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Magnetic resonance imaging of the cervical spinal cord in spinal muscular atrophy

OBJECTIVE: In this study we investigated the potential value of magnetic resonance imaging (MRI) and diffusion tensor imaging (DTI) in characterizing changes in the cervical spinal cord and peripheral nerve roots in vivo in patients with spinal muscular atrophy (SMA). METHODS: We developed an MRI pr...

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Autores principales: Stam, Marloes, Haakma, Wieke, Kuster, Lidy, Froeling, Martijn, Philippens, Marielle E.P., Bos, Clemens, Leemans, Alexander, Otto, Louise A.M., van den Berg, Leonard H., Hendrikse, Jeroen, van der Pol, W. Ludo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812296/
https://www.ncbi.nlm.nih.gov/pubmed/31622841
http://dx.doi.org/10.1016/j.nicl.2019.102002
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author Stam, Marloes
Haakma, Wieke
Kuster, Lidy
Froeling, Martijn
Philippens, Marielle E.P.
Bos, Clemens
Leemans, Alexander
Otto, Louise A.M.
van den Berg, Leonard H.
Hendrikse, Jeroen
van der Pol, W. Ludo
author_facet Stam, Marloes
Haakma, Wieke
Kuster, Lidy
Froeling, Martijn
Philippens, Marielle E.P.
Bos, Clemens
Leemans, Alexander
Otto, Louise A.M.
van den Berg, Leonard H.
Hendrikse, Jeroen
van der Pol, W. Ludo
author_sort Stam, Marloes
collection PubMed
description OBJECTIVE: In this study we investigated the potential value of magnetic resonance imaging (MRI) and diffusion tensor imaging (DTI) in characterizing changes in the cervical spinal cord and peripheral nerve roots in vivo in patients with spinal muscular atrophy (SMA). METHODS: We developed an MRI protocol with 4 sequences to investigate the cervical spinal cord and nerve roots on a 3 Tesla MRI system. We used 2 anatomical MRI sequences to investigate cross-sectional area (CSA) at each spinal segment and the diameter of ventral and dorsal nerve roots, and two diffusion tensor imaging (DTI) techniques to estimate the fractional anisotropy (FA), mean (MD), axial (AD) and radial diffusivity (RD) in 10 SMA patients and 20 healthy controls. RESULTS: There were no significant differences in CSA (p > .1), although an 8.5% reduction of CSA in patients compared to healthy controls was apparent at segment C7. DTI data showed a higher AD in grey matter of patients compared to healthy controls (p = .033). Significantly lower MD, AD and RD values were found in rostral nerve roots (C3-C5) in patients (p < .045). CONCLUSIONS: We showed feasibility of an advanced 3 T MRI protocol that allowed differences to be determined between patients and healthy controls, confirming the potential of this technique to assess pathological mechanisms in SMA. After further development and confirmation of findings in a larger sample, these techniques may be used to study disease course of SMA in vivo and evaluate response to survival motor neuron (SMN) augmenting therapy.
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spelling pubmed-68122962019-10-30 Magnetic resonance imaging of the cervical spinal cord in spinal muscular atrophy Stam, Marloes Haakma, Wieke Kuster, Lidy Froeling, Martijn Philippens, Marielle E.P. Bos, Clemens Leemans, Alexander Otto, Louise A.M. van den Berg, Leonard H. Hendrikse, Jeroen van der Pol, W. Ludo Neuroimage Clin Regular Article OBJECTIVE: In this study we investigated the potential value of magnetic resonance imaging (MRI) and diffusion tensor imaging (DTI) in characterizing changes in the cervical spinal cord and peripheral nerve roots in vivo in patients with spinal muscular atrophy (SMA). METHODS: We developed an MRI protocol with 4 sequences to investigate the cervical spinal cord and nerve roots on a 3 Tesla MRI system. We used 2 anatomical MRI sequences to investigate cross-sectional area (CSA) at each spinal segment and the diameter of ventral and dorsal nerve roots, and two diffusion tensor imaging (DTI) techniques to estimate the fractional anisotropy (FA), mean (MD), axial (AD) and radial diffusivity (RD) in 10 SMA patients and 20 healthy controls. RESULTS: There were no significant differences in CSA (p > .1), although an 8.5% reduction of CSA in patients compared to healthy controls was apparent at segment C7. DTI data showed a higher AD in grey matter of patients compared to healthy controls (p = .033). Significantly lower MD, AD and RD values were found in rostral nerve roots (C3-C5) in patients (p < .045). CONCLUSIONS: We showed feasibility of an advanced 3 T MRI protocol that allowed differences to be determined between patients and healthy controls, confirming the potential of this technique to assess pathological mechanisms in SMA. After further development and confirmation of findings in a larger sample, these techniques may be used to study disease course of SMA in vivo and evaluate response to survival motor neuron (SMN) augmenting therapy. Elsevier 2019-09-03 /pmc/articles/PMC6812296/ /pubmed/31622841 http://dx.doi.org/10.1016/j.nicl.2019.102002 Text en © 2019 Published by Elsevier Inc. http://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
Stam, Marloes
Haakma, Wieke
Kuster, Lidy
Froeling, Martijn
Philippens, Marielle E.P.
Bos, Clemens
Leemans, Alexander
Otto, Louise A.M.
van den Berg, Leonard H.
Hendrikse, Jeroen
van der Pol, W. Ludo
Magnetic resonance imaging of the cervical spinal cord in spinal muscular atrophy
title Magnetic resonance imaging of the cervical spinal cord in spinal muscular atrophy
title_full Magnetic resonance imaging of the cervical spinal cord in spinal muscular atrophy
title_fullStr Magnetic resonance imaging of the cervical spinal cord in spinal muscular atrophy
title_full_unstemmed Magnetic resonance imaging of the cervical spinal cord in spinal muscular atrophy
title_short Magnetic resonance imaging of the cervical spinal cord in spinal muscular atrophy
title_sort magnetic resonance imaging of the cervical spinal cord in spinal muscular atrophy
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812296/
https://www.ncbi.nlm.nih.gov/pubmed/31622841
http://dx.doi.org/10.1016/j.nicl.2019.102002
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