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Cerebrospinal fluid metabolomics: detection of neuroinflammation in human central nervous system disease
The high morbidity and mortality of neuroinflammatory diseases drives significant interest in understanding the underlying mechanisms involved in the innate and adaptive immune response of the central nervous system (CNS). Diagnostic biomarkers are important to define treatable neuroinflammation. Me...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343457/ https://www.ncbi.nlm.nih.gov/pubmed/34386234 http://dx.doi.org/10.1002/cti2.1318 |
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author | Yan, Jingya Kuzhiumparambil, Unnikrishnan Bandodkar, Sushil Dale, Russell C Fu, Shanlin |
author_facet | Yan, Jingya Kuzhiumparambil, Unnikrishnan Bandodkar, Sushil Dale, Russell C Fu, Shanlin |
author_sort | Yan, Jingya |
collection | PubMed |
description | The high morbidity and mortality of neuroinflammatory diseases drives significant interest in understanding the underlying mechanisms involved in the innate and adaptive immune response of the central nervous system (CNS). Diagnostic biomarkers are important to define treatable neuroinflammation. Metabolomics is a rapidly evolving research area offering novel insights into metabolic pathways, and elucidation of reliable metabolites as biomarkers for diseases. This review focuses on the emerging literature regarding the detection of neuroinflammation using cerebrospinal fluid (CSF) metabolomics in human cohort studies. Studies of classic neuroinflammatory disorders such as encephalitis, CNS infection and multiple sclerosis confirm the utility of CSF metabolomics. Additionally, studies in neurodegeneration and neuropsychiatry support the emerging potential of CSF metabolomics to detect neuroinflammation in common CNS diseases such as Alzheimer's disease and depression. We demonstrate metabolites in the tryptophan–kynurenine pathway, nitric oxide pathway, neopterin and major lipid species show moderately consistent ability to differentiate patients with neuroinflammation from controls. Integration of CSF metabolomics into clinical practice is warranted to improve recognition and treatment of neuroinflammation. |
format | Online Article Text |
id | pubmed-8343457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83434572021-08-11 Cerebrospinal fluid metabolomics: detection of neuroinflammation in human central nervous system disease Yan, Jingya Kuzhiumparambil, Unnikrishnan Bandodkar, Sushil Dale, Russell C Fu, Shanlin Clin Transl Immunology Reviews The high morbidity and mortality of neuroinflammatory diseases drives significant interest in understanding the underlying mechanisms involved in the innate and adaptive immune response of the central nervous system (CNS). Diagnostic biomarkers are important to define treatable neuroinflammation. Metabolomics is a rapidly evolving research area offering novel insights into metabolic pathways, and elucidation of reliable metabolites as biomarkers for diseases. This review focuses on the emerging literature regarding the detection of neuroinflammation using cerebrospinal fluid (CSF) metabolomics in human cohort studies. Studies of classic neuroinflammatory disorders such as encephalitis, CNS infection and multiple sclerosis confirm the utility of CSF metabolomics. Additionally, studies in neurodegeneration and neuropsychiatry support the emerging potential of CSF metabolomics to detect neuroinflammation in common CNS diseases such as Alzheimer's disease and depression. We demonstrate metabolites in the tryptophan–kynurenine pathway, nitric oxide pathway, neopterin and major lipid species show moderately consistent ability to differentiate patients with neuroinflammation from controls. Integration of CSF metabolomics into clinical practice is warranted to improve recognition and treatment of neuroinflammation. John Wiley and Sons Inc. 2021-08-06 /pmc/articles/PMC8343457/ /pubmed/34386234 http://dx.doi.org/10.1002/cti2.1318 Text en © 2021 The Authors. Clinical & Translational Immunology published by John Wiley & Sons Australia, Ltd on behalf of Australian and New Zealand Society for Immunology, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Reviews Yan, Jingya Kuzhiumparambil, Unnikrishnan Bandodkar, Sushil Dale, Russell C Fu, Shanlin Cerebrospinal fluid metabolomics: detection of neuroinflammation in human central nervous system disease |
title | Cerebrospinal fluid metabolomics: detection of neuroinflammation in human central nervous system disease |
title_full | Cerebrospinal fluid metabolomics: detection of neuroinflammation in human central nervous system disease |
title_fullStr | Cerebrospinal fluid metabolomics: detection of neuroinflammation in human central nervous system disease |
title_full_unstemmed | Cerebrospinal fluid metabolomics: detection of neuroinflammation in human central nervous system disease |
title_short | Cerebrospinal fluid metabolomics: detection of neuroinflammation in human central nervous system disease |
title_sort | cerebrospinal fluid metabolomics: detection of neuroinflammation in human central nervous system disease |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343457/ https://www.ncbi.nlm.nih.gov/pubmed/34386234 http://dx.doi.org/10.1002/cti2.1318 |
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