Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/30544
Full metadata record
DC FieldValueLanguage
dc.contributor.authorCheurfa, Nadir
dc.contributor.authorDubois-Laforgue, Daniele
dc.contributor.authorFerrarezi, Daniela A. F.
dc.contributor.authorReis, Andre F. [UNIFESP]
dc.contributor.authorBrenner, Guilherme M.
dc.contributor.authorBouche, Clara
dc.contributor.authorLe Feuvre, Claude
dc.contributor.authorFumeron, Frederic
dc.contributor.authorTimsit, Jose
dc.contributor.authorMarre, Michel
dc.contributor.authorVelho, Gilberto
dc.date.accessioned2016-01-24T13:49:41Z-
dc.date.available2016-01-24T13:49:41Z-
dc.date.issued2008-04-01
dc.identifierhttp://dx.doi.org/10.2337/db07-1292
dc.identifier.citationDiabetes. Alexandria: Amer Diabetes Assoc, v. 57, n. 4, p. 1063-1068, 2008.
dc.identifier.issn0012-1797
dc.identifier.urihttp://repositorio.unifesp.br/handle/11600/30544-
dc.description.abstractOBJECTIVE-Uncoupling protein 2 (UCP2) is a physiological downregulator of reactive oxygen species generation and plays an antiatherogenic role in the vascular wall. A common variant in the UCP2 promoter (-866G>A) modulates mRNA expression, with increased expression associated with the A allele. We investigated association of this variant with coronary artery disease (CAD) in two cohorts of type 2 diabetic subjects.RESEARCH DESIGN and METHODS-We studied 3,122 subjects from the 6-year prospective Non-Insulin-Dependent Diabetes, Hypertension, Microalbuminuria, Cardiovascular Events, and Ramipril (DIABHYCAR) Study (14.9% of CAD incidence at follow-up). An independent, hospital-based cohort of 335 men, 52% of whom had CAD, was also studied.RESULTS-We observed an inverse association of the A allele with incident cases of CAD in a dominant model (hazard risk 0.88 [95% CI 0.80-0.96]; P = 0.006). Similar results were observed for baseline cases of CAD. Stratification by sex confirmed an allelic association with CAD in men, whereas no association was observed in women. All CAD phenotypes considered-myocardial infarction, angina pectoris, coronary artery bypass graft (CABG), and sudden death-contributed significantly to the association. Results were replicated in a cross-sectional study of an independent cohort (odds ratio 0.47 [95% CI 0.25-0.89]; P = 0.02 for a recessive model).CONCLUSIONS-The A allele of the -866G>A variant of UCP2 was associated with reduced risk of CAD in men with type 2 diabetes in a 6-year prospective study. Decreased risk of myocardial infarction, angina pectoris, CABG, and sudden death contributed individually and significantly to the reduction of CAD risk. This association was independent of other common CAD risk factors.en
dc.format.extent1063-1068
dc.language.isoeng
dc.publisherAmer Diabetes Assoc
dc.relation.ispartofDiabetes
dc.rightsAcesso aberto
dc.titleThe common-866G > A variant in the promoter of UCP2 is associated with decreased risk of coronary artery disease in type 2 diabetic menen
dc.typeArtigo
dc.contributor.institutionINSERM
dc.contributor.institutionCochin Hosp
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.contributor.institutionFed Fac Fdn Med Sci Porto Alegre
dc.contributor.institutionHop La Pitie Salpetriere
dc.contributor.institutionUniv Paris 07
dc.contributor.institutionUniv Paris 05
dc.description.affiliationINSERM, Fac Med Xavier Bichat, U695, F-75018 Paris, France
dc.description.affiliationCochin Hosp, AP HP, Dept Immunol & Diabetol, Paris, France
dc.description.affiliationUniv São Paulo, Lab Cellular & Mol Endocrinol, São Paulo, Brazil
dc.description.affiliationUniversidade Federal de São Paulo, Mol Endocrinol Lab, São Paulo, Brazil
dc.description.affiliationFed Fac Fdn Med Sci Porto Alegre, Post Grad Program Med Sci, Porto Alegre, RS, Brazil
dc.description.affiliationHop La Pitie Salpetriere, Dept Cardiol, AP HP, Paris, France
dc.description.affiliationUniv Paris 07, Paris, France
dc.description.affiliationUniv Paris 05, Paris, France
dc.description.affiliationUnifespUniversidade Federal de São Paulo, Mol Endocrinol Lab, São Paulo, Brazil
dc.identifier.doi10.2337/db07-1292
dc.description.sourceWeb of Science
dc.identifier.wosWOS:000254591700032
Appears in Collections:Em verificação - Geral

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.