Bagnato, FrancescaFranco, GiuliaLi, HuaKaden, EnricoYe, FeiFan, RunChen, AmalieAlexander, Daniel C.Smith, Seth A.Dortch, RichardXu, Junzhong2020-07-162020-07-162019-09Bagnato, F., Franco, G., Li, H., Kaden, E., Ye, F., Fan, R., Chen, A., Alexander, D. C., Smith, S. A., Dortch, R., & Xu, J. (2019). Probing axons using multi-compartmental diffusion in multiple sclerosis. Annals of clinical and translational neurology, 6(9), 1595–1605. https://doi.org/10.1002/acn3.508362328-9503http://hdl.handle.net/1803/10213Objects The diffusion-based spherical mean technique (SMT) provides a novel model to relate multi-b-value diffusion magnetic resonance imaging (MRI) data to features of tissue microstructure. We propose the first clinical application of SMT to image the brain of patients with multiple sclerosis (MS) and investigate clinical feasibility and translation. Methods Eighteen MS patients and nine age- and sex-matched healthy controls (HCs) underwent a 3.0 Tesla scan inclusive of clinical sequences and SMT images (isotropic resolution of 2 mm). Axial diffusivity (AD), apparent axonal volume fraction (V-ax), and effective neural diffusivity (D-ax) parametric maps were fitted. Differences in AD, V-ax, and D-ax between anatomically matched regions reflecting different tissues types were estimated using generalized linear mixed models for binary outcomes. Results Differences were seen in all SMT-derived parameters between chronic black holes (cBHs) and T2-lesions (P <= 0.0016), in V-ax and AD between T2-lesions and normal appearing white matter (NAWM) (P < 0.0001), but not between the NAWM and normal WM in HCs. Inverse correlations were seen between V-ax and AD in cBHs (r = -0.750, P = 0.02); in T2-lesions D-ax values were associated with V-ax (r = 0.824, P < 0.0001) and AD (r = 0.570, P = 0.014). Interpretations SMT-derived metrics are sensitive to pathological changes and hold potential for clinical application in MS patients.en-USCopyright © 2019 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.BLACK-HOLESINFLAMMATIONQUANTIFICATIONDEMYELINATIONDISPERSIONINJURYProbing axons using multi-compartmental diffusion in multiple sclerosisArticle10.1002/acn3.50836