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Proton magnetic resonance spectroscopy of human cervical spondylosis at 3T

STUDY DESIGN: A single center magnetic resonance imaging and spectroscopic study involving twenty-one patients with advanced cervical spondylosis and eleven healthy controls. OBJECTIVE: We assessed the utility of MR spectroscopy to quantify biochemical changes within the spinal cord and serve as a p...

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Autores principales: Salamon, Noriko, Ellingson, Benjamin M., Nagarajan, Rajakumar, Gebara, Nathalie, Thomas, Albert, Holly, Langston T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3703492/
https://www.ncbi.nlm.nih.gov/pubmed/23588574
http://dx.doi.org/10.1038/sc.2013.31
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author Salamon, Noriko
Ellingson, Benjamin M.
Nagarajan, Rajakumar
Gebara, Nathalie
Thomas, Albert
Holly, Langston T.
author_facet Salamon, Noriko
Ellingson, Benjamin M.
Nagarajan, Rajakumar
Gebara, Nathalie
Thomas, Albert
Holly, Langston T.
author_sort Salamon, Noriko
collection PubMed
description STUDY DESIGN: A single center magnetic resonance imaging and spectroscopic study involving twenty-one patients with advanced cervical spondylosis and eleven healthy controls. OBJECTIVE: We assessed the utility of MR spectroscopy to quantify biochemical changes within the spinal cord and serve as a potential biomarker in patients with cervical spondylosis with or without T2 hyperintensity within the cord. SETTING: Los Angeles, California, USA METHODS: Twenty-one patients with cervical spondylosis and eleven healthy controls were evaluated. Single voxel MR spectroscopy was performed in the cervical cord. Morphometry of the spinal canal space was measured. NAA, choline, myo-inositol, glutamine-glutamate complex and lactate metabolite concentration ratios with respect to total creatine were quantified using an LC model algorithm and compared between healthy controls and spondylosis patients. Correlation of MRS metabolites with mJOA score was also performed. RESULTS: The spinal canal space was significantly different between patients and controls (ANOVA, P<0.0001). Total choline-to creatine-ratio was significantly elevated in patients with spondylosis and T2-hyperintensity compared with healthy controls (ANOVA, P<0.01). A significantly higher choline-to-NAA ratio was observed in spondylosis patients compared with healthy controls (ANOVA, P<0.01). Slightly elevated glutamine-glutamate complex and myo-inositol was encountered in patients with stenosis without T2 hyperintensity. A linear correlation between Cho-NAA ratio and mJOA was also observed (P<0.01). CONCLUSION: MRS appears sensitive to biochemical changes occurring in advanced cervical spondylosis patients. The choline/NAA ratio was significantly correlated with the mJOA score, providing a potentially clinical useful radiographical biomarker for the management of advanced cervical spondylosis patients.
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spelling pubmed-37034922014-01-01 Proton magnetic resonance spectroscopy of human cervical spondylosis at 3T Salamon, Noriko Ellingson, Benjamin M. Nagarajan, Rajakumar Gebara, Nathalie Thomas, Albert Holly, Langston T. Spinal Cord Article STUDY DESIGN: A single center magnetic resonance imaging and spectroscopic study involving twenty-one patients with advanced cervical spondylosis and eleven healthy controls. OBJECTIVE: We assessed the utility of MR spectroscopy to quantify biochemical changes within the spinal cord and serve as a potential biomarker in patients with cervical spondylosis with or without T2 hyperintensity within the cord. SETTING: Los Angeles, California, USA METHODS: Twenty-one patients with cervical spondylosis and eleven healthy controls were evaluated. Single voxel MR spectroscopy was performed in the cervical cord. Morphometry of the spinal canal space was measured. NAA, choline, myo-inositol, glutamine-glutamate complex and lactate metabolite concentration ratios with respect to total creatine were quantified using an LC model algorithm and compared between healthy controls and spondylosis patients. Correlation of MRS metabolites with mJOA score was also performed. RESULTS: The spinal canal space was significantly different between patients and controls (ANOVA, P<0.0001). Total choline-to creatine-ratio was significantly elevated in patients with spondylosis and T2-hyperintensity compared with healthy controls (ANOVA, P<0.01). A significantly higher choline-to-NAA ratio was observed in spondylosis patients compared with healthy controls (ANOVA, P<0.01). Slightly elevated glutamine-glutamate complex and myo-inositol was encountered in patients with stenosis without T2 hyperintensity. A linear correlation between Cho-NAA ratio and mJOA was also observed (P<0.01). CONCLUSION: MRS appears sensitive to biochemical changes occurring in advanced cervical spondylosis patients. The choline/NAA ratio was significantly correlated with the mJOA score, providing a potentially clinical useful radiographical biomarker for the management of advanced cervical spondylosis patients. 2013-04-16 2013-07 /pmc/articles/PMC3703492/ /pubmed/23588574 http://dx.doi.org/10.1038/sc.2013.31 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Salamon, Noriko
Ellingson, Benjamin M.
Nagarajan, Rajakumar
Gebara, Nathalie
Thomas, Albert
Holly, Langston T.
Proton magnetic resonance spectroscopy of human cervical spondylosis at 3T
title Proton magnetic resonance spectroscopy of human cervical spondylosis at 3T
title_full Proton magnetic resonance spectroscopy of human cervical spondylosis at 3T
title_fullStr Proton magnetic resonance spectroscopy of human cervical spondylosis at 3T
title_full_unstemmed Proton magnetic resonance spectroscopy of human cervical spondylosis at 3T
title_short Proton magnetic resonance spectroscopy of human cervical spondylosis at 3T
title_sort proton magnetic resonance spectroscopy of human cervical spondylosis at 3t
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3703492/
https://www.ncbi.nlm.nih.gov/pubmed/23588574
http://dx.doi.org/10.1038/sc.2013.31
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