Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Gray, Elizabeth, Larkin, James R., Claridge, Tim D. W., Talbot, Kevin, Sibson, Nicola R., Turner, Martin R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Informa Healthcare 2015
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
_version_ 1782411030449618944
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
work_keys_str_mv AT grayelizabeth thelongitudinalcerebrospinalfluidmetabolomicprofileofamyotrophiclateralsclerosis
AT larkinjamesr thelongitudinalcerebrospinalfluidmetabolomicprofileofamyotrophiclateralsclerosis
AT claridgetimdw thelongitudinalcerebrospinalfluidmetabolomicprofileofamyotrophiclateralsclerosis
AT talbotkevin thelongitudinalcerebrospinalfluidmetabolomicprofileofamyotrophiclateralsclerosis
AT sibsonnicolar thelongitudinalcerebrospinalfluidmetabolomicprofileofamyotrophiclateralsclerosis
AT turnermartinr thelongitudinalcerebrospinalfluidmetabolomicprofileofamyotrophiclateralsclerosis
AT grayelizabeth longitudinalcerebrospinalfluidmetabolomicprofileofamyotrophiclateralsclerosis
AT larkinjamesr longitudinalcerebrospinalfluidmetabolomicprofileofamyotrophiclateralsclerosis
AT claridgetimdw longitudinalcerebrospinalfluidmetabolomicprofileofamyotrophiclateralsclerosis
AT talbotkevin longitudinalcerebrospinalfluidmetabolomicprofileofamyotrophiclateralsclerosis
AT sibsonnicolar longitudinalcerebrospinalfluidmetabolomicprofileofamyotrophiclateralsclerosis
AT turnermartinr longitudinalcerebrospinalfluidmetabolomicprofileofamyotrophiclateralsclerosis