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2D in-vivo L-COSY spectroscopy identifies neurometabolite alterations in treated multiple sclerosis
BACKGROUND: We have applied in vivo two-dimensional (2D) localized correlation spectroscopy (2D L-COSY), in treated relapsing relapsing-remitting multiple sclerosis (RRMS) to identify novel biomarkers in normal-appearing brain parenchyma. METHODS: 2D L-COSY magnetic resonance spectroscopy (MRS) spec...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801886/ https://www.ncbi.nlm.nih.gov/pubmed/31666809 http://dx.doi.org/10.1177/1756286419877081 |
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author | Quadrelli, Scott Ribbons, Karen Arm, Jameen Al-iedani, Oun Lechner-Scott, Jeannette Lea, Rodney Ramadan, Saadallah |
author_facet | Quadrelli, Scott Ribbons, Karen Arm, Jameen Al-iedani, Oun Lechner-Scott, Jeannette Lea, Rodney Ramadan, Saadallah |
author_sort | Quadrelli, Scott |
collection | PubMed |
description | BACKGROUND: We have applied in vivo two-dimensional (2D) localized correlation spectroscopy (2D L-COSY), in treated relapsing relapsing-remitting multiple sclerosis (RRMS) to identify novel biomarkers in normal-appearing brain parenchyma. METHODS: 2D L-COSY magnetic resonance spectroscopy (MRS) spectra were prospectively acquired from the posterior cingulate cortex (PCC) in 45 stable RRMS patients undergoing treatment with Fingolimod, and 40 age and sex-matched healthy control (HC) participants. Average metabolite ratios and clinical symptoms including, disability, cognition, fatigue, and mental health parameters were measured, and compared using parametric and nonparametric tests. Whole brain volume and MRS voxel morphometry were evaluated using SIENAX and the SPM LST toolbox. RESULTS: Despite the mean whole brain lesion volume being low in this RRMS group (6.8 ml) a significant reduction in PCC metabolite to tCr ratios were identified for multiple N-acetylaspartate (NAA) signatures, gamma-aminobutyric acid (GABA), glutamine and glutamate (Glx), threonine, and isoleucine/lipid. Of the clinical symptoms measured, visuospatial function, attention, and memory were correlated with NAA signatures, Glx, and isoleucine/lipid in the brain. CONCLUSIONS: 2D L-COSY has the potential to detect metabolic alterations in the normal-appearing MS brain. Despite examining only a localised region, we could detect metabolic variability associated with symptoms. |
format | Online Article Text |
id | pubmed-6801886 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-68018862019-10-30 2D in-vivo L-COSY spectroscopy identifies neurometabolite alterations in treated multiple sclerosis Quadrelli, Scott Ribbons, Karen Arm, Jameen Al-iedani, Oun Lechner-Scott, Jeannette Lea, Rodney Ramadan, Saadallah Ther Adv Neurol Disord Advances in Neuroimaging BACKGROUND: We have applied in vivo two-dimensional (2D) localized correlation spectroscopy (2D L-COSY), in treated relapsing relapsing-remitting multiple sclerosis (RRMS) to identify novel biomarkers in normal-appearing brain parenchyma. METHODS: 2D L-COSY magnetic resonance spectroscopy (MRS) spectra were prospectively acquired from the posterior cingulate cortex (PCC) in 45 stable RRMS patients undergoing treatment with Fingolimod, and 40 age and sex-matched healthy control (HC) participants. Average metabolite ratios and clinical symptoms including, disability, cognition, fatigue, and mental health parameters were measured, and compared using parametric and nonparametric tests. Whole brain volume and MRS voxel morphometry were evaluated using SIENAX and the SPM LST toolbox. RESULTS: Despite the mean whole brain lesion volume being low in this RRMS group (6.8 ml) a significant reduction in PCC metabolite to tCr ratios were identified for multiple N-acetylaspartate (NAA) signatures, gamma-aminobutyric acid (GABA), glutamine and glutamate (Glx), threonine, and isoleucine/lipid. Of the clinical symptoms measured, visuospatial function, attention, and memory were correlated with NAA signatures, Glx, and isoleucine/lipid in the brain. CONCLUSIONS: 2D L-COSY has the potential to detect metabolic alterations in the normal-appearing MS brain. Despite examining only a localised region, we could detect metabolic variability associated with symptoms. SAGE Publications 2019-10-19 /pmc/articles/PMC6801886/ /pubmed/31666809 http://dx.doi.org/10.1177/1756286419877081 Text en © The Author(s), 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Advances in Neuroimaging Quadrelli, Scott Ribbons, Karen Arm, Jameen Al-iedani, Oun Lechner-Scott, Jeannette Lea, Rodney Ramadan, Saadallah 2D in-vivo L-COSY spectroscopy identifies neurometabolite alterations in treated multiple sclerosis |
title | 2D in-vivo L-COSY spectroscopy identifies
neurometabolite alterations in treated multiple sclerosis |
title_full | 2D in-vivo L-COSY spectroscopy identifies
neurometabolite alterations in treated multiple sclerosis |
title_fullStr | 2D in-vivo L-COSY spectroscopy identifies
neurometabolite alterations in treated multiple sclerosis |
title_full_unstemmed | 2D in-vivo L-COSY spectroscopy identifies
neurometabolite alterations in treated multiple sclerosis |
title_short | 2D in-vivo L-COSY spectroscopy identifies
neurometabolite alterations in treated multiple sclerosis |
title_sort | 2d in-vivo l-cosy spectroscopy identifies
neurometabolite alterations in treated multiple sclerosis |
topic | Advances in Neuroimaging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801886/ https://www.ncbi.nlm.nih.gov/pubmed/31666809 http://dx.doi.org/10.1177/1756286419877081 |
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