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dc.rights.licenseopenen_US
dc.contributor.authorSANCHEZ, Manuel
dc.contributor.authorKANNENGIESSER, Caroline
dc.contributor.authorHOANG, Sophie
dc.contributor.authorPOTIER, Louis
dc.contributor.authorFUMERON, Frédéric
dc.contributor.authorVENTECLEF, Nicolas
dc.contributor.authorSCHEEN, André
dc.contributor.authorGAUTIER, Jean-François
dc.contributor.authorHADJADJ, Samy
dc.contributor.authorMARRE, Michel
dc.contributor.authorROUSSEL, Ronan
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorMOHAMMEDI, Kamel
dc.contributor.authorVELHO, Gilberto
dc.date.accessioned2023-03-03T11:26:37Z
dc.date.available2023-03-03T11:26:37Z
dc.date.issued2022-10-11
dc.identifier.issn1475-2840en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/172155
dc.description.abstractEnType 1 diabetes is associated with accelerated vascular aging and advanced atherosclerosis resulting in increased rates of cardiovascular disease and premature death. We evaluated associations between Leukocyte telomere length (LTL), allelic variations (SNPs) in LTL-related genes and the incidence of coronary heart disease (CHD) in adults with long-standing type 1 diabetes. We assessed associations of LTL, measured at baseline by RT-PCR, and of SNPs in 11 LTL-related genes with the risk of coronary heart disease (CHD: myocardial infarction or coronary revascularization) and all-cause death during follow-up in two multicenter French-Belgian prospective cohorts of people with long-standing type 1 diabetes. In logistic and Cox analyses, the lowest tertile of LTL distribution (short telomeres) at baseline was associated with the prevalence of myocardial infarction at baseline and with increased risk of CHD (Hazard ratio 3.14 (1.39-7.70), p = 0.005, for shorter vs longer tertile of LTL) and all-cause death (Hazard ratio 1.63 (95% CI 1.04-2.55), p = 0.03, for shorter vs combined intermediate and longer tertiles of LTL) during follow-up. Allelic variations in six genes related to telomere biology (TERC, NAF1, TERT, TNKS, MEN1 and BICD1) were also associated with the incidence of CHD during follow-up. The associations were independent of sex, age, duration of diabetes, and a range of relevant confounding factors at baseline. Our results suggest that short LTL is an independent risk factor for CHD in people with type 1 diabetes.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enAdaptor Proteins
dc.subject.enSignal Transducing
dc.subject.enAdult
dc.subject.enCoronary Disease
dc.subject.enCytoskeletal Proteins
dc.subject.enDiabetes Mellitus
dc.subject.enType 1
dc.subject.enHumans
dc.subject.enLeukocytes
dc.subject.enMyocardial Infarction
dc.subject.enProspective Studies
dc.subject.enTelomere
dc.title.enLeukocyte telomere length, allelic variations in related genes and risk of coronary heart disease in people with long-standing type 1 diabetes.
dc.title.alternativeCardiovasc Diabetolen_US
dc.typeArticle de revueen_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed36221106en_US
bordeaux.journalCardiovascular Diabetologyen_US
bordeaux.page206en_US
bordeaux.volume21en_US
bordeaux.hal.laboratoriesBiologie des maladies cardiovasculaires (BMC) - UMR 1034en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04013225
hal.version1
hal.date.transferred2023-03-03T11:26:41Z
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccCC BYen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Cardiovascular%20Diabetology&rft.date=2022-10-11&rft.volume=21&rft.issue=1&rft.spage=206&rft.epage=206&rft.eissn=1475-2840&rft.issn=1475-2840&rft.au=SANCHEZ,%20Manuel&KANNENGIESSER,%20Caroline&HOANG,%20Sophie&POTIER,%20Louis&FUMERON,%20Fr%C3%A9d%C3%A9ric&rft.genre=article


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