High-density lipoprotein cholesterol efflux capacity and cardiovascular risk in autoimmune and non-autoimmune diseases.

Autoimmune disease Cardiovascular disease (CVD). Cardiovascular risk Cholesterol efflux capacity HDL function HDL-cholesterol High-density lipoprotein (HDL)

Journal

Metabolism: clinical and experimental
ISSN: 1532-8600
Titre abrégé: Metabolism
Pays: United States
ID NLM: 0375267

Informations de publication

Date de publication:
03 2020
Historique:
received: 30 10 2019
revised: 23 12 2019
accepted: 05 01 2020
pubmed: 11 1 2020
medline: 21 4 2020
entrez: 11 1 2020
Statut: ppublish

Résumé

Functional assessment of cholesterol efflux capacity (CEC) to high-density lipoprotein (HDL) is an emerging tool for evaluating morbidity and mortality associated with cardiovascular disease (CVD). By promoting macrophage reverse cholesterol transport (RCT), HDL-mediated CEC is believed to play an important role in atherosclerotic lesion progression in the vessel wall. Furthermore, recent evidence indicates that the typical inverse associations between various forms of CEC and CV events may be strongly modulated by environmental systemic factors and traditional CV risk factors, in addition to autoimmune diseases. These factors influence the complex and dynamic composition of HDL particles, which in turn positively or negatively affect HDL-CEC. Herein, we review recent findings connecting HDL-CEC to traditional CV risk factors and cardiometabolic conditions (non-autoimmune diseases) as well as autoimmune diseases, with a specific focus on how these factors may influence the associations between HDL-CEC and CVD risk.

Identifiants

pubmed: 31923386
pii: S0026-0495(20)30005-6
doi: 10.1016/j.metabol.2020.154141
pii:
doi:

Substances chimiques

Cholesterol, HDL 0
Lipoproteins, HDL 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

154141

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest AH, EF, SSD and MAF have no conflict of interest to declare. NV received restricted research grants from Roche.

Auteurs

Anouar Hafiane (A)

Department of Medicine, Faculty of Medicine, Research Institute of the McGill University Health Centre, McGill University, 1001 Decarie Blvd, Bloc E01. 3370H, Montréal, Qc H4A 3J1, Canada. Electronic address: anouar.hafiane@mail.mcgill.ca.

Elda Favari (E)

Department of Food and Drug, University of Parma, Parco Area delle Scienze, 27/A, 43124 Parma, Italy. Electronic address: elda.favari@unipr.it.

Stella S Daskalopoulou (SS)

Department of Medicine, Division of Internal Medicine, McGill University, Research Institute of the McGill University Health Centre, 1001 Decarie Blvd, EM1.2230, Montreal, Quebec H4A 3J1, Canada. Electronic address: stella.daskalopoulou@mcgill.ca.

Nicolas Vuilleumier (N)

Division of Laboratory Medicine, Diagnostic Department, Geneva University Hospitals, 1211 Geneva, Switzerland; Division of Laboratory Medicine, Department of Medical Specialties, Faculty of Medicine, University of Geneva, 1206 Geneva, Switzerland. Electronic address: nicolas.vuilleumier@hcuge.ch.

Miguel A Frias (MA)

Division of Laboratory Medicine, Diagnostic Department, Geneva University Hospitals, 1211 Geneva, Switzerland; Division of Laboratory Medicine, Department of Medical Specialties, Faculty of Medicine, University of Geneva, 1206 Geneva, Switzerland. Electronic address: miguel.frias@hcuge.ch.

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Classifications MeSH