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The longitudinal cerebrospinal fluid metabolomic profile of amyotrophic lateral sclerosis
Neurochemical biomarkers are urgently sought in ALS. Metabolomic analysis of cerebrospinal fluid (CSF) using proton nuclear magnetic resonance ((1)H-NMR) spectroscopy is a highly sensitive method capable of revealing nervous system cellular pathology. The (1)H-NMR CSF metabolomic signature of ALS wa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Informa Healthcare
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4720042/ https://www.ncbi.nlm.nih.gov/pubmed/26121274 http://dx.doi.org/10.3109/21678421.2015.1053490 |
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author | Gray, Elizabeth Larkin, James R. Claridge, Tim D. W. Talbot, Kevin Sibson, Nicola R. Turner, Martin R. |
author_facet | Gray, Elizabeth Larkin, James R. Claridge, Tim D. W. Talbot, Kevin Sibson, Nicola R. Turner, Martin R. |
author_sort | Gray, Elizabeth |
collection | PubMed |
description | Neurochemical biomarkers are urgently sought in ALS. Metabolomic analysis of cerebrospinal fluid (CSF) using proton nuclear magnetic resonance ((1)H-NMR) spectroscopy is a highly sensitive method capable of revealing nervous system cellular pathology. The (1)H-NMR CSF metabolomic signature of ALS was sought in a longitudinal cohort. Six-monthly serial collection was performed in ALS patients across a range of clinical sub-types (n = 41) for up to two years, and in healthy controls at a single time-point (n = 14). A multivariate statistical approach, partial least squares discriminant analysis, was used to determine differences between the NMR spectra from patients and controls. Significantly predictive models were found using those patients with at least one year's interval between recruitment and the second sample. Glucose, lactate, citric acid and, unexpectedly, ethanol were the discriminating metabolites elevated in ALS. It is concluded that (1)H-NMR captured the CSF metabolomic signature associated with derangements in cellular energy utilization connected with ALS, and was most prominent in comparisons using patients with longer disease duration. The specific metabolites identified support the concept of a hypercatabolic state, possibly involving mitochondrial dysfunction specifically. Endogenous ethanol in the CSF may be an unrecognized novel marker of neuronal tissue injury in ALS. |
format | Online Article Text |
id | pubmed-4720042 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Informa Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-47200422016-02-05 The longitudinal cerebrospinal fluid metabolomic profile of amyotrophic lateral sclerosis Gray, Elizabeth Larkin, James R. Claridge, Tim D. W. Talbot, Kevin Sibson, Nicola R. Turner, Martin R. Amyotroph Lateral Scler Frontotemporal Degener Original Article Neurochemical biomarkers are urgently sought in ALS. Metabolomic analysis of cerebrospinal fluid (CSF) using proton nuclear magnetic resonance ((1)H-NMR) spectroscopy is a highly sensitive method capable of revealing nervous system cellular pathology. The (1)H-NMR CSF metabolomic signature of ALS was sought in a longitudinal cohort. Six-monthly serial collection was performed in ALS patients across a range of clinical sub-types (n = 41) for up to two years, and in healthy controls at a single time-point (n = 14). A multivariate statistical approach, partial least squares discriminant analysis, was used to determine differences between the NMR spectra from patients and controls. Significantly predictive models were found using those patients with at least one year's interval between recruitment and the second sample. Glucose, lactate, citric acid and, unexpectedly, ethanol were the discriminating metabolites elevated in ALS. It is concluded that (1)H-NMR captured the CSF metabolomic signature associated with derangements in cellular energy utilization connected with ALS, and was most prominent in comparisons using patients with longer disease duration. The specific metabolites identified support the concept of a hypercatabolic state, possibly involving mitochondrial dysfunction specifically. Endogenous ethanol in the CSF may be an unrecognized novel marker of neuronal tissue injury in ALS. Informa Healthcare 2015-11-27 2015-06-29 /pmc/articles/PMC4720042/ /pubmed/26121274 http://dx.doi.org/10.3109/21678421.2015.1053490 Text en © 2015 Informa Healthcare 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 work is properly cited. |
spellingShingle | Original Article Gray, Elizabeth Larkin, James R. Claridge, Tim D. W. Talbot, Kevin Sibson, Nicola R. Turner, Martin R. The longitudinal cerebrospinal fluid metabolomic profile of amyotrophic lateral sclerosis |
title | The longitudinal cerebrospinal fluid metabolomic profile of amyotrophic lateral sclerosis |
title_full | The longitudinal cerebrospinal fluid metabolomic profile of amyotrophic lateral sclerosis |
title_fullStr | The longitudinal cerebrospinal fluid metabolomic profile of amyotrophic lateral sclerosis |
title_full_unstemmed | The longitudinal cerebrospinal fluid metabolomic profile of amyotrophic lateral sclerosis |
title_short | The longitudinal cerebrospinal fluid metabolomic profile of amyotrophic lateral sclerosis |
title_sort | longitudinal cerebrospinal fluid metabolomic profile of amyotrophic lateral sclerosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4720042/ https://www.ncbi.nlm.nih.gov/pubmed/26121274 http://dx.doi.org/10.3109/21678421.2015.1053490 |
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