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Role of HDL function and LDL atherogenicity on cardiovascular risk: A comprehensive examination

dc.contributor.authorHernaez, Alvaro
dc.contributor.authorSoria-Florido, Maria Trinidad
dc.contributor.authorSchroder, Helmut
dc.contributor.authorRos, Emilio
dc.contributor.authorPinto, Xavier
dc.contributor.authorEstruch, Ramon
dc.contributor.authorSalas-Salvado, Jordi
dc.contributor.authorCorella, Dolores
dc.contributor.authorAros, Fernando
dc.contributor.authorSerra-Majem, Lluis
dc.contributor.authorMartinez-Gonzalez, Miguel Angel
dc.contributor.authorFiol Sala, Miquel
dc.contributor.authorLapetra, Jose
dc.contributor.authorElosua, Roberto
dc.contributor.authorLamuela-Raventos, Rosa María
dc.contributor.authorFito, Montserrat
dc.date.accessioned2024-09-10T13:10:30Z
dc.date.available2024-09-10T13:10:30Z
dc.date.issued2019-06-27
dc.description.abstractBackground: High-density lipoprotein (HDL) functionality and low-density lipoprotein (LDL) atherogenic traits can describe the role of both particles on cardiovascular diseases more accurately than HDL- or LDL-cholesterol levels. However, it is unclear how these lipoprotein properties are particularly affected by different cardiovascular risk factors. Objective: To determine which lipoprotein properties are associated with greater cardiovascular risk scores and each cardiovascular risk factor. Methods: In two cross-sectional baseline samples of PREDIMED trial volunteers, we assessed the associations of HDL functionality (N = 296) and LDL atherogenicity traits (N = 210) with: 1) the 10-year predicted coronary risk (according to the Framingham-REGICOR score), and 2) classical cardiovascular risk factors. Results Greater cardiovascular risk scores were associated with low cholesterol efflux values; oxidized, triglyceride-rich, small HDL particles; and small LDLs with low resistance against oxidation (P-trend<0.05, all). After adjusting for the rest of risk factors; 1) type-2 diabetic individuals presented smaller and more oxidized LDLs (P<0.026, all); 2) dyslipidemic participants had smaller HDLs with an impaired capacity to metabolize cholesterol (P<0.035, all); 3) high body mass index values were associated to lower HDL and LDL size and a lower HDL capacity to esterify cholesterol (P<0.037, all); 4) men presented a greater HDL oxidation and lower HDL vasodilatory capacity (P<0.046, all); and 5) greater ages were related to small, oxidized, cytotoxic LDL particles (P<0.037, all). Conclusions: Dysfunctional HDL and atherogenic LDL particles are present in high cardiovascular risk patients. Dyslipidemia and male sex are predominantly linked to HDL dysfunctionality, whilst diabetes and advanced age are associated with LDL atherogenicity.en
dc.description.sponsorshipThis work was supported by: Agencia de Gestio d'Ajuts Universitaris i de Recerca (2017 SGR 222), Fundacio La Marato de TV3 (201512.31), and Instituto de Salud Carlos III (CB06/03/0028 and PI15/00047). A.H. was funded by Instituto de Salud Carlos III (CD17/00122), M.-T.S.-F. was supported by Agencia de Gestio d'Ajuts Universitaris i de Recerca (2015 FI_B 01042), and M. Fito was supported by Instituto de Salud Carlos III (CES12/025). CIBERs of Pathophysiology of Obesity and Nutrition (CIBEROBN) and Cardiovascular Diseases (CIBERCV) are initiatives of the Instituto de Salud Carlos III, Madrid, Spain. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.es_ES
dc.format.number6es_ES
dc.format.pagee0218533es_ES
dc.format.volume14es_ES
dc.identifier.citationHernaez A, Soria-Florido MT, Schroder H, Ros E, Pinto X, Estruch R, et al. Role of HDL function and LDL atherogenicity on cardiovascular risk: A comprehensive examination. PLoS One. 2019 Jun 27;14(6):e0218533.en
dc.identifier.doi10.1371/journal.pone.0218533
dc.identifier.issn1932-6203
dc.identifier.journalPloS Onees_ES
dc.identifier.otherhttp://hdl.handle.net/20.500.13003/16275
dc.identifier.pubmedID31246976es_ES
dc.identifier.puiL2002368447
dc.identifier.scopus2-s2.0-85068971562
dc.identifier.urihttps://hdl.handle.net/20.500.12105/22795
dc.identifier.wos484911900027
dc.language.isoengen
dc.publisherPublic Library of Science (PLOS)
dc.relation.publisherversionhttps://dx.doi.org/10.1371/journal.pone.0218533en
dc.rights.accessRightsopen accessen
dc.rights.licenseAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.decsLDL-Colesterol*
dc.subject.decsFemenino*
dc.subject.decsLipoproteínas HDL*
dc.subject.decsHDL-Colesterol*
dc.subject.decsLipoproteínas LDL*
dc.subject.decsMasculino*
dc.subject.decsAterosclerosis*
dc.subject.decsFactores Sexuales*
dc.subject.decsEstudios Transversales*
dc.subject.decsFactores de Riesgo*
dc.subject.decsDislipidemias*
dc.subject.decsHumanos*
dc.subject.decsPersona de Mediana Edad*
dc.subject.decsFactores de Edad*
dc.subject.decsAnciano*
dc.subject.decsDiabetes Mellitus Tipo 2*
dc.subject.decsEnfermedades Cardiovasculares*
dc.subject.decsAdulto*
dc.subject.meshCardiovascular Diseases*
dc.subject.meshDiabetes Mellitus, Type 2*
dc.subject.meshAged*
dc.subject.meshAge Factors*
dc.subject.meshAdult*
dc.subject.meshHumans*
dc.subject.meshMiddle Aged*
dc.subject.meshCross-Sectional Studies*
dc.subject.meshLipoproteins, LDL*
dc.subject.meshMale*
dc.subject.meshCholesterol, LDL*
dc.subject.meshLipoproteins, HDL*
dc.subject.meshSex Factors*
dc.subject.meshCholesterol, HDL*
dc.subject.meshDyslipidemias*
dc.subject.meshFemale*
dc.subject.meshRisk Factors*
dc.subject.meshAtherosclerosis*
dc.titleRole of HDL function and LDL atherogenicity on cardiovascular risk: A comprehensive examinationen
dc.typeresearch articleen
dspace.entity.typePublication
relation.isPublisherOfPublicationa2759e3d-0d58-4e8a-9fcd-c6130ee333d1
relation.isPublisherOfPublication.latestForDiscoverya2759e3d-0d58-4e8a-9fcd-c6130ee333d1

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