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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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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. |
format | Online Article Text |
id | pubmed-4835076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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