advanced diffusion MRI methods for studying aging, neurodegeneration, and neurological disorders.

Magnetic Resonance in Medicine
Harvard University (US), Massachusetts General Hospital (US), Amsterdam Neuroscience (NL), Athinoula A. Martinos Center for Biomedical Imaging (US), Korea Basic Science Institute (KR), Korea Brain Research Institute (KR), Ulsan National Institute of Science and Technology (KR)
Korea Brain Research Institute, ZonMw, Nederlandse Organisatie voor Wetenschappelijk Onderzoek, National Research Council of Science and Technology, Ministry of Science and ICT, South Korea, National Institutes of Health, National Institute of Biomedical Imaging and Bioengineering
Openalex Percentile: Top 10%
Advanced Neuroimaging Techniques and Applications
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