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Dimethyl fumarate treatment induces lipid metabolism alterations that are linked to immunological changes

OBJECTIVE: Identify metabolic changes produced by dimethyl fumarate (DMF) treatment and link them to immunological effects. METHODS: We enrolled 18 MS patients and obtained blood prior to DMF and 6 months postinitiation. We also enrolled 18 healthy controls for comparison. We performed global metabo...

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Autores principales: Bhargava, Pavan, Fitzgerald, Kathryn C., Venkata, Swarajya L. V., Smith, Matthew D., Kornberg, Michael D., Mowry, Ellen M., Haughey, Norman J., Calabresi, Peter A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331509/
https://www.ncbi.nlm.nih.gov/pubmed/30656182
http://dx.doi.org/10.1002/acn3.676
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author Bhargava, Pavan
Fitzgerald, Kathryn C.
Venkata, Swarajya L. V.
Smith, Matthew D.
Kornberg, Michael D.
Mowry, Ellen M.
Haughey, Norman J.
Calabresi, Peter A.
author_facet Bhargava, Pavan
Fitzgerald, Kathryn C.
Venkata, Swarajya L. V.
Smith, Matthew D.
Kornberg, Michael D.
Mowry, Ellen M.
Haughey, Norman J.
Calabresi, Peter A.
author_sort Bhargava, Pavan
collection PubMed
description OBJECTIVE: Identify metabolic changes produced by dimethyl fumarate (DMF) treatment and link them to immunological effects. METHODS: We enrolled 18 MS patients and obtained blood prior to DMF and 6 months postinitiation. We also enrolled 18 healthy controls for comparison. We performed global metabolomics on plasma and used weighted correlation network analysis (WGCNA) to identify modules of correlated metabolites. We identified modules that changed with treatment, followed by targeted metabolomics to corroborate changes identified in global analyses. We correlated changes in metabolite modules and individual metabolites with changes in immunological parameters. RESULTS: We identified alterations in lipid metabolism after DMF treatment – increases in two modules (phospholipids, lysophospholipids and plasmalogens) and reduction in one module (saturated and poly‐unsaturated fatty acids) eigen‐metabolite values (all P < 0.05). Change in the fatty acid module was greater in participants who developed lymphopenia and was strongly associated with both reduction in absolute lymphocyte counts (r = 0.65; P = 0.005) and change in CD8+ T cell subsets. We also noted significant correlation of change in lymphocyte counts with multiple fatty acid levels (measured by targeted or untargeted methods). INTERPRETATION: This study demonstrates that DMF treatment alters lipid metabolism and that changes in fatty acid levels are related to DMF‐induced immunological changes.
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spelling pubmed-63315092019-01-17 Dimethyl fumarate treatment induces lipid metabolism alterations that are linked to immunological changes Bhargava, Pavan Fitzgerald, Kathryn C. Venkata, Swarajya L. V. Smith, Matthew D. Kornberg, Michael D. Mowry, Ellen M. Haughey, Norman J. Calabresi, Peter A. Ann Clin Transl Neurol Research Articles OBJECTIVE: Identify metabolic changes produced by dimethyl fumarate (DMF) treatment and link them to immunological effects. METHODS: We enrolled 18 MS patients and obtained blood prior to DMF and 6 months postinitiation. We also enrolled 18 healthy controls for comparison. We performed global metabolomics on plasma and used weighted correlation network analysis (WGCNA) to identify modules of correlated metabolites. We identified modules that changed with treatment, followed by targeted metabolomics to corroborate changes identified in global analyses. We correlated changes in metabolite modules and individual metabolites with changes in immunological parameters. RESULTS: We identified alterations in lipid metabolism after DMF treatment – increases in two modules (phospholipids, lysophospholipids and plasmalogens) and reduction in one module (saturated and poly‐unsaturated fatty acids) eigen‐metabolite values (all P < 0.05). Change in the fatty acid module was greater in participants who developed lymphopenia and was strongly associated with both reduction in absolute lymphocyte counts (r = 0.65; P = 0.005) and change in CD8+ T cell subsets. We also noted significant correlation of change in lymphocyte counts with multiple fatty acid levels (measured by targeted or untargeted methods). INTERPRETATION: This study demonstrates that DMF treatment alters lipid metabolism and that changes in fatty acid levels are related to DMF‐induced immunological changes. John Wiley and Sons Inc. 2018-10-30 /pmc/articles/PMC6331509/ /pubmed/30656182 http://dx.doi.org/10.1002/acn3.676 Text en © 2018 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals, Inc on behalf of American Neurological Association. This is an open access article under the terms of the http://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 Research Articles
Bhargava, Pavan
Fitzgerald, Kathryn C.
Venkata, Swarajya L. V.
Smith, Matthew D.
Kornberg, Michael D.
Mowry, Ellen M.
Haughey, Norman J.
Calabresi, Peter A.
Dimethyl fumarate treatment induces lipid metabolism alterations that are linked to immunological changes
title Dimethyl fumarate treatment induces lipid metabolism alterations that are linked to immunological changes
title_full Dimethyl fumarate treatment induces lipid metabolism alterations that are linked to immunological changes
title_fullStr Dimethyl fumarate treatment induces lipid metabolism alterations that are linked to immunological changes
title_full_unstemmed Dimethyl fumarate treatment induces lipid metabolism alterations that are linked to immunological changes
title_short Dimethyl fumarate treatment induces lipid metabolism alterations that are linked to immunological changes
title_sort dimethyl fumarate treatment induces lipid metabolism alterations that are linked to immunological changes
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331509/
https://www.ncbi.nlm.nih.gov/pubmed/30656182
http://dx.doi.org/10.1002/acn3.676
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