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Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA

PURPOSE: The mechanisms underlying the topography of motor deficits in spinal muscular atrophy (SMA) remain unknown. We investigated the profile of spinal cord atrophy (SCA) in SMN1-linked SMA, and its correlation with the topography of muscle weakness. MATERIALS AND METHODS: Eighteen SMN1-linked SM...

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Autores principales: El Mendili, Mohamed-Mounir, Lenglet, Timothée, Stojkovic, Tanya, Behin, Anthony, Guimarães-Costa, Raquel, Salachas, François, Meininger, Vincent, Bruneteau, Gaelle, Le Forestier, Nadine, Laforêt, Pascal, Lehéricy, Stéphane, Benali, Habib, Pradat, Pierre-François
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835076/
https://www.ncbi.nlm.nih.gov/pubmed/27089520
http://dx.doi.org/10.1371/journal.pone.0152439
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author El Mendili, Mohamed-Mounir
Lenglet, Timothée
Stojkovic, Tanya
Behin, Anthony
Guimarães-Costa, Raquel
Salachas, François
Meininger, Vincent
Bruneteau, Gaelle
Le Forestier, Nadine
Laforêt, Pascal
Lehéricy, Stéphane
Benali, Habib
Pradat, Pierre-François
author_facet El Mendili, Mohamed-Mounir
Lenglet, Timothée
Stojkovic, Tanya
Behin, Anthony
Guimarães-Costa, Raquel
Salachas, François
Meininger, Vincent
Bruneteau, Gaelle
Le Forestier, Nadine
Laforêt, Pascal
Lehéricy, Stéphane
Benali, Habib
Pradat, Pierre-François
author_sort El Mendili, Mohamed-Mounir
collection PubMed
description PURPOSE: The mechanisms underlying the topography of motor deficits in spinal muscular atrophy (SMA) remain unknown. We investigated the profile of spinal cord atrophy (SCA) in SMN1-linked SMA, and its correlation with the topography of muscle weakness. MATERIALS AND METHODS: Eighteen SMN1-linked SMA patients type III/V and 18 age/gender-matched healthy volunteers were included. Patients were scored on manual muscle testing and functional scales. Spinal cord was imaged using 3T MRI system. Radial distance (RD) and cord cross-sectional area (CSA) measurements in SMA patients were compared to those in controls and correlated with strength and disability scores. RESULTS: CSA measurements revealed a significant cord atrophy gradient mainly located between C3 and C6 vertebral levels with a SCA rate ranging from 5.4% to 23% in SMA patients compared to controls. RD was significantly lower in SMA patients compared to controls in the anterior-posterior direction with a maximum along C4 and C5 vertebral levels (p-values < 10(−5)). There were no correlations between atrophy measurements, strength and disability scores. CONCLUSIONS: Spinal cord atrophy in adult SMN1-linked SMA predominates in the segments innervating the proximal muscles. Additional factors such as neuromuscular junction or intrinsic skeletal muscle defects may play a role in more complex mechanisms underlying weakness in these patients.
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spelling pubmed-48350762016-04-29 Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA El Mendili, Mohamed-Mounir Lenglet, Timothée Stojkovic, Tanya Behin, Anthony Guimarães-Costa, Raquel Salachas, François Meininger, Vincent Bruneteau, Gaelle Le Forestier, Nadine Laforêt, Pascal Lehéricy, Stéphane Benali, Habib Pradat, Pierre-François PLoS One Research Article PURPOSE: The mechanisms underlying the topography of motor deficits in spinal muscular atrophy (SMA) remain unknown. We investigated the profile of spinal cord atrophy (SCA) in SMN1-linked SMA, and its correlation with the topography of muscle weakness. MATERIALS AND METHODS: Eighteen SMN1-linked SMA patients type III/V and 18 age/gender-matched healthy volunteers were included. Patients were scored on manual muscle testing and functional scales. Spinal cord was imaged using 3T MRI system. Radial distance (RD) and cord cross-sectional area (CSA) measurements in SMA patients were compared to those in controls and correlated with strength and disability scores. RESULTS: CSA measurements revealed a significant cord atrophy gradient mainly located between C3 and C6 vertebral levels with a SCA rate ranging from 5.4% to 23% in SMA patients compared to controls. RD was significantly lower in SMA patients compared to controls in the anterior-posterior direction with a maximum along C4 and C5 vertebral levels (p-values < 10(−5)). There were no correlations between atrophy measurements, strength and disability scores. CONCLUSIONS: Spinal cord atrophy in adult SMN1-linked SMA predominates in the segments innervating the proximal muscles. Additional factors such as neuromuscular junction or intrinsic skeletal muscle defects may play a role in more complex mechanisms underlying weakness in these patients. Public Library of Science 2016-04-18 /pmc/articles/PMC4835076/ /pubmed/27089520 http://dx.doi.org/10.1371/journal.pone.0152439 Text en © 2016 El Mendili et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
El Mendili, Mohamed-Mounir
Lenglet, Timothée
Stojkovic, Tanya
Behin, Anthony
Guimarães-Costa, Raquel
Salachas, François
Meininger, Vincent
Bruneteau, Gaelle
Le Forestier, Nadine
Laforêt, Pascal
Lehéricy, Stéphane
Benali, Habib
Pradat, Pierre-François
Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA
title Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA
title_full Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA
title_fullStr Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA
title_full_unstemmed Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA
title_short Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA
title_sort cervical spinal cord atrophy profile in adult smn1-linked sma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835076/
https://www.ncbi.nlm.nih.gov/pubmed/27089520
http://dx.doi.org/10.1371/journal.pone.0152439
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