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Corpus callosum axon diameter relates to cognitive impairment in multiple sclerosis

Authors :
Qiuyun Fan
Sean M. Tobyne
Lawrence L. Wald
Thomas Witzel
Kevin R. Patel
Aapo Nummenmaa
John Daniel Bireley
Natalya Machado
Andrew W. Russo
Susie Y. Huang
Sarah F. Rapaport
Eric C. Klawiter
Janet C. Sherman
Ani Eloyan
Kristina Brewer
Source :
Annals of Clinical and Translational Neurology, Vol 6, Iss 5, Pp 882-892 (2019), Annals of Clinical and Translational Neurology
Publication Year :
2019
Publisher :
Wiley, 2019.

Abstract

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

Details

Language :
English
ISSN :
23289503
Volume :
6
Issue :
5
Database :
OpenAIRE
Journal :
Annals of Clinical and Translational Neurology
Accession number :
edsair.doi.dedup.....dc1a67aa16962f4c281fff742a6b4273