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Relapsing-remitting multiple sclerosis patients display an altered lipoprotein profile with dysfunctional HDL

Lipoproteins modulate innate and adaptive immune responses. In the chronic inflammatory disease multiple sclerosis (MS), reports on lipoprotein level alterations are inconsistent and it is unclear whether lipoprotein function is affected. Using nuclear magnetic resonance (NMR) spectroscopy, we analy...

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Autores principales: Jorissen, Winde, Wouters, Elien, Bogie, Jeroen F., Vanmierlo, Tim, Noben, Jean-Paul, Sviridov, Denis, Hellings, Niels, Somers, Veerle, Valcke, Roland, Vanwijmeersch, Bart, Stinissen, Piet, Mulder, Monique T., Remaley, Alan T., Hendriks, Jerome J. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5322497/
https://www.ncbi.nlm.nih.gov/pubmed/28230201
http://dx.doi.org/10.1038/srep43410
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author Jorissen, Winde
Wouters, Elien
Bogie, Jeroen F.
Vanmierlo, Tim
Noben, Jean-Paul
Sviridov, Denis
Hellings, Niels
Somers, Veerle
Valcke, Roland
Vanwijmeersch, Bart
Stinissen, Piet
Mulder, Monique T.
Remaley, Alan T.
Hendriks, Jerome J. A.
author_facet Jorissen, Winde
Wouters, Elien
Bogie, Jeroen F.
Vanmierlo, Tim
Noben, Jean-Paul
Sviridov, Denis
Hellings, Niels
Somers, Veerle
Valcke, Roland
Vanwijmeersch, Bart
Stinissen, Piet
Mulder, Monique T.
Remaley, Alan T.
Hendriks, Jerome J. A.
author_sort Jorissen, Winde
collection PubMed
description Lipoproteins modulate innate and adaptive immune responses. In the chronic inflammatory disease multiple sclerosis (MS), reports on lipoprotein level alterations are inconsistent and it is unclear whether lipoprotein function is affected. Using nuclear magnetic resonance (NMR) spectroscopy, we analysed the lipoprotein profile of relapsing-remitting (RR) MS patients, progressive MS patients and healthy controls (HC). We observed smaller LDL in RRMS patients compared to healthy controls and to progressive MS patients. Furthermore, low-BMI (BMI ≤ 23 kg/m(2)) RRMS patients show increased levels of small HDL (sHDL), accompanied by larger, triglyceride (TG)-rich VLDL, and a higher lipoprotein insulin resistance (LP-IR) index. These alterations coincide with a reduced serum capacity to accept cholesterol via ATP-binding cassette (ABC) transporter G1, an impaired ability of HDL(3) to suppress inflammatory activity of human monocytes, and modifications of HDL(3)’s main protein component ApoA-I. In summary, lipoprotein levels and function are altered in RRMS patients, especially in low-BMI patients, which may contribute to disease progression in these patients.
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spelling pubmed-53224972017-03-01 Relapsing-remitting multiple sclerosis patients display an altered lipoprotein profile with dysfunctional HDL Jorissen, Winde Wouters, Elien Bogie, Jeroen F. Vanmierlo, Tim Noben, Jean-Paul Sviridov, Denis Hellings, Niels Somers, Veerle Valcke, Roland Vanwijmeersch, Bart Stinissen, Piet Mulder, Monique T. Remaley, Alan T. Hendriks, Jerome J. A. Sci Rep Article Lipoproteins modulate innate and adaptive immune responses. In the chronic inflammatory disease multiple sclerosis (MS), reports on lipoprotein level alterations are inconsistent and it is unclear whether lipoprotein function is affected. Using nuclear magnetic resonance (NMR) spectroscopy, we analysed the lipoprotein profile of relapsing-remitting (RR) MS patients, progressive MS patients and healthy controls (HC). We observed smaller LDL in RRMS patients compared to healthy controls and to progressive MS patients. Furthermore, low-BMI (BMI ≤ 23 kg/m(2)) RRMS patients show increased levels of small HDL (sHDL), accompanied by larger, triglyceride (TG)-rich VLDL, and a higher lipoprotein insulin resistance (LP-IR) index. These alterations coincide with a reduced serum capacity to accept cholesterol via ATP-binding cassette (ABC) transporter G1, an impaired ability of HDL(3) to suppress inflammatory activity of human monocytes, and modifications of HDL(3)’s main protein component ApoA-I. In summary, lipoprotein levels and function are altered in RRMS patients, especially in low-BMI patients, which may contribute to disease progression in these patients. Nature Publishing Group 2017-02-23 /pmc/articles/PMC5322497/ /pubmed/28230201 http://dx.doi.org/10.1038/srep43410 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Jorissen, Winde
Wouters, Elien
Bogie, Jeroen F.
Vanmierlo, Tim
Noben, Jean-Paul
Sviridov, Denis
Hellings, Niels
Somers, Veerle
Valcke, Roland
Vanwijmeersch, Bart
Stinissen, Piet
Mulder, Monique T.
Remaley, Alan T.
Hendriks, Jerome J. A.
Relapsing-remitting multiple sclerosis patients display an altered lipoprotein profile with dysfunctional HDL
title Relapsing-remitting multiple sclerosis patients display an altered lipoprotein profile with dysfunctional HDL
title_full Relapsing-remitting multiple sclerosis patients display an altered lipoprotein profile with dysfunctional HDL
title_fullStr Relapsing-remitting multiple sclerosis patients display an altered lipoprotein profile with dysfunctional HDL
title_full_unstemmed Relapsing-remitting multiple sclerosis patients display an altered lipoprotein profile with dysfunctional HDL
title_short Relapsing-remitting multiple sclerosis patients display an altered lipoprotein profile with dysfunctional HDL
title_sort relapsing-remitting multiple sclerosis patients display an altered lipoprotein profile with dysfunctional hdl
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5322497/
https://www.ncbi.nlm.nih.gov/pubmed/28230201
http://dx.doi.org/10.1038/srep43410
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