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April 09, 2019; 92 (15) Editorial

Evolution of regional brain atrophy in children with multiple sclerosis

Gray matters

E. Ann Yeh, View ORCID ProfileArman Eshaghi
First published March 13, 2019, DOI: https://doi.org/10.1212/WNL.0000000000007254
E. Ann Yeh
From the Division of Neurology (E.A.Y.), Department of Pediatrics, Division of Neuroscience and Mental Health, SickKids Research Institute, The Hospital for Sick Children, and University of Toronto, Canada; and Queen Square Multiple Sclerosis Centre, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences (A.E.), and Centre for Medical Image Computing, Department of Computer Science (A.E.), University College London, UK.
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Arman Eshaghi
From the Division of Neurology (E.A.Y.), Department of Pediatrics, Division of Neuroscience and Mental Health, SickKids Research Institute, The Hospital for Sick Children, and University of Toronto, Canada; and Queen Square Multiple Sclerosis Centre, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences (A.E.), and Centre for Medical Image Computing, Department of Computer Science (A.E.), University College London, UK.
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Evolution of regional brain atrophy in children with multiple sclerosis
Gray matters
E. Ann Yeh, Arman Eshaghi
Neurology Apr 2019, 92 (15) 694-695; DOI: 10.1212/WNL.0000000000007254

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While multiple sclerosis (MS) has classically been considered to be a white matter disease, it is now clear that gray matter changes are seen at onset. Importantly, regional gray matter atrophy correlates strongly with motor outcomes in adult patients.1 Individuals with pediatric-onset MS have greater disease burden, as evidenced by higher relapse rate2 and increased lesion volume and atrophy on MRI3 than those with adult-onset MS. Furthermore, cognitive decline may be seen as early as 2 years after diagnosis in this population.4 Importantly, studies of structural correlates of disease progression in pediatric-onset MS must take the dynamic and maturational changes known to occur in the pediatric brain into account, including age- and sex-specific growth in some areas and regression and pruning in others.5 To this end, previous studies focused on white matter tracts and head size in pediatric-onset MS, and showed alterations in growth trajectories in patients with pediatric-onset MS in comparison with healthy youth.6 Others have demonstrated the extent of gray matter injury in the pediatric MS population, but have largely focused on specific deep gray matter structures.7 Much less is known about the dynamic pattern of growth and regression of various gray matter regions, and their relationship to outcomes in the pediatric patients with MS.

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  • Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

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  • © 2019 American Academy of Neurology
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