Metabolomics in multiple sclerosis disease course and progression.

Mult Scler

Department of Pharmacology, University of Oxford, Oxford, UK.

Published: April 2020

AI Article Synopsis

  • Multiple sclerosis (MS) is linked to noticeable changes in the metabolome, with various studies showing alterations in metabolic pathways in samples like brain tissue and urine.
  • Metabolomics can help differentiate MS patients from healthy individuals and other neurological disorders, potentially aiding in disease staging, progression monitoring, and therapy selection.
  • Future research aims to combine metabolomics with other omics techniques to deepen our understanding of MS and identify promising therapeutic targets.

Article Abstract

Multiple sclerosis (MS) is associated with changes in the metabolome. Numerous studies employing varying metabolomics platforms have examined a range of biological material ranging from brain tissue to urine and demonstrated consistently alterations in multiple metabolic pathways in MS. We review not only the studies that describe the ability of metabolomics to differentiate MS patients from healthy controls and other neurological disease but also discuss the potential of metabolomics-based methods to build predictive models that are able to stage disease, monitor progression, and select the most appropriate therapy. The increasing number of impressive claims for the capacity of metabolomics to distinguish between different types of demyelinating disease suggests that the provision of such tests may be close at hand. Besides the ability to provide potential diagnostic and prognostic biomarkers, metabolomics also provides us with unique insights into the pathophysiology of the disease and helps identify metabolic pathways that may be potential therapeutic targets. Future studies will integrate metabolomics data with other omics techniques to provide further insight into the source of these metabolic abnormalities and help with identification of the most promising targets for therapeutic intervention.

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Source
http://dx.doi.org/10.1177/1352458519876020DOI Listing

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