Metabolomic Changes in Patients Affected by Multiple Sclerosis and Treated with Fingolimod

Author:

Murgia Federica1ORCID,Lorefice Lorena2,Noto Antonio1,Spada Martina1,Frau Jessica2,Fenu Giuseppe2,Coghe Giancarlo2,Gagliano Antonella3ORCID,Atzori Luigi1ORCID,Cocco Eleonora4

Affiliation:

1. Department of Biomedical Sciences, Clinical Metabolomics Unit, University of Cagliari, 09124 Cagliari, Italy

2. Department of Medical Science and Public Health, University of Cagliari, 09124 Cagliari, Italy

3. Department of Health Science, “Magna Graecia” University of Catanzaro, 88100 Catanzaro, Italy

4. Multiple Sclerosis Center, Binaghi Hospital, ASSL Cagliari, 09126 Cagliari, Italy

Abstract

Current treatment for Multiple Sclerosis (MS) consists of a multidisciplinary approach including disease-modifying therapies. The response to treatment is heterogeneous, representing a crucial challenge in the classification of patients. Metabolomics is an innovative tool that can identifies biomarkers/predictors of treatment response. We aimed to evaluate plasma metabolic changes in a group of naïve Relapsing-Remitting MS patients starting Fingolimod treatment, to find specific metabolomic features that predict the therapeutic response as well as the possible side effects. The study included 42 Relapsing-Remitting MS blood samples, of which 30 were classified as responders after two years of FINGO treatment, whereas 12 patients were Not-Responders. For fifteen patients, samples were collected at four time points: before starting the therapy; at six months after the initiation; at twelve months after; and at twenty-four months after initiation. The serum was analysed through Nuclear Magnetic Resonance and multivariate and univariate statistical analysis. Considering the single comparison between each time point, it was possible to identify a set of metabolites changing their concentrations based on the drug intake. FINGO influences aminoacidic and energy metabolisms and reduces oxidative stress and the activity of the immune system, both typical features of MS.

Publisher

MDPI AG

Subject

Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

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