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HDL-cholesterol elevation associated with fingolimod and dimethyl fumarate therapies in multiple sclerosis
BACKGROUND: Patients with Multiple Sclerosis (PwMS) display altered lipoproteins levels and function, which seem to affect disease risk and progress. Whether disease-modifying therapies affect the lipoprotein profile in PwMS has scarcely been studied. OBJECTIVE: The study aims to assess whether fing...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794658/ https://www.ncbi.nlm.nih.gov/pubmed/31662882 http://dx.doi.org/10.1177/2055217319882720 |
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author | Blumenfeld Kan, S Staun-Ram, E Golan, D Miller, A |
author_facet | Blumenfeld Kan, S Staun-Ram, E Golan, D Miller, A |
author_sort | Blumenfeld Kan, S |
collection | PubMed |
description | BACKGROUND: Patients with Multiple Sclerosis (PwMS) display altered lipoproteins levels and function, which seem to affect disease risk and progress. Whether disease-modifying therapies affect the lipoprotein profile in PwMS has scarcely been studied. OBJECTIVE: The study aims to assess whether fingolimod and dimethyl fumarate (DMF) affect lipoproteins in PwMS. METHODS: We compared retrospectively the blood lipoprotein levels of 29 fingolimod-treated and 41 DMF-treated patients before and after 3 and 12 months of therapy. Patients treated with cholesterol-reducing medications were not included. Data on weight change and disease activity during 1-year follow-up were obtained. RESULTS: HDL level, HDL/LDL ratio and HDL/total cholesterol ratio were increased in both treatment groups after 3 months’ therapy and sustained, with no change in LDL or triglycerides. While at baseline only 26% of patients met the recommended minimum of HDL 60 mg/dl, after 3 months’ therapy, 43% of fingolimod-treated and 47% of DMF-treated patients reached the recommended level. The majority of patients had no weight reduction. CONCLUSIONS: Fingolimod and DMF therapies are associated with a specific increase in HDL in PwMS. Further studies are required to validate these findings and their potential implication as biomarker of reduced inflammatory state and/or reduced risk of neurodegeneration or cardiovascular comorbidity. |
format | Online Article Text |
id | pubmed-6794658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-67946582019-10-29 HDL-cholesterol elevation associated with fingolimod and dimethyl fumarate therapies in multiple sclerosis Blumenfeld Kan, S Staun-Ram, E Golan, D Miller, A Mult Scler J Exp Transl Clin Original Research Paper BACKGROUND: Patients with Multiple Sclerosis (PwMS) display altered lipoproteins levels and function, which seem to affect disease risk and progress. Whether disease-modifying therapies affect the lipoprotein profile in PwMS has scarcely been studied. OBJECTIVE: The study aims to assess whether fingolimod and dimethyl fumarate (DMF) affect lipoproteins in PwMS. METHODS: We compared retrospectively the blood lipoprotein levels of 29 fingolimod-treated and 41 DMF-treated patients before and after 3 and 12 months of therapy. Patients treated with cholesterol-reducing medications were not included. Data on weight change and disease activity during 1-year follow-up were obtained. RESULTS: HDL level, HDL/LDL ratio and HDL/total cholesterol ratio were increased in both treatment groups after 3 months’ therapy and sustained, with no change in LDL or triglycerides. While at baseline only 26% of patients met the recommended minimum of HDL 60 mg/dl, after 3 months’ therapy, 43% of fingolimod-treated and 47% of DMF-treated patients reached the recommended level. The majority of patients had no weight reduction. CONCLUSIONS: Fingolimod and DMF therapies are associated with a specific increase in HDL in PwMS. Further studies are required to validate these findings and their potential implication as biomarker of reduced inflammatory state and/or reduced risk of neurodegeneration or cardiovascular comorbidity. SAGE Publications 2019-10-14 /pmc/articles/PMC6794658/ /pubmed/31662882 http://dx.doi.org/10.1177/2055217319882720 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Paper Blumenfeld Kan, S Staun-Ram, E Golan, D Miller, A HDL-cholesterol elevation associated with fingolimod and dimethyl fumarate therapies in multiple sclerosis |
title | HDL-cholesterol elevation associated with fingolimod and dimethyl
fumarate therapies in multiple sclerosis |
title_full | HDL-cholesterol elevation associated with fingolimod and dimethyl
fumarate therapies in multiple sclerosis |
title_fullStr | HDL-cholesterol elevation associated with fingolimod and dimethyl
fumarate therapies in multiple sclerosis |
title_full_unstemmed | HDL-cholesterol elevation associated with fingolimod and dimethyl
fumarate therapies in multiple sclerosis |
title_short | HDL-cholesterol elevation associated with fingolimod and dimethyl
fumarate therapies in multiple sclerosis |
title_sort | hdl-cholesterol elevation associated with fingolimod and dimethyl
fumarate therapies in multiple sclerosis |
topic | Original Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6794658/ https://www.ncbi.nlm.nih.gov/pubmed/31662882 http://dx.doi.org/10.1177/2055217319882720 |
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