Postprandial responses of individual fatty acids in subjects homozygous for the threonine- or alanine-encoding allele in codon 54 of the intestinal fatty acid binding protein 2 gene
Open Access
- 1 January 2001
- journal article
- research article
- Published by Elsevier in The American Journal of Clinical Nutrition
- Vol. 73 (1) , 31-35
- https://doi.org/10.1093/ajcn/73.1.31
Abstract
Background: The affinity of intestinal fatty acid binding protein (FABP) for fatty acids is regulated by the polymorphism at codon 54 of the FABP2 gene (alanine-to-threonine shift). We found earlier that the threonine-encoding allele (Thr54) is associated with an increased postprandial lipemic response. Objective: We studied the postprandial responses of individual fatty acids in subjects homozygous for the Thr54 or alanine-encoding allele (Ala54). Design: Oral-fat-loading tests were performed in 8 subjects homozygous for Thr54 and in 7 subjects homozygous for Ala54. Results: The postprandial responses of most of the 14–18-carbon fatty acids in chylomicron and VLDL triacylglycerols were significantly elevated in the Thr54 homozygotes whereas the relative increases in these fatty acids were not significantly different in both groups. The amounts of 20- and 22-carbon polyunsaturated fatty acids started to increase later than the amounts of shorter ones after the test meal, and the differences between the groups were mostly insignificant. The responses of chylomicron fatty acids correlated positively with postprandial insulin response in the Thr54 homozygotes and inversely in the Ala54 homozygotes. VLDL fatty acid responses correlated with fasting triacylglycerol concentrations in the Ala54 homozygotes but not in the Thr54 homozygotes. Conclusion: The threonine-encoding allele of the FABP2 gene is associated with an increased postprandial response of 14–18-carbon fatty acids but not with changes in the relative amounts of individual fatty acids introduced to chylomicron triacylglycerols.Keywords
This publication has 19 references indexed in Scilit:
- Postprandial Lipemic Response Is Modified by the Polymorphism at Codon 54 of the Fatty Acid–Binding Protein 2 GeneArteriosclerosis, Thrombosis, and Vascular Biology, 1998
- Role of membrane-associated and cytoplasmic fatty acid-binding proteins in cellular fatty acid metabolismProstaglandins, Leukotrienes & Essential Fatty Acids, 1997
- Codon 54 Polymorphism of the Human Intestinal Fatty Acid Binding Protein 2 Gene Is Associated With Dyslipidemias But Not With Insulin Resistance in Patients With Familial Combined HyperlipidemiaArteriosclerosis, Thrombosis, and Vascular Biology, 1997
- A Polymorphism in the Human Intestinal Fatty Acid Binding Protein Alters Fatty Acid Transport across Caco-2 CellsJournal of Biological Chemistry, 1996
- An amino acid substitution in the human intestinal fatty acid binding protein is associated with increased fatty acid binding, increased fat oxidation, and insulin resistance.Journal of Clinical Investigation, 1995
- Postprandial triacylglycerolaemia—Nutritional implicationsProgress in Lipid Research, 1995
- The Phenomenon of a High Triglyceride Response to an Oral Lipid Load in Healthy Subjects and Its Link to the Metabolic Syndrome aAnnals of the New York Academy of Sciences, 1993
- Structure and functional properties of lipoprotein lipaseBiochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1992
- Lipolysis of polyenoic fatty acid esters of human chylomicrons by lipoprotein lipaseEuropean Journal of Clinical Investigation, 1989
- Dietary polyunsaturated fats of the W-6 and W-3 series reduce postprandial lipoprotein levels. Chronic and acute effects of fat saturation on postprandial lipoprotein metabolism.Journal of Clinical Investigation, 1988