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Corpus callosum axon diameter relates to cognitive impairment in multiple sclerosis

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journal contribution
posted on 2019-05-30, 21:22 authored by Susie Y. Huang, Qiuyun Fan, Natalya Machado, Ani Eloyan, John Bireley, Andrew Russo, Sean Tobyne, Kevin Patel, Kristina Brewer, Sarah Rapaport, Aapo Nummenmaa, Thomas Witzel, Janet Sherman, Lawrence L. Wald, Eric Klawiter
Objective: To evaluate alterations in apparent axon diameter and axon density obtained by high-gradient diffusion MRI in the corpus callosum of MS patients and the relationship of these advanced diffusion MRI metrics to neurologic disability and cognitive impairment in MS. Methods: Thirty people with MS (23 relapsing-remitting MS [RRMS], 7 progressive MS [PMS]) and 23 healthy controls were scanned on a human 3-tesla (3T) MRI scanner equipped with 300 mT/m maximum gradient strength using a comprehensive multishell diffusion MRI protocol. Data were fitted to a three-compartment geometric model of white matter to estimate apparent axon diameter and axon density in the midline corpus callosum. Neurologic disability and cognitive function were measured using the Expanded Disability Status Scale (EDSS), Multiple Sclerosis Functional Composite (MSFC), and Minimal Assessment of Cognitive Function in MS battery. Results: Apparent axon diameter was significantly larger and axon density reduced in the normal-appearing corpus callosum (NACC) of MS patients compared to healthy controls, with similar trends seen in PMS compared to RRMS. Larger apparent axon diameter in the NACC of MS patients correlated with greater disability as measured by the EDSS (r = 0.555, P = 0.007) and poorer performance on the Symbol Digits Modalities Test (r = -0.593, P = 0.008) and Brief Visuospatial Memory Test-Revised (r = 0.632, P < 0.01), tests of interhemispheric processing speed and new learning and memory, respectively. Interpretation: Apparent axon diameter in the corpus callosum obtained from high-gradient diffusion MRI is a potential imaging biomarker that may be used to understand the development and progression of cognitive impairment in MS.


Grant ID

K23NS096056, K23NS078044, R00EB015445, P41EB015896

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