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Lipid profile of cerebrospinal fluid in multiple sclerosis patients: a potential tool for diagnosis
Multiple sclerosis (MS) is a complex multifactorial neuropathology. Although its etiology remains unclear, it has been demonstrated that the immune system attacks myelin, leading to demyelination and axonal damage. The involvement of lipids as one of the main components of myelin sheaths in MS and o...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6683197/ https://www.ncbi.nlm.nih.gov/pubmed/31383928 http://dx.doi.org/10.1038/s41598-019-47906-x |
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author | Nogueras, L. Gonzalo, H. Jové, M. Sol, J. Gil-Sanchez, A. Hervás, J. V. Valcheva, P. Gonzalez-Mingot, C. Solana, M. J. Peralta, S. Pamplona, R. Brieva, L. |
author_facet | Nogueras, L. Gonzalo, H. Jové, M. Sol, J. Gil-Sanchez, A. Hervás, J. V. Valcheva, P. Gonzalez-Mingot, C. Solana, M. J. Peralta, S. Pamplona, R. Brieva, L. |
author_sort | Nogueras, L. |
collection | PubMed |
description | Multiple sclerosis (MS) is a complex multifactorial neuropathology. Although its etiology remains unclear, it has been demonstrated that the immune system attacks myelin, leading to demyelination and axonal damage. The involvement of lipids as one of the main components of myelin sheaths in MS and other demyelinating diseases has been postulated. However, it is still a matter of debate whether specific alteration patterns exist over the disease course. Here, using a lipidomic approach, we demonstrated that, at the time of diagnosis, the cerebrospinal fluid of MS patients presented differences in 155 lipid species, 47 of which were identified. An initial hierarchical clusterization was used to classify MS patients based on the presence of 25 lipids. When a supervised method was applied in order to refine this classification, a lipidomic signature was obtained. This signature was composed of 15 molecules belonging to five different lipid families including fatty acids (FAs). An FA-targeted approach revealed differences in two members of this family: 18:3n3 and 20:0 (arachidic acid). These results reveal a CSF lipidomic signature in MS patients at the time of diagnosis that might be considered as a potential diagnostic tool. |
format | Online Article Text |
id | pubmed-6683197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66831972019-08-09 Lipid profile of cerebrospinal fluid in multiple sclerosis patients: a potential tool for diagnosis Nogueras, L. Gonzalo, H. Jové, M. Sol, J. Gil-Sanchez, A. Hervás, J. V. Valcheva, P. Gonzalez-Mingot, C. Solana, M. J. Peralta, S. Pamplona, R. Brieva, L. Sci Rep Article Multiple sclerosis (MS) is a complex multifactorial neuropathology. Although its etiology remains unclear, it has been demonstrated that the immune system attacks myelin, leading to demyelination and axonal damage. The involvement of lipids as one of the main components of myelin sheaths in MS and other demyelinating diseases has been postulated. However, it is still a matter of debate whether specific alteration patterns exist over the disease course. Here, using a lipidomic approach, we demonstrated that, at the time of diagnosis, the cerebrospinal fluid of MS patients presented differences in 155 lipid species, 47 of which were identified. An initial hierarchical clusterization was used to classify MS patients based on the presence of 25 lipids. When a supervised method was applied in order to refine this classification, a lipidomic signature was obtained. This signature was composed of 15 molecules belonging to five different lipid families including fatty acids (FAs). An FA-targeted approach revealed differences in two members of this family: 18:3n3 and 20:0 (arachidic acid). These results reveal a CSF lipidomic signature in MS patients at the time of diagnosis that might be considered as a potential diagnostic tool. Nature Publishing Group UK 2019-08-05 /pmc/articles/PMC6683197/ /pubmed/31383928 http://dx.doi.org/10.1038/s41598-019-47906-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Nogueras, L. Gonzalo, H. Jové, M. Sol, J. Gil-Sanchez, A. Hervás, J. V. Valcheva, P. Gonzalez-Mingot, C. Solana, M. J. Peralta, S. Pamplona, R. Brieva, L. Lipid profile of cerebrospinal fluid in multiple sclerosis patients: a potential tool for diagnosis |
title | Lipid profile of cerebrospinal fluid in multiple sclerosis patients: a potential tool for diagnosis |
title_full | Lipid profile of cerebrospinal fluid in multiple sclerosis patients: a potential tool for diagnosis |
title_fullStr | Lipid profile of cerebrospinal fluid in multiple sclerosis patients: a potential tool for diagnosis |
title_full_unstemmed | Lipid profile of cerebrospinal fluid in multiple sclerosis patients: a potential tool for diagnosis |
title_short | Lipid profile of cerebrospinal fluid in multiple sclerosis patients: a potential tool for diagnosis |
title_sort | lipid profile of cerebrospinal fluid in multiple sclerosis patients: a potential tool for diagnosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6683197/ https://www.ncbi.nlm.nih.gov/pubmed/31383928 http://dx.doi.org/10.1038/s41598-019-47906-x |
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