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dc.rights.licenseopenen_US
dc.contributor.authorGELLEN, B.
dc.contributor.authorTHORIN-TRESCASES, N.
dc.contributor.authorTHORIN, E.
dc.contributor.authorGAND, E.
dc.contributor.authorSOSNER, P.
dc.contributor.authorBRISHOUAL, S.
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorRIGALLEAU, Vincent
IDREF: 069788146
dc.contributor.authorMONTAIGNE, D.
dc.contributor.authorJAVAUGUE, V.
dc.contributor.authorPUCHEU, Y.
dc.contributor.authorGATAULT, P.
dc.contributor.authorPIGUEL, X.
dc.contributor.authorHADJADJ, S.
dc.contributor.authorSAULNIER, P. J.
dc.date.accessioned2021-01-26T12:31:28Z
dc.date.available2021-01-26T12:31:28Z
dc.date.issued2020
dc.identifier.issn1432-0428 (Electronic) 0012-186X (Linking)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/26010
dc.description.abstractEnAims/hypothesis: Tenascin-C (TN-C) is an extracellular matrix glycoprotein highly expressed in inflammatory and cardiovascular (CV) diseases. Serum TN-C has not yet been specifically studied in individuals with type 2 diabetes, a condition associated with chronic low-grade inflammation and increased CV disease risk. In this study, we hypothesised that elevated serum TN-C at enrolment in participants with type 2 diabetes would be associated with increased risk of death and major adverse CV events (MACE) during follow-up. Methods: We used a prospective, monocentric cohort of consecutive type 2 diabetes participants (the SURDIAGENE [SUivi Rénal, DIAbète de type 2 et GENEtique] cohort) with all-cause death as a primary endpoint and MACE (CV death, non-fatal myocardial infarction or stroke) as a secondary endpoint. We used a proportional hazard model after adjustment for traditional risk factors and the relative integrated discrimination improvement (rIDI) to assess the incremental predictive value of TN-C for these risk factors. Results: We monitored 1321 individuals (58% men, mean age 64 ± 11 years) for a median of 89 months. During follow-up, 442 individuals died and 497 had MACE. Multivariate Cox analysis showed that serum TN-C concentrations were associated with an increased risk of death (HR per 1 SD: 1.27 [95% CI 1.17, 1.38]; p < 0.0001) and MACE (HR per 1 SD: 1.23 [95% CI 1.13, 1.34]; p < 0.0001). Using TN-C concentrations on top of traditional risk factors, prediction of the risk of all-cause death (rIDI: 8.2%; p = 0.0006) and MACE (rIDI: 6.7%; p = 0.0014) improved significantly, but modestly. Conclusions/interpretation: In individuals with type 2 diabetes, increased serum TN-C concentrations were independently associated with death and MACE. Therefore, including TN-C as a prognostic biomarker could improve risk stratification in these individuals.
dc.language.isoENen_US
dc.subjectLEHA
dc.title.enSerum tenascin-C is independently associated with increased major adverse cardiovascular events and death in individuals with type 2 diabetes: a French prospective cohort
dc.title.alternativeDiabetologiaen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1007/s00125-020-05108-5en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed32040670en_US
bordeaux.journalDiabetologiaen_US
bordeaux.page915-923en_US
bordeaux.volume63en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - U1219en_US
bordeaux.issue5en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.teamLEHA_BPH
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03121403
hal.version1
hal.date.transferred2021-01-26T12:31:33Z
hal.exporttrue
bordeaux.COinSctx_ver=Z39.88-2004&amp;rft_val_fmt=info:ofi/fmt:kev:mtx:journal&amp;rft.jtitle=Diabetologia&amp;rft.date=2020&amp;rft.volume=63&amp;rft.issue=5&amp;rft.spage=915-923&amp;rft.epage=915-923&amp;rft.eissn=1432-0428%20(Electronic)%200012-186X%20(Linking)&amp;rft.issn=1432-0428%20(Electronic)%200012-186X%20(Linking)&amp;rft.au=GELLEN,%20B.&amp;THORIN-TRESCASES,%20N.&amp;THORIN,%20E.&amp;GAND,%20E.&amp;SOSNER,%20P.&amp;rft.genre=article


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