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Probing axons using multi-compartmental diffusion in multiple sclerosis

dc.contributor.authorBagnato, Francesca
dc.contributor.authorFranco, Giulia
dc.contributor.authorLi, Hua
dc.contributor.authorKaden, Enrico
dc.contributor.authorYe, Fei
dc.contributor.authorFan, Run
dc.contributor.authorChen, Amalie
dc.contributor.authorAlexander, Daniel C.
dc.contributor.authorSmith, Seth A.
dc.contributor.authorDortch, Richard
dc.contributor.authorXu, Junzhong
dc.date.accessioned2020-07-16T21:50:54Z
dc.date.available2020-07-16T21:50:54Z
dc.date.issued2019-09
dc.identifier.citationBagnato, 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/acn3.50836en_US
dc.identifier.issn2328-9503
dc.identifier.urihttp://hdl.handle.net/1803/10213
dc.description.abstractObjects 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_US
dc.description.sponsorshipSources of support include: extramural program of the National Institutes of Health (NIH) (NIBIB K01 EB009120, R01 EB000461, and K25 EB013659), the Clinical and Translational Science Awards (UL1TR000445-06 from National Center for Advancing Translational Sciences/NIH), the European Union Horizon 2020 (EU H2020 634541-2), the EPSRC (Engineering and Physical Sciences Research Council), United Kingdom (UK) (UK EPSRC EP/M020533/1, UK EPSRC EP/N018702/1), the National MS Society (MS Clinical Mentorship Program, NMSS PP-180129686 and NMSS RG-1501-02840).en_US
dc.language.isoen_USen_US
dc.publisherAnnals of Clinical and Translational Neurologyen_US
dc.rightsCopyright © 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.
dc.source.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764633/
dc.subjectBLACK-HOLESen_US
dc.subjectINFLAMMATIONen_US
dc.subjectQUANTIFICATIONen_US
dc.subjectDEMYELINATIONen_US
dc.subjectDISPERSIONen_US
dc.subjectINJURYen_US
dc.titleProbing axons using multi-compartmental diffusion in multiple sclerosisen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/acn3.50836


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