Cargando…

Patterns of white and gray structural abnormality associated with paediatric demyelinating disorders

The impact of multiple sclerosis (MS) and myelin oligodendrocyte glycoprotein (MOG) - associated disorders (MOGAD) on brain structure in youth remains poorly understood. Reductions in cortical mantle thickness on structural MRI and abnormal diffusion-based white matter metrics (e.g., diffusion tenso...

Descripción completa

Detalles Bibliográficos
Autores principales: Bells, Sonya, Longoni, Giulia, Berenbaum, Tara, de Medeiros, Cynthia B., Narayanan, Sridar, Banwell, Brenda L., Arnold, Douglas L., Mabbott, Donald J., Ann Yeh, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8980471/
https://www.ncbi.nlm.nih.gov/pubmed/35381508
http://dx.doi.org/10.1016/j.nicl.2022.103001
_version_ 1784681401201721344
author Bells, Sonya
Longoni, Giulia
Berenbaum, Tara
de Medeiros, Cynthia B.
Narayanan, Sridar
Banwell, Brenda L.
Arnold, Douglas L.
Mabbott, Donald J.
Ann Yeh, E.
author_facet Bells, Sonya
Longoni, Giulia
Berenbaum, Tara
de Medeiros, Cynthia B.
Narayanan, Sridar
Banwell, Brenda L.
Arnold, Douglas L.
Mabbott, Donald J.
Ann Yeh, E.
author_sort Bells, Sonya
collection PubMed
description The impact of multiple sclerosis (MS) and myelin oligodendrocyte glycoprotein (MOG) - associated disorders (MOGAD) on brain structure in youth remains poorly understood. Reductions in cortical mantle thickness on structural MRI and abnormal diffusion-based white matter metrics (e.g., diffusion tensor parameters) have been well documented in MS but not in MOGAD. Characterizing structural abnormalities found in children with these disorders can help clarify the differences and similarities in their impact on neuroanatomy. Importantly, while MS and MOGAD affect the entire CNS, the visual pathway is of particular interest in both groups, as most patients have evidence for clinical or subclinical involvement of the anterior visual pathway. Thus, the visual pathway is of key interest in analyses of structural abnormalities in these disorders and may distinguish MOGAD from MS patients. In this study we collected MRI data on 18 MS patients, 14 MOGAD patients and 26 age- and sex-matched typically developing children (TDC). Full-brain group differences in fixel diffusion measures (fibre-bundle populations) and cortical thickness measures were tested using age and sex as covariates. Visual pathway analysis was performed by extracting mean diffusion measures within lesion free optic radiations, cortical thickness within the visual cortex, and retinal nerve fibre layer (RNFL) and ganglion cell layer thickness measures from optical coherence tomography (OCT). Fixel based analysis (FBA) revealed MS patients have widespread abnormal white matter within the corticospinal tract, inferior longitudinal fasciculus, and optic radiations, while within MOGAD patients, non-lesional impact on white matter was found primarily in the right optic radiation. Cortical thickness measures were reduced predominately in the temporal and parietal lobes in MS patients and in frontal, cingulate and visual cortices in MOGAD patients. Additionally, our findings of associations between reduced RNFLT and axonal density in MOGAD and TORT in MS patients in the optic radiations imply widespread axonal and myelin damage in the visual pathway, respectively. Overall, our approach of combining FBA, cortical thickness and OCT measures has helped evaluate similarities and differences in brain structure in MS and MOGAD patients in comparison to TDC.
format Online
Article
Text
id pubmed-8980471
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-89804712022-04-06 Patterns of white and gray structural abnormality associated with paediatric demyelinating disorders Bells, Sonya Longoni, Giulia Berenbaum, Tara de Medeiros, Cynthia B. Narayanan, Sridar Banwell, Brenda L. Arnold, Douglas L. Mabbott, Donald J. Ann Yeh, E. Neuroimage Clin Regular Article The impact of multiple sclerosis (MS) and myelin oligodendrocyte glycoprotein (MOG) - associated disorders (MOGAD) on brain structure in youth remains poorly understood. Reductions in cortical mantle thickness on structural MRI and abnormal diffusion-based white matter metrics (e.g., diffusion tensor parameters) have been well documented in MS but not in MOGAD. Characterizing structural abnormalities found in children with these disorders can help clarify the differences and similarities in their impact on neuroanatomy. Importantly, while MS and MOGAD affect the entire CNS, the visual pathway is of particular interest in both groups, as most patients have evidence for clinical or subclinical involvement of the anterior visual pathway. Thus, the visual pathway is of key interest in analyses of structural abnormalities in these disorders and may distinguish MOGAD from MS patients. In this study we collected MRI data on 18 MS patients, 14 MOGAD patients and 26 age- and sex-matched typically developing children (TDC). Full-brain group differences in fixel diffusion measures (fibre-bundle populations) and cortical thickness measures were tested using age and sex as covariates. Visual pathway analysis was performed by extracting mean diffusion measures within lesion free optic radiations, cortical thickness within the visual cortex, and retinal nerve fibre layer (RNFL) and ganglion cell layer thickness measures from optical coherence tomography (OCT). Fixel based analysis (FBA) revealed MS patients have widespread abnormal white matter within the corticospinal tract, inferior longitudinal fasciculus, and optic radiations, while within MOGAD patients, non-lesional impact on white matter was found primarily in the right optic radiation. Cortical thickness measures were reduced predominately in the temporal and parietal lobes in MS patients and in frontal, cingulate and visual cortices in MOGAD patients. Additionally, our findings of associations between reduced RNFLT and axonal density in MOGAD and TORT in MS patients in the optic radiations imply widespread axonal and myelin damage in the visual pathway, respectively. Overall, our approach of combining FBA, cortical thickness and OCT measures has helped evaluate similarities and differences in brain structure in MS and MOGAD patients in comparison to TDC. Elsevier 2022-03-31 /pmc/articles/PMC8980471/ /pubmed/35381508 http://dx.doi.org/10.1016/j.nicl.2022.103001 Text en © 2022 Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Bells, Sonya
Longoni, Giulia
Berenbaum, Tara
de Medeiros, Cynthia B.
Narayanan, Sridar
Banwell, Brenda L.
Arnold, Douglas L.
Mabbott, Donald J.
Ann Yeh, E.
Patterns of white and gray structural abnormality associated with paediatric demyelinating disorders
title Patterns of white and gray structural abnormality associated with paediatric demyelinating disorders
title_full Patterns of white and gray structural abnormality associated with paediatric demyelinating disorders
title_fullStr Patterns of white and gray structural abnormality associated with paediatric demyelinating disorders
title_full_unstemmed Patterns of white and gray structural abnormality associated with paediatric demyelinating disorders
title_short Patterns of white and gray structural abnormality associated with paediatric demyelinating disorders
title_sort patterns of white and gray structural abnormality associated with paediatric demyelinating disorders
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8980471/
https://www.ncbi.nlm.nih.gov/pubmed/35381508
http://dx.doi.org/10.1016/j.nicl.2022.103001
work_keys_str_mv AT bellssonya patternsofwhiteandgraystructuralabnormalityassociatedwithpaediatricdemyelinatingdisorders
AT longonigiulia patternsofwhiteandgraystructuralabnormalityassociatedwithpaediatricdemyelinatingdisorders
AT berenbaumtara patternsofwhiteandgraystructuralabnormalityassociatedwithpaediatricdemyelinatingdisorders
AT demedeiroscynthiab patternsofwhiteandgraystructuralabnormalityassociatedwithpaediatricdemyelinatingdisorders
AT narayanansridar patternsofwhiteandgraystructuralabnormalityassociatedwithpaediatricdemyelinatingdisorders
AT banwellbrendal patternsofwhiteandgraystructuralabnormalityassociatedwithpaediatricdemyelinatingdisorders
AT arnolddouglasl patternsofwhiteandgraystructuralabnormalityassociatedwithpaediatricdemyelinatingdisorders
AT mabbottdonaldj patternsofwhiteandgraystructuralabnormalityassociatedwithpaediatricdemyelinatingdisorders
AT annyehe patternsofwhiteandgraystructuralabnormalityassociatedwithpaediatricdemyelinatingdisorders