Affiliation:
1. From the Division of Cardiovascular Genetics, Department of Medicine, The Rayne Institute, University College London, UK (D.M.W., J.R., S.E.H., P.T.); Hospital Broussais, Paris, France (V.N.); and Institute Pasteur, Lille, France (J.D.).
Abstract
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 (OFTT) 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 (
Sst
I) 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% AUC,
P
=0.013) and insulin (20.5% AUC,
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.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Cited by
79 articles.
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