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Interaction of the common apolipoprotein C-III (APOC3 -482C > T) and hepatic lipase (LIPC -514C > T) promoter variants affects glucose tolerance in young adults. European Atherosclerosis Research Study II (EARS-II)

Published online by Cambridge University Press:  26 June 2001

H. JANSEN
Affiliation:
Departments of Internal Medicine, Biochemistry and Clinical Chemistry, Erasmus University, POB 1738, 3000 DR Rotterdam, The Netherlands
D. M. WATERWORTH
Affiliation:
Department of Medicine, Rayne Institute, Royal Free and University College Medical School, 5 University St, London WC1E 6JJ, UK
V. NICAUD
Affiliation:
INSERM U525, Faculté de Médecine Pitié-Salpêtrière, 91 Bd de l'Hôpital, 75013 Paris, France
C. EHNHOLM
Affiliation:
National Public Health Institute, Department of Biochemistry, Mannerheimintie 166, 00300 Helsinki, Finland
P. J. TALMUD
Affiliation:
Department of Medicine, Rayne Institute, Royal Free and University College Medical School, 5 University St, London WC1E 6JJ, UK
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Abstract

Both hepatic lipase (HL) and apolipoprotein C-III (apoC-III) influence lipid metabolism. Common variation in promoters of both genes, LIPC -514C > T and APOC3 -482C > T, respectively, have been shown to affect plasma lipids and lipoproteins and glucose tolerance. We studied the interaction between both variants on parameters of glucose tolerance and lipid metabolism in 714 healthy young males participating in the second European Atherosclerosis Research Study (EARS-II). Approximately 18% of the subjects were carriers of at least one rare LIPC and APOC3 allele. These subjects exhibited, after fasting and oral fat loading, the highest values of triglyceride-rich lipoproteins, but there was no significant interactive effect on any lipid variable. However, interaction occurred on basal diastolic blood pressure (p =0.036) and, during oral glucose tolerance testing, on peak (p = 0.0065) and area under the curve for glucose (p =0.049), and insulin (p = 0.035). This resulted in the highest diastolic blood pressure and lowest glucose tolerance in carriers of at least one rare allele of both genes. Thus gene:gene interaction between LIPC and APOC3, even in these healthy young males, leads to changes in parameters that are typically characteristic of Syndrome-X.

Type
Research Article
Copyright
© University College London 2001

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