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Predictive value of HDL function in patients with coronary artery disease: relationship with coronary plaque characteristics and clinical events

BACKGROUND: HDL is endowed with several metabolic, vascular, and immunoinflammatory protective functions. Among them, a key property is to promote reverse cholesterol transport from cells back to the liver. The aim of this study was to estimate the association of scavenger receptor class B type I (S...

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Autores principales: Magnoni, Marco, Andreini, Daniele, Pirillo, Angela, Uboldi, Patrizia, Latini, Roberto, Catapano, Alberico L., Maggioni, Aldo P., Norata, Giuseppe D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090377/
https://www.ncbi.nlm.nih.gov/pubmed/35438019
http://dx.doi.org/10.1080/07853890.2022.2063374
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author Magnoni, Marco
Andreini, Daniele
Pirillo, Angela
Uboldi, Patrizia
Latini, Roberto
Catapano, Alberico L.
Maggioni, Aldo P.
Norata, Giuseppe D.
author_facet Magnoni, Marco
Andreini, Daniele
Pirillo, Angela
Uboldi, Patrizia
Latini, Roberto
Catapano, Alberico L.
Maggioni, Aldo P.
Norata, Giuseppe D.
author_sort Magnoni, Marco
collection PubMed
description BACKGROUND: HDL is endowed with several metabolic, vascular, and immunoinflammatory protective functions. Among them, a key property is to promote reverse cholesterol transport from cells back to the liver. The aim of this study was to estimate the association of scavenger receptor class B type I (SR-BI)- and ATP binding cassette transporter A1 (ABCA1)-mediated cholesterol efflux (the two major routes for cholesterol efflux to HDL) with the presence, extent, and severity of coronary artery disease (CAD), vascular wall remodelling processes, coronary plaque characteristics, and the incidence of myocardial infarction in the different subgroups of patients from the CAPIRE study. METHODS: Patients (n = 525) from the CAPIRE study were divided into two groups: low-risk factors (RF), with 0–1 RF (n = 263), and multiple-RF, with ≥2 RFs; within each group, subjects were classified as no-CAD or CAD based on the segment involvement score (SIS) evaluated by coronary computed tomography angiography (SIS = 0 and SIS > 5, respectively). SR-BI- and ABCA1-mediated cholesterol efflux were measured using the plasma of all patients. RESULTS: SR-BI-mediated cholesterol efflux was significantly reduced in patients with CAD in both the low-RF and multiple-RF groups, whereas ABCA1-mediated cholesterol efflux was similar among all groups. In CAD patients, multivariable analysis showed that SR-BI-mediated cholesterol efflux <25(th) percentile predicted cardiovascular outcome (odds ratio 4.1; 95% CI: 1.3–13.7; p = .019), whereas ABCA-1-mediated cholesterol efflux and HDL-C levels significantly did not. Despite this finding, reduced SR-BI-mediated cholesterol efflux was not associated with changes in high-risk plaque features or changes in the prevalence of elevated total, non-calcified, and low-attenuation plaque volume. CONCLUSION: KEY MESSAGES: Increased cholesterol efflux capacity, an estimate of HDL function, is associated with a reduced CVD risk, regardless of HDL-C levels. HDL-C levels are significantly lower in patients with CAD. Lower SR-BI-mediated cholesterol efflux capacity is observed in patients with diffuse coronary atherosclerosis and is associated with the worst clinical outcomes in patients with CAD, independently of atherosclerotic plaque features.
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spelling pubmed-90903772022-05-11 Predictive value of HDL function in patients with coronary artery disease: relationship with coronary plaque characteristics and clinical events Magnoni, Marco Andreini, Daniele Pirillo, Angela Uboldi, Patrizia Latini, Roberto Catapano, Alberico L. Maggioni, Aldo P. Norata, Giuseppe D. Ann Med Cardiology & Cardiovascular Disorders BACKGROUND: HDL is endowed with several metabolic, vascular, and immunoinflammatory protective functions. Among them, a key property is to promote reverse cholesterol transport from cells back to the liver. The aim of this study was to estimate the association of scavenger receptor class B type I (SR-BI)- and ATP binding cassette transporter A1 (ABCA1)-mediated cholesterol efflux (the two major routes for cholesterol efflux to HDL) with the presence, extent, and severity of coronary artery disease (CAD), vascular wall remodelling processes, coronary plaque characteristics, and the incidence of myocardial infarction in the different subgroups of patients from the CAPIRE study. METHODS: Patients (n = 525) from the CAPIRE study were divided into two groups: low-risk factors (RF), with 0–1 RF (n = 263), and multiple-RF, with ≥2 RFs; within each group, subjects were classified as no-CAD or CAD based on the segment involvement score (SIS) evaluated by coronary computed tomography angiography (SIS = 0 and SIS > 5, respectively). SR-BI- and ABCA1-mediated cholesterol efflux were measured using the plasma of all patients. RESULTS: SR-BI-mediated cholesterol efflux was significantly reduced in patients with CAD in both the low-RF and multiple-RF groups, whereas ABCA1-mediated cholesterol efflux was similar among all groups. In CAD patients, multivariable analysis showed that SR-BI-mediated cholesterol efflux <25(th) percentile predicted cardiovascular outcome (odds ratio 4.1; 95% CI: 1.3–13.7; p = .019), whereas ABCA-1-mediated cholesterol efflux and HDL-C levels significantly did not. Despite this finding, reduced SR-BI-mediated cholesterol efflux was not associated with changes in high-risk plaque features or changes in the prevalence of elevated total, non-calcified, and low-attenuation plaque volume. CONCLUSION: KEY MESSAGES: Increased cholesterol efflux capacity, an estimate of HDL function, is associated with a reduced CVD risk, regardless of HDL-C levels. HDL-C levels are significantly lower in patients with CAD. Lower SR-BI-mediated cholesterol efflux capacity is observed in patients with diffuse coronary atherosclerosis and is associated with the worst clinical outcomes in patients with CAD, independently of atherosclerotic plaque features. Taylor & Francis 2022-04-19 /pmc/articles/PMC9090377/ /pubmed/35438019 http://dx.doi.org/10.1080/07853890.2022.2063374 Text en © 2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cardiology & Cardiovascular Disorders
Magnoni, Marco
Andreini, Daniele
Pirillo, Angela
Uboldi, Patrizia
Latini, Roberto
Catapano, Alberico L.
Maggioni, Aldo P.
Norata, Giuseppe D.
Predictive value of HDL function in patients with coronary artery disease: relationship with coronary plaque characteristics and clinical events
title Predictive value of HDL function in patients with coronary artery disease: relationship with coronary plaque characteristics and clinical events
title_full Predictive value of HDL function in patients with coronary artery disease: relationship with coronary plaque characteristics and clinical events
title_fullStr Predictive value of HDL function in patients with coronary artery disease: relationship with coronary plaque characteristics and clinical events
title_full_unstemmed Predictive value of HDL function in patients with coronary artery disease: relationship with coronary plaque characteristics and clinical events
title_short Predictive value of HDL function in patients with coronary artery disease: relationship with coronary plaque characteristics and clinical events
title_sort predictive value of hdl function in patients with coronary artery disease: relationship with coronary plaque characteristics and clinical events
topic Cardiology & Cardiovascular Disorders
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090377/
https://www.ncbi.nlm.nih.gov/pubmed/35438019
http://dx.doi.org/10.1080/07853890.2022.2063374
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