ApoCIII gene variants modulate postprandial response to both glucose and fat tolerance tests

被引:81
作者
Waterworth, DM
Ribalta, J
Nicaud, V
Dallongeville, J
Humphries, SE
Talmud, P
机构
[1] Univ London Univ Coll, Rayne Inst, Dept Med, Div Cardiovasc Genet, London WC1E 6JJ, England
[2] Hop Broussais, Paris, France
[3] Inst Pasteur, Paris, France
关键词
genes; apolipoproteins; diet;
D O I
10.1161/01.CIR.99.14.1872
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-We investigated the relationship between variation in the apolipoprotein (apo) AI-CIII-AIV gene cluster and response to an oral glucose test (OGTT) and oral fat load test (OFPT) in the EARSII group of young, healthy male offspring whose fathers had had a myocardial infarction before the age of 55 years (cases, n=407) compared with age-matched controls (n=415). The apoCIII variations examined were C3238G (SstI) in the 3'-UTR, C1100T in exon 3, C-482T in the insulin response element (IRE), and T-2854G in the apoCIII-AIV intergenic region. Methods and Results-The postprandial response was regulated by variation at the T-2854G and C3238G sites. After the OFTT, carriers of the rare alleles had delayed clearance of triglyceride (Tg) levels; G-2854 carriers showed the largest effect on Tg (AUC, 24%; greater, P<0.002; peak, 19% greater, P<0.005), and G3238 carriers showed a smaller response (AUC, 13% greater, P<0.05; peak, 13% greater, P=0.03). However, after adjustment for fasting level of Tg, only the effect with the T-2854G remained significant. Variation at the C-482T (IRE) determined response to the OGTT, with carriers of the rare T-482 having significantly elevated glucose (28.7% AUG, P=0.013) and insulin (20.5% AUG, P<0.01) concentrations. Conclusions-These data suggest that specific genetic variants at the apoCIII gene locus differentially affect postprandial and response to OGTT and suggest a novel mechanism for the effects of variation at this locus on risk for atherosclerosis.
引用
收藏
页码:1872 / 1877
页数:6
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