Cargando…
Simultaneous analysis of plasma and CSF by NMR and hierarchical models fusion
Because cerebrospinal fluid (CSF) is the biofluid which interacts most closely with the central nervous system, it holds promise as a reporter of neurological disease, for example multiple sclerosis (MScl). To characterize the metabolomics profile of neuroinflammatory aspects of this disease we stud...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3336062/ https://www.ncbi.nlm.nih.gov/pubmed/22395451 http://dx.doi.org/10.1007/s00216-012-5871-4 |
_version_ | 1782230880590233600 |
---|---|
author | Smolinska, Agnieszka Posma, Joram M. Blanchet, Lionel Ampt, Kirsten A. M. Attali, Amos Tuinstra, Tinka Luider, Theo Doskocz, Marek Michiels, Paul J. Girard, Frederic C. Buydens, Lutgarde M. C. Wijmenga, Sybren S. |
author_facet | Smolinska, Agnieszka Posma, Joram M. Blanchet, Lionel Ampt, Kirsten A. M. Attali, Amos Tuinstra, Tinka Luider, Theo Doskocz, Marek Michiels, Paul J. Girard, Frederic C. Buydens, Lutgarde M. C. Wijmenga, Sybren S. |
author_sort | Smolinska, Agnieszka |
collection | PubMed |
description | Because cerebrospinal fluid (CSF) is the biofluid which interacts most closely with the central nervous system, it holds promise as a reporter of neurological disease, for example multiple sclerosis (MScl). To characterize the metabolomics profile of neuroinflammatory aspects of this disease we studied an animal model of MScl—experimental autoimmune/allergic encephalomyelitis (EAE). Because CSF also exchanges metabolites with blood via the blood–brain barrier, malfunctions occurring in the CNS may be reflected in the biochemical composition of blood plasma. The combination of blood plasma and CSF provides more complete information about the disease. Both biofluids can be studied by use of NMR spectroscopy. It is then necessary to perform combined analysis of the two different datasets. Mid-level data fusion was therefore applied to blood plasma and CSF datasets. First, relevant information was extracted from each biofluid dataset by use of linear support vector machine recursive feature elimination. The selected variables from each dataset were concatenated for joint analysis by partial least squares discriminant analysis (PLS-DA). The combined metabolomics information from plasma and CSF enables more efficient and reliable discrimination of the onset of EAE. Second, we introduced hierarchical models fusion, in which previously developed PLS-DA models are hierarchically combined. We show that this approach enables neuroinflamed rats (even on the day of onset) to be distinguished from either healthy or peripherally inflamed rats. Moreover, progression of EAE can be investigated because the model separates the onset and peak of the disease. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00216-012-5871-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3336062 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-33360622012-05-14 Simultaneous analysis of plasma and CSF by NMR and hierarchical models fusion Smolinska, Agnieszka Posma, Joram M. Blanchet, Lionel Ampt, Kirsten A. M. Attali, Amos Tuinstra, Tinka Luider, Theo Doskocz, Marek Michiels, Paul J. Girard, Frederic C. Buydens, Lutgarde M. C. Wijmenga, Sybren S. Anal Bioanal Chem Original Paper Because cerebrospinal fluid (CSF) is the biofluid which interacts most closely with the central nervous system, it holds promise as a reporter of neurological disease, for example multiple sclerosis (MScl). To characterize the metabolomics profile of neuroinflammatory aspects of this disease we studied an animal model of MScl—experimental autoimmune/allergic encephalomyelitis (EAE). Because CSF also exchanges metabolites with blood via the blood–brain barrier, malfunctions occurring in the CNS may be reflected in the biochemical composition of blood plasma. The combination of blood plasma and CSF provides more complete information about the disease. Both biofluids can be studied by use of NMR spectroscopy. It is then necessary to perform combined analysis of the two different datasets. Mid-level data fusion was therefore applied to blood plasma and CSF datasets. First, relevant information was extracted from each biofluid dataset by use of linear support vector machine recursive feature elimination. The selected variables from each dataset were concatenated for joint analysis by partial least squares discriminant analysis (PLS-DA). The combined metabolomics information from plasma and CSF enables more efficient and reliable discrimination of the onset of EAE. Second, we introduced hierarchical models fusion, in which previously developed PLS-DA models are hierarchically combined. We show that this approach enables neuroinflamed rats (even on the day of onset) to be distinguished from either healthy or peripherally inflamed rats. Moreover, progression of EAE can be investigated because the model separates the onset and peak of the disease. [Figure: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00216-012-5871-4) contains supplementary material, which is available to authorized users. Springer-Verlag 2012-03-07 2012 /pmc/articles/PMC3336062/ /pubmed/22395451 http://dx.doi.org/10.1007/s00216-012-5871-4 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Paper Smolinska, Agnieszka Posma, Joram M. Blanchet, Lionel Ampt, Kirsten A. M. Attali, Amos Tuinstra, Tinka Luider, Theo Doskocz, Marek Michiels, Paul J. Girard, Frederic C. Buydens, Lutgarde M. C. Wijmenga, Sybren S. Simultaneous analysis of plasma and CSF by NMR and hierarchical models fusion |
title | Simultaneous analysis of plasma and CSF by NMR and hierarchical models fusion |
title_full | Simultaneous analysis of plasma and CSF by NMR and hierarchical models fusion |
title_fullStr | Simultaneous analysis of plasma and CSF by NMR and hierarchical models fusion |
title_full_unstemmed | Simultaneous analysis of plasma and CSF by NMR and hierarchical models fusion |
title_short | Simultaneous analysis of plasma and CSF by NMR and hierarchical models fusion |
title_sort | simultaneous analysis of plasma and csf by nmr and hierarchical models fusion |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3336062/ https://www.ncbi.nlm.nih.gov/pubmed/22395451 http://dx.doi.org/10.1007/s00216-012-5871-4 |
work_keys_str_mv | AT smolinskaagnieszka simultaneousanalysisofplasmaandcsfbynmrandhierarchicalmodelsfusion AT posmajoramm simultaneousanalysisofplasmaandcsfbynmrandhierarchicalmodelsfusion AT blanchetlionel simultaneousanalysisofplasmaandcsfbynmrandhierarchicalmodelsfusion AT amptkirstenam simultaneousanalysisofplasmaandcsfbynmrandhierarchicalmodelsfusion AT attaliamos simultaneousanalysisofplasmaandcsfbynmrandhierarchicalmodelsfusion AT tuinstratinka simultaneousanalysisofplasmaandcsfbynmrandhierarchicalmodelsfusion AT luidertheo simultaneousanalysisofplasmaandcsfbynmrandhierarchicalmodelsfusion AT doskoczmarek simultaneousanalysisofplasmaandcsfbynmrandhierarchicalmodelsfusion AT michielspaulj simultaneousanalysisofplasmaandcsfbynmrandhierarchicalmodelsfusion AT girardfredericc simultaneousanalysisofplasmaandcsfbynmrandhierarchicalmodelsfusion AT buydenslutgardemc simultaneousanalysisofplasmaandcsfbynmrandhierarchicalmodelsfusion AT wijmengasybrens simultaneousanalysisofplasmaandcsfbynmrandhierarchicalmodelsfusion |