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Association of HDL cholesterol efflux capacity with incident coronary heart disease events: a prospective case-control study

BACKGROUND: Although HDL cholesterol concentrations are strongly and inversely associated with risk of coronary heart disease, interventions that raise HDL cholesterol do not reduce risk of coronary heart disease. HDL cholesterol efflux capacity—a prototypical measure of HDL function—has been associ...

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Autores principales: Saleheen, Danish, Scott, Robert, Javad, Sundas, Zhao, Wei, Rodrigues, Amrith, Picataggi, Antonino, Lukmanova, Daniya, Mucksavage, Megan L, Luben, Robert, Billheimer, Jeffery, Kastelein, John J P, Boekholdt, S Matthijs, Khaw, Kay-Tee, Wareham, Nick, Rader, Daniel J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Lancet, Diabetes & Endocrinology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648056/
https://www.ncbi.nlm.nih.gov/pubmed/26025389
http://dx.doi.org/10.1016/S2213-8587(15)00126-6
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author Saleheen, Danish
Scott, Robert
Javad, Sundas
Zhao, Wei
Rodrigues, Amrith
Picataggi, Antonino
Lukmanova, Daniya
Mucksavage, Megan L
Luben, Robert
Billheimer, Jeffery
Kastelein, John J P
Boekholdt, S Matthijs
Khaw, Kay-Tee
Wareham, Nick
Rader, Daniel J
author_facet Saleheen, Danish
Scott, Robert
Javad, Sundas
Zhao, Wei
Rodrigues, Amrith
Picataggi, Antonino
Lukmanova, Daniya
Mucksavage, Megan L
Luben, Robert
Billheimer, Jeffery
Kastelein, John J P
Boekholdt, S Matthijs
Khaw, Kay-Tee
Wareham, Nick
Rader, Daniel J
author_sort Saleheen, Danish
collection PubMed
description BACKGROUND: Although HDL cholesterol concentrations are strongly and inversely associated with risk of coronary heart disease, interventions that raise HDL cholesterol do not reduce risk of coronary heart disease. HDL cholesterol efflux capacity—a prototypical measure of HDL function—has been associated with coronary heart disease after adjusting for HDL cholesterol, but its effect on incident coronary heart disease risk is uncertain. METHODS: We measured cholesterol efflux capacity and assessed its relation with vascular risk factors and incident coronary heart disease events in a nested case-control sample from the prospective EPIC-Norfolk study of 25 639 individuals aged 40–79 years, assessed in 1993–97 and followed up to 2009. We quantified cholesterol efflux capacity in 1745 patients with incident coronary heart disease and 1749 control participants free of any cardiovascular disorders by use of a validated ex-vivo radiotracer assay that involved incubation of cholesterol-labelled J774 macrophages with apoB-depleted serum from study participants. FINDINGS: Cholesterol efflux capacity was positively correlated with HDL cholesterol concentration (r=0·40; p<0·0001) and apoA-I concentration (r=0·22; p<0·0001). It was also inversely correlated with type 2 diabetes (r=–0·18; p<0·0001) and positively correlated with alcohol consumption (r=0·12; p<0·0001). In analyses comparing the top and bottom tertiles, cholesterol efflux capacity was significantly and inversely associated with incident coronary heart disease events, independent of age, sex, diabetes, hypertension, smoking and alcohol use, waist:hip ratio, BMI, LDL cholesterol concentration, log-triglycerides, and HDL cholesterol or apoA-I concentrations (odds ratio 0·64, 95% CI 0·51–0·80). After a similar multivariable adjustment the risk of incident coronary heart disease was 0·80 (95% CI 0·70–0·90) for a per-SD change in cholesterol efflux capacity. INTERPRETATION: HDL cholesterol efflux capacity might provide an alternative mechanism for therapeutic modulation of the HDL pathway beyond HDL cholesterol concentration to help reduce risk of coronary heart disease. FUNDING: US National Institutes of Health, UK Medical Research Council, Cancer Research UK.
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spelling pubmed-46480562015-12-09 Association of HDL cholesterol efflux capacity with incident coronary heart disease events: a prospective case-control study Saleheen, Danish Scott, Robert Javad, Sundas Zhao, Wei Rodrigues, Amrith Picataggi, Antonino Lukmanova, Daniya Mucksavage, Megan L Luben, Robert Billheimer, Jeffery Kastelein, John J P Boekholdt, S Matthijs Khaw, Kay-Tee Wareham, Nick Rader, Daniel J Lancet Diabetes Endocrinol Articles BACKGROUND: Although HDL cholesterol concentrations are strongly and inversely associated with risk of coronary heart disease, interventions that raise HDL cholesterol do not reduce risk of coronary heart disease. HDL cholesterol efflux capacity—a prototypical measure of HDL function—has been associated with coronary heart disease after adjusting for HDL cholesterol, but its effect on incident coronary heart disease risk is uncertain. METHODS: We measured cholesterol efflux capacity and assessed its relation with vascular risk factors and incident coronary heart disease events in a nested case-control sample from the prospective EPIC-Norfolk study of 25 639 individuals aged 40–79 years, assessed in 1993–97 and followed up to 2009. We quantified cholesterol efflux capacity in 1745 patients with incident coronary heart disease and 1749 control participants free of any cardiovascular disorders by use of a validated ex-vivo radiotracer assay that involved incubation of cholesterol-labelled J774 macrophages with apoB-depleted serum from study participants. FINDINGS: Cholesterol efflux capacity was positively correlated with HDL cholesterol concentration (r=0·40; p<0·0001) and apoA-I concentration (r=0·22; p<0·0001). It was also inversely correlated with type 2 diabetes (r=–0·18; p<0·0001) and positively correlated with alcohol consumption (r=0·12; p<0·0001). In analyses comparing the top and bottom tertiles, cholesterol efflux capacity was significantly and inversely associated with incident coronary heart disease events, independent of age, sex, diabetes, hypertension, smoking and alcohol use, waist:hip ratio, BMI, LDL cholesterol concentration, log-triglycerides, and HDL cholesterol or apoA-I concentrations (odds ratio 0·64, 95% CI 0·51–0·80). After a similar multivariable adjustment the risk of incident coronary heart disease was 0·80 (95% CI 0·70–0·90) for a per-SD change in cholesterol efflux capacity. INTERPRETATION: HDL cholesterol efflux capacity might provide an alternative mechanism for therapeutic modulation of the HDL pathway beyond HDL cholesterol concentration to help reduce risk of coronary heart disease. FUNDING: US National Institutes of Health, UK Medical Research Council, Cancer Research UK. The Lancet, Diabetes & Endocrinology 2015-07 /pmc/articles/PMC4648056/ /pubmed/26025389 http://dx.doi.org/10.1016/S2213-8587(15)00126-6 Text en © 2015 Saleheen et al. Open Acess article disrtibuted under the terms of CC BY-NC-ND http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Articles
Saleheen, Danish
Scott, Robert
Javad, Sundas
Zhao, Wei
Rodrigues, Amrith
Picataggi, Antonino
Lukmanova, Daniya
Mucksavage, Megan L
Luben, Robert
Billheimer, Jeffery
Kastelein, John J P
Boekholdt, S Matthijs
Khaw, Kay-Tee
Wareham, Nick
Rader, Daniel J
Association of HDL cholesterol efflux capacity with incident coronary heart disease events: a prospective case-control study
title Association of HDL cholesterol efflux capacity with incident coronary heart disease events: a prospective case-control study
title_full Association of HDL cholesterol efflux capacity with incident coronary heart disease events: a prospective case-control study
title_fullStr Association of HDL cholesterol efflux capacity with incident coronary heart disease events: a prospective case-control study
title_full_unstemmed Association of HDL cholesterol efflux capacity with incident coronary heart disease events: a prospective case-control study
title_short Association of HDL cholesterol efflux capacity with incident coronary heart disease events: a prospective case-control study
title_sort association of hdl cholesterol efflux capacity with incident coronary heart disease events: a prospective case-control study
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648056/
https://www.ncbi.nlm.nih.gov/pubmed/26025389
http://dx.doi.org/10.1016/S2213-8587(15)00126-6
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