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http://purl.uniprot.org/citations/17666459http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/17666459http://www.w3.org/2000/01/rdf-schema#comment"

Objective

Type 2 diabetic patients have a high risk of coronary heart disease (CHD) and sudden death. This cardiovascular risk can be partly attributed to low levels of HDL cholesterol. The B2 allele of the CETP TaqIB polymorphism has been repeatedly reported to be associated with high HDL cholesterol levels in both healthy and type 2 diabetic subjects, but its association with CHD is unclear. We investigated the association of the CETP TaqIB polymorphism with CHD, and sudden death in particular, in a prospective cohort of type 2 diabetic patients.

Research design and methods

The CETP TaqIB polymorphism was genotyped in 3,124 type 2 diabetic subjects with high cardiovascular risk: the Noninsulin-Dependent Diabetes, Hypertension, Microalbuminuria, Proteinuria, Cardiovascular Events, and Ramipril (DIABHYCAR) study. We used Cox regression analysis to estimate the impact of the TaqIB single nucleotide polymorphism on the CHD events (myocardial infarction or sudden death) during follow-up.

Results

The incidence of CHD was higher in B1B1 homozygotes than in B2 carriers (P = 0.02). This effect was mainly due to sudden death (hazard ratio [B1B1 vs. B2+] = 1.51 [95% CI = 1.05-2.18]). Although the B1 allele was associated in a dose-dependent fashion with lower HDL cholesterol (P < 0.001), the association with sudden death persisted after adjustment for multiple risk factors, including HDL cholesterol levels.

Conclusions

In type 2 diabetic patients, the CETP TaqIB polymorphism is a good genetic predictor of cardiac mortality. This association is partly independent of the effect on HDL cholesterol levels."xsd:string
http://purl.uniprot.org/citations/17666459http://purl.org/dc/terms/identifier"doi:10.2337/dc07-0869"xsd:string
http://purl.uniprot.org/citations/17666459http://purl.uniprot.org/core/author"Fumeron F."xsd:string
http://purl.uniprot.org/citations/17666459http://purl.uniprot.org/core/author"Marre M."xsd:string
http://purl.uniprot.org/citations/17666459http://purl.uniprot.org/core/author"Pean F."xsd:string
http://purl.uniprot.org/citations/17666459http://purl.uniprot.org/core/author"Bellili N."xsd:string
http://purl.uniprot.org/citations/17666459http://purl.uniprot.org/core/author"Jaziri R."xsd:string
http://purl.uniprot.org/citations/17666459http://purl.uniprot.org/core/author"Porchay-Balderelli I."xsd:string
http://purl.uniprot.org/citations/17666459http://purl.uniprot.org/core/date"2007"xsd:gYear
http://purl.uniprot.org/citations/17666459http://purl.uniprot.org/core/name"Diabetes Care"xsd:string
http://purl.uniprot.org/citations/17666459http://purl.uniprot.org/core/pages"2863-2867"xsd:string
http://purl.uniprot.org/citations/17666459http://purl.uniprot.org/core/title"The CETP TaqIB polymorphism is associated with the risk of sudden death in type 2 diabetic patients."xsd:string
http://purl.uniprot.org/citations/17666459http://purl.uniprot.org/core/volume"30"xsd:string
http://purl.uniprot.org/citations/17666459http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/17666459
http://purl.uniprot.org/citations/17666459http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/17666459
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