Quantitative MRI findings indicate diffuse white matter damage in Susac Syndrome

Author:

Johnson PORCID,Chan JK1,Vavasour IM23ORCID,Abel SORCID,Lee LEORCID,Yong H1,Laule C2345,Li DKB12,Tam R26,Traboulsee A,Carruthers RL1ORCID,Kolind SH1235

Affiliation:

1. Department of Medicine (Neurology), University of British Columbia, Canada

2. Department of Radiology, University of British Columbia, Canada

3. International Collaboration on Repair Discoveries (ICORD)

4. Department of Pathology and Laboratory Medicine, University of British Columbia, Canada

5. Department of Physics and Astronomy, University of British Columbia, Canada

6. School of Biomedical Engineering, University of British Columbia, Canada

Abstract

Background Susac Syndrome (SuS) is an autoimmune endotheliopathy impacting the brain, retina and cochlea that can clinically mimic multiple sclerosis (MS). Objective To evaluate non-lesional white matter demyelination changes in SuS compared to MS and healthy controls (HC) using quantitative MRI. Methods 3T MRI including myelin water imaging and diffusion basis spectrum imaging were acquired for 7 SuS, 10 MS and 10 HC participants. Non-lesional white matter was analyzed in the corpus callosum (CC) and normal appearing white matter (NAWM). Groups were compared using ANCOVA with Tukey correction. Results SuS CC myelin water fraction (mean 0.092) was lower than MS(0.11, p = 0.01) and HC(0.11, p = 0.04). Another myelin marker, radial diffusivity, was increased in SuS CC(0.27μm2/ms) compared to HC(0.21μm2/ms, p = 0.008) and MS(0.23μm2/ms, p = 0.05). Fractional anisotropy was lower in SuS CC(0.82) than HC(0.86, p = 0.04). Fiber fraction (reflecting axons) did not differ from HC or MS. In NAWM, radial diffusivity and apparent diffusion coefficient were significantly increased in SuS compared to HC(p < 0.001 for both measures) and MS(p = 0.003, p < 0.001 respectively). Conclusions Our results provided evidence of myelin damage in SuS, particularly in the CC, and more extensive microstructural injury in NAWM, supporting the hypothesis that there are widespread microstructural changes in SuS syndrome including diffuse demyelination.

Funder

Multiple Sclerosis Society of Canada

Publisher

SAGE Publications

Subject

Cellular and Molecular Neuroscience,Neurology (clinical)

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