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Lipoprotein hydrophobic core lipids are partially extruded to surface in smaller HDL: “Herniated” HDL, a common feature in diabetes

Recent studies have shown that pharmacological increases in HDL cholesterol concentrations do not necessarily translate into clinical benefits for patients, raising concerns about its predictive value for cardiovascular events. Here we hypothesize that the size-modulated lipid distribution within HD...

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Autores principales: Amigó, Núria, Mallol, Roger, Heras, Mercedes, Martínez-Hervás, Sergio, Blanco-Vaca, Francisco, Escolà-Gil, Joan Carles, Plana, Núria, Yanes, Óscar, Masana, Lluís, Correig, Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726105/
https://www.ncbi.nlm.nih.gov/pubmed/26778677
http://dx.doi.org/10.1038/srep19249
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author Amigó, Núria
Mallol, Roger
Heras, Mercedes
Martínez-Hervás, Sergio
Blanco-Vaca, Francisco
Escolà-Gil, Joan Carles
Plana, Núria
Yanes, Óscar
Masana, Lluís
Correig, Xavier
author_facet Amigó, Núria
Mallol, Roger
Heras, Mercedes
Martínez-Hervás, Sergio
Blanco-Vaca, Francisco
Escolà-Gil, Joan Carles
Plana, Núria
Yanes, Óscar
Masana, Lluís
Correig, Xavier
author_sort Amigó, Núria
collection PubMed
description Recent studies have shown that pharmacological increases in HDL cholesterol concentrations do not necessarily translate into clinical benefits for patients, raising concerns about its predictive value for cardiovascular events. Here we hypothesize that the size-modulated lipid distribution within HDL particles is compromised in metabolic disorders that have abnormal HDL particle sizes, such as type 2 diabetes mellitus (DM2). By using NMR spectroscopy combined with a biochemical volumetric model we determined the size and spatial lipid distribution of HDL subclasses in a cohort of 26 controls and 29 DM2 patients before and after two drug treatments, one with niacin plus laropiprant and another with fenofibrate as an add-on to simvastatin. We further characterized the HDL surface properties using atomic force microscopy and fluorescent probes to show an abnormal lipid distribution within smaller HDL particles, a subclass particularly enriched in the DM2 patients. The reduction in the size, force cholesterol esters and triglycerides to emerge from the HDL core to the surface, making the outer surface of HDL more hydrophobic. Interestingly, pharmacological interventions had no effect on this undesired configuration, which may explain the lack of clinical benefits in DM2 subjects.
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spelling pubmed-47261052016-01-27 Lipoprotein hydrophobic core lipids are partially extruded to surface in smaller HDL: “Herniated” HDL, a common feature in diabetes Amigó, Núria Mallol, Roger Heras, Mercedes Martínez-Hervás, Sergio Blanco-Vaca, Francisco Escolà-Gil, Joan Carles Plana, Núria Yanes, Óscar Masana, Lluís Correig, Xavier Sci Rep Article Recent studies have shown that pharmacological increases in HDL cholesterol concentrations do not necessarily translate into clinical benefits for patients, raising concerns about its predictive value for cardiovascular events. Here we hypothesize that the size-modulated lipid distribution within HDL particles is compromised in metabolic disorders that have abnormal HDL particle sizes, such as type 2 diabetes mellitus (DM2). By using NMR spectroscopy combined with a biochemical volumetric model we determined the size and spatial lipid distribution of HDL subclasses in a cohort of 26 controls and 29 DM2 patients before and after two drug treatments, one with niacin plus laropiprant and another with fenofibrate as an add-on to simvastatin. We further characterized the HDL surface properties using atomic force microscopy and fluorescent probes to show an abnormal lipid distribution within smaller HDL particles, a subclass particularly enriched in the DM2 patients. The reduction in the size, force cholesterol esters and triglycerides to emerge from the HDL core to the surface, making the outer surface of HDL more hydrophobic. Interestingly, pharmacological interventions had no effect on this undesired configuration, which may explain the lack of clinical benefits in DM2 subjects. Nature Publishing Group 2016-01-18 /pmc/articles/PMC4726105/ /pubmed/26778677 http://dx.doi.org/10.1038/srep19249 Text en Copyright © 2016, Macmillan Publishers Limited 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
Amigó, Núria
Mallol, Roger
Heras, Mercedes
Martínez-Hervás, Sergio
Blanco-Vaca, Francisco
Escolà-Gil, Joan Carles
Plana, Núria
Yanes, Óscar
Masana, Lluís
Correig, Xavier
Lipoprotein hydrophobic core lipids are partially extruded to surface in smaller HDL: “Herniated” HDL, a common feature in diabetes
title Lipoprotein hydrophobic core lipids are partially extruded to surface in smaller HDL: “Herniated” HDL, a common feature in diabetes
title_full Lipoprotein hydrophobic core lipids are partially extruded to surface in smaller HDL: “Herniated” HDL, a common feature in diabetes
title_fullStr Lipoprotein hydrophobic core lipids are partially extruded to surface in smaller HDL: “Herniated” HDL, a common feature in diabetes
title_full_unstemmed Lipoprotein hydrophobic core lipids are partially extruded to surface in smaller HDL: “Herniated” HDL, a common feature in diabetes
title_short Lipoprotein hydrophobic core lipids are partially extruded to surface in smaller HDL: “Herniated” HDL, a common feature in diabetes
title_sort lipoprotein hydrophobic core lipids are partially extruded to surface in smaller hdl: “herniated” hdl, a common feature in diabetes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726105/
https://www.ncbi.nlm.nih.gov/pubmed/26778677
http://dx.doi.org/10.1038/srep19249
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