Cargando…

Cervical cord myelin abnormality is associated with clinical disability in multiple sclerosis

BACKGROUND: Myelin water imaging (MWI) was recently optimized to provide quantitative in vivo measurement of spinal cord myelin, which is critically involved in multiple sclerosis (MS) disability. OBJECTIVE: To assess cervical cord myelin measurements in relapsing-remitting multiple sclerosis (RRMS)...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Lisa Eunyoung, Vavasour, Irene M, Dvorak, Adam, Liu, Hanwen, Abel, Shawna, Johnson, Poljanka, Ristow, Stephen, Au, Shelly, Laule, Cornelia, Tam, Roger, Li, David KB, Cross, Helen, Ackermans, Nathalie, Schabas, Alice J, Chan, Jillian, Sayao, Ana-Luiza, Devonshire, Virginia, Carruthers, Robert, Traboulsee, Anthony, Kolind, Shannon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597183/
https://www.ncbi.nlm.nih.gov/pubmed/33749378
http://dx.doi.org/10.1177/13524585211001780
Descripción
Sumario:BACKGROUND: Myelin water imaging (MWI) was recently optimized to provide quantitative in vivo measurement of spinal cord myelin, which is critically involved in multiple sclerosis (MS) disability. OBJECTIVE: To assess cervical cord myelin measurements in relapsing-remitting multiple sclerosis (RRMS) and progressive multiple sclerosis (ProgMS) participants and evaluate the correlation between myelin measures and clinical disability. METHODS: We used MWI data from 35 RRMS, 30 ProgMS, and 28 healthy control (HC) participants collected at cord level C2/C3 on a 3 T magnetic resonance imaging (MRI) scanner. Myelin heterogeneity index (MHI), a measurement of myelin variability, was calculated for whole cervical cord, global white matter, dorsal column, lateral and ventral funiculi. Correlations were assessed between MHI and Expanded Disability Status Scale (EDSS), 9-Hole Peg Test (9HPT), timed 25-foot walk, and disease duration. RESULTS: In various regions of the cervical cord, ProgMS MHI was higher compared to HC (between 9.5% and 31%, p ⩽ 0.04) and RRMS (between 13% and 26%, p ⩽ 0.02), and ProgMS MHI was associated with EDSS (r = 0.42–0.52) and 9HPT (r = 0.45–0.52). CONCLUSION: Myelin abnormalities within clinically eloquent areas are related to clinical disability. MWI metrics have a potential role for monitoring subclinical disease progression and adjudicating treatment efficacy for new therapies targeting ProgMS.