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Cord cross-sectional area at foramen magnum as a correlate of disability in amyotrophic lateral sclerosis

Spinal cord atrophy is one of the hallmarks of amyotrophic lateral sclerosis (ALS); however, it is not routinely assessed in routine clinical practice. In the present study, we evaluated whether spinal cord cross-sectional area measured at the foramen magnum level using a magnetic resonance imaging...

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Autores principales: Piaggio, Niccolò, Pardini, Matteo, Roccatagliata, Luca, Scialò, Carlo, Cabona, Corrado, Bonzano, Laura, Inglese, Matilde, Mancardi, Giovanni L., Caponnetto, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6015117/
https://www.ncbi.nlm.nih.gov/pubmed/29984352
http://dx.doi.org/10.1186/s41747-018-0045-6
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author Piaggio, Niccolò
Pardini, Matteo
Roccatagliata, Luca
Scialò, Carlo
Cabona, Corrado
Bonzano, Laura
Inglese, Matilde
Mancardi, Giovanni L.
Caponnetto, Claudia
author_facet Piaggio, Niccolò
Pardini, Matteo
Roccatagliata, Luca
Scialò, Carlo
Cabona, Corrado
Bonzano, Laura
Inglese, Matilde
Mancardi, Giovanni L.
Caponnetto, Claudia
author_sort Piaggio, Niccolò
collection PubMed
description Spinal cord atrophy is one of the hallmarks of amyotrophic lateral sclerosis (ALS); however, it is not routinely assessed in routine clinical practice. In the present study, we evaluated whether spinal cord cross-sectional area measured at the foramen magnum level using a magnetic resonance imaging head scan represents a clinically meaningful measure to be added to the whole-brain volume assessment. Using an active surface approach, we measured the cord area at the foramen magnum and brain parenchymal fraction on T1-weighted three-dimensional spoiled gradient recalled head scans in two groups of subjects: 23 patients with ALS (males/females, 13/10; mean ± standard deviation [SD] age 61.7 ± 10.3 years; median ALS Functional Rating Scale–Revised score 39, range 27–46) and 18 age- and sex-matched healthy volunteers (mean ± SD age 55.7 ± 10.2 years). Spinal cord area at the foramen magnum was significantly less in patients than in control subjects and was significantly correlated with disability as measured with the ALS Functional Rating Scale–Revised (ρ = 0.593, p <  0.005). This correlation remained significant after taking into account inter-individual differences in brain parenchymal fraction (ρ = 0.684, p <  0.001). Our data show that spinal cord area at the foramen magnum correlates with disability in ALS independently of whole-brain atrophy, thus indicating its potential as a disease biomarker.
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spelling pubmed-60151172018-07-04 Cord cross-sectional area at foramen magnum as a correlate of disability in amyotrophic lateral sclerosis Piaggio, Niccolò Pardini, Matteo Roccatagliata, Luca Scialò, Carlo Cabona, Corrado Bonzano, Laura Inglese, Matilde Mancardi, Giovanni L. Caponnetto, Claudia Eur Radiol Exp Technical Note Spinal cord atrophy is one of the hallmarks of amyotrophic lateral sclerosis (ALS); however, it is not routinely assessed in routine clinical practice. In the present study, we evaluated whether spinal cord cross-sectional area measured at the foramen magnum level using a magnetic resonance imaging head scan represents a clinically meaningful measure to be added to the whole-brain volume assessment. Using an active surface approach, we measured the cord area at the foramen magnum and brain parenchymal fraction on T1-weighted three-dimensional spoiled gradient recalled head scans in two groups of subjects: 23 patients with ALS (males/females, 13/10; mean ± standard deviation [SD] age 61.7 ± 10.3 years; median ALS Functional Rating Scale–Revised score 39, range 27–46) and 18 age- and sex-matched healthy volunteers (mean ± SD age 55.7 ± 10.2 years). Spinal cord area at the foramen magnum was significantly less in patients than in control subjects and was significantly correlated with disability as measured with the ALS Functional Rating Scale–Revised (ρ = 0.593, p <  0.005). This correlation remained significant after taking into account inter-individual differences in brain parenchymal fraction (ρ = 0.684, p <  0.001). Our data show that spinal cord area at the foramen magnum correlates with disability in ALS independently of whole-brain atrophy, thus indicating its potential as a disease biomarker. Springer International Publishing 2018-06-22 /pmc/articles/PMC6015117/ /pubmed/29984352 http://dx.doi.org/10.1186/s41747-018-0045-6 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Technical Note
Piaggio, Niccolò
Pardini, Matteo
Roccatagliata, Luca
Scialò, Carlo
Cabona, Corrado
Bonzano, Laura
Inglese, Matilde
Mancardi, Giovanni L.
Caponnetto, Claudia
Cord cross-sectional area at foramen magnum as a correlate of disability in amyotrophic lateral sclerosis
title Cord cross-sectional area at foramen magnum as a correlate of disability in amyotrophic lateral sclerosis
title_full Cord cross-sectional area at foramen magnum as a correlate of disability in amyotrophic lateral sclerosis
title_fullStr Cord cross-sectional area at foramen magnum as a correlate of disability in amyotrophic lateral sclerosis
title_full_unstemmed Cord cross-sectional area at foramen magnum as a correlate of disability in amyotrophic lateral sclerosis
title_short Cord cross-sectional area at foramen magnum as a correlate of disability in amyotrophic lateral sclerosis
title_sort cord cross-sectional area at foramen magnum as a correlate of disability in amyotrophic lateral sclerosis
topic Technical Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6015117/
https://www.ncbi.nlm.nih.gov/pubmed/29984352
http://dx.doi.org/10.1186/s41747-018-0045-6
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