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dc.rights.licenseopenen_US
hal.structure.identifierBiologie des maladies cardiovasculaires = Biology of Cardiovascular Diseases
dc.contributor.authorMOHAMMEDI, Kamel
hal.structure.identifierInstitut Necker Enfants-Malades [INEM - UM 111 (UMR 8253 / U1151)]
dc.contributor.authorMARRE, Michel
hal.structure.identifierCentre de Recherche des Cordeliers [CRC (UMR_S_1138 / U1138)]
dc.contributor.authorALHENC-GELAS, François
dc.date.accessioned2025-03-04T12:44:25Z
dc.date.available2025-03-04T12:44:25Z
dc.date.issued2024-12-21
dc.identifier.issn1475-2840en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/205339
dc.description.abstractEnHypertension, cardiovascular disease and kidney failure are associated with persistent hyperglycaemia and the subsequent development of nephropathy in people with diabetes. Diabetic nephropathy is associated with widespread vascular disease affecting both the kidney and the heart from an early stage. However, the risk of diabetic nephropathy in people with type 1 diabetes is strongly genetically determined, as documented in familial transmission studies. The search for the underlying genes has been extensive, using specific hypotheses, sibling linkage studies and genome-wide association studies (GWAS). The role of the angiotensinI-converting enzyme/kininase II (ACE) gene and genetic variability in ACE levels as a susceptibility and prognostic factor for diabetic nephropathy has been well documented in people with type 1 diabetes. The ACE gene insertion/deletion polymorphism, which is associated with plasma and tissue ACE levels, has been the most studied genomic variant in diabetic nephropathy. Recently, this polymorphism has also been associated with longevity in people with type 1 diabetes. The ACE I/D polymorphism has also been associated with vascular, extra-renal complications including myocardial infarction and lower-limb amputation in this population. Other genes and loci have been identified in linkage studies and GWAS, such as the COL4A3 gene or a region on chromosome 3q with the adiponectin gene. Replication was not always attempted and was rarely achieved, even for GWAS. Overall, effect sizes remain modest and no major gene has been identified, despite the strength of the genetic effect in transmission studies. We searched bibliographic databases for studies reporting genomic variants associated with diabetic nephropathy and meta-analyses of such studies. We selected important relevant studies for further discussion in this narrative review. This brief review attempts to summarise the current knowledge on the genetics of diabetic nephropathy and associated cardiovascular disease in people with type 1 diabetes, and discusses some conceptual and methodological issues relevant to the interpretation of past studies and the design of future ones.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enHumans
dc.subject.enGenetic Predisposition to Disease
dc.subject.enDiabetic Nephropathies
dc.subject.enDiabetes Mellitus
dc.subject.enType 1
dc.subject.enPeptidyl-Dipeptidase A
dc.subject.enCardiovascular Diseases
dc.subject.enPhenotype
dc.subject.enGenome-Wide Association Study
dc.subject.enRisk Factors
dc.subject.enPolymorphism
dc.subject.enGenetic
dc.title.enGenetic predisposition to nephropathy and associated cardiovascular disease in people with type 1 diabetes: role of the angiotensinI-converting enzyme (ACE), and beyond; a narrative review.
dc.title.alternativeCardiovasc Diabetolen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1186/s12933-024-02544-0en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed39709470en_US
bordeaux.journalCardiovascular Diabetologyen_US
bordeaux.page453en_US
bordeaux.volume23en_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-04975938
hal.version1
hal.date.transferred2025-03-04T12:44:28Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Cardiovascular%20Diabetology&rft.date=2024-12-21&rft.volume=23&rft.issue=1&rft.spage=453&rft.epage=453&rft.eissn=1475-2840&rft.issn=1475-2840&rft.au=MOHAMMEDI,%20Kamel&MARRE,%20Michel&ALHENC-GELAS,%20Fran%C3%A7ois&rft.genre=article


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