Publication : Early development of calcific aortic valve disease and left ventricular hypertrophy in a mouse model of combined dyslipidemia and type 2 diabetes mellitus.
bul.description.provenance | ec | fr_CA |
bul.description.provenance | spb | fr_CA |
bul.rights.dateAccepPubl | 2014-08-14 | fr_CA |
bul.rights.periodeEmbargo | forever | fr_CA |
bul.rights.raisonEmbargoInfini | Pour que le document soit diffusé en libre accès, en accord avec le délai prescrit par l’éditeur de Arteriosclerosis, thrombosis, and vascular biology, il faudrait déposer la version acceptée par le comité de lecture, incluant toutes les corrections, sans la mise en page de la revue. Pour ce faire, effectuez une demande de modification à l’aide de la liste des dépôts diffusés à partir du tableau de suivi. | fr_CA |
bul.rights.typeDate | datePublication | fr_CA |
dc.audience | Professeurs (Enseignement supérieur) | fr_CA |
dc.audience | Étudiants | fr_CA |
dc.audience | Doctorants | fr_CA |
dc.audience | Cardiologues | fr_CA |
dc.contributor.author | Lachance, Dominic. | |
dc.contributor.author | Bouchareb, Rihab | |
dc.contributor.author | Kohen Avramoglu, Rita | |
dc.contributor.author | Fournier, Dominique | |
dc.contributor.author | Marette, André | |
dc.contributor.author | Boulanger, Marie-Chloé | |
dc.contributor.author | Le Quang, Khai | |
dc.contributor.author | El Husseini, Diala | |
dc.contributor.author | Fang, Xiang Ping | |
dc.contributor.author | Pibarot, Philippe | |
dc.contributor.author | Deshaies, Yves | |
dc.contributor.author | Sweeney, Gary | |
dc.contributor.author | Mathieu, Patrick | |
dc.contributor.author | Laplante, Marc André | |
dc.date.accessioned | 2016-06-20T18:26:14Z | |
dc.date.available | 9999-12-31 | |
dc.date.issued | 2014-08-14 | |
dc.description.abstract | Objective—This study aimed to determine the potential impact of type 2 diabetes mellitus on left ventricular dysfunction and the development of calcified aortic valve disease using a dyslipidemic mouse model prone to developing type 2 diabetes mellitus. Approach and Results—When compared with nondiabetic LDLr-/-/ApoB100/100, diabetic LDLr-/-/ApoB100/100/IGF-II mice exhibited similar dyslipidemia and obesity but developed type 2 diabetes mellitus when fed a high-fat/sucrose/cholesterol diet for 6 months. LDLr-/-/ApoB100/100/IGF-II mice showed left ventricular hypertrophy versus C57BL6 but not LDLr-/-/ ApoB100/100 mice. Transthoracic echocardiography revealed significant reductions in both left ventricular systolic fractional shortening and diastolic function in high-fat/sucrose/cholesterol fed LDLr-/-/ApoB100/100/IGF-II mice when compared with LDLr-/-/ApoB100/100. Importantly, we found that peak aortic jet velocity was significantly increased in LDLr-/-/ApoB100/100/ IGF-II mice versus LDLr-/-/ApoB100/100 animals on the high-fat/sucrose/cholesterol diet. Microtomography scans and Alizarin red staining indicated calcification in the aortic valves, whereas electron microscopy and energy dispersive x-ray spectroscopy further revealed mineralization of the aortic leaflets and the presence of inflammatory infiltrates in diabetic mice. Studies showed upregulation of hypertrophic genes (anp, bnp, b-mhc) in myocardial tissues and of osteogenic genes (spp1, bglap, runx2) in aortic tissues of diabetic mice. Conclusions—We have established the diabetes mellitus –prone LDLr-/-/ApoB100/100/IGF-II mouse as a new model of calcified aortic valve disease. Our results are consistent with the growing body of clinical evidence that the dysmetabolic state of type 2 diabetes mellitus contributes to early mineralization of the aortic valve and calcified aortic valve disease pathogenesis. | fr_CA |
dc.identifier.doi | 10.1161/ATVBAHA.114.304205 | fr_CA |
dc.identifier.issn | 1079-5642 | fr_CA |
dc.identifier.pubmed | 25231636 | fr_CA |
dc.identifier.uri | http://hdl.handle.net/20.500.11794/6891 | |
dc.language | eng | fr_CA |
dc.publisher | American Heart Association | fr_CA |
dc.rights | http://purl.org/coar/access_right/c_16ec | |
dc.subject | aortic valve stenosis | fr_CA |
dc.subject | diabetes mellitus, type 2 | fr_CA |
dc.subject | inflammation | fr_CA |
dc.subject | obesity | fr_CA |
dc.subject.rvm | Aorte -- Rétrécissement | fr_CA |
dc.subject.rvm | Cœur -- Ventricule gauche -- Hypertrophie | fr_CA |
dc.subject.rvm | Dyslipidémies | fr_CA |
dc.subject.rvm | Diabète non insulinodépendant | fr_CA |
dc.subject.rvm | Obésité | fr_CA |
dc.subject.rvm | Souris (Animal de laboratoire) | fr_CA |
dc.subject.rvm | Insuffisance ventriculaire gauche | fr_CA |
dc.title | Early development of calcific aortic valve disease and left ventricular hypertrophy in a mouse model of combined dyslipidemia and type 2 diabetes mellitus. | fr_CA |
dc.type | article de recherche | |
dc.type.legacy | COAR1_1::Texte::Périodique::Revue::Contribution à un journal::Article::Article de recherche | |
dcterms.bibliographicCitation | Arteriosclerosis, thrombosis, and vascular biology, Vol. 34, 2283-2291 (2014) | fr_CA |
dspace.accessstatus.time | 2023-05-25 18:17:02 | |
dspace.entity.type | Publication | |
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rioxxterms.project | 161971, 245048 | fr_CA |
rioxxterms.project.funder-name | irsc | fr_CA |
rioxxterms.version | Version of Record (VoR) | fr_CA |
rioxxterms.version-of-record | https://doi.org/10.1161/ATVBAHA.114.304205 | fr_CA |
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