Effects of the FABP2 A54T mutation on triglyceride metabolism of viscerally obese men

Citation
Mt. Berthier et al., Effects of the FABP2 A54T mutation on triglyceride metabolism of viscerally obese men, OBES RES, 9(11), 2001, pp. 668-675
Citations number
39
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
OBESITY RESEARCH
ISSN journal
10717323 → ACNP
Volume
9
Issue
11
Year of publication
2001
Pages
668 - 675
Database
ISI
SICI code
1071-7323(200111)9:11<668:EOTFAM>2.0.ZU;2-7
Abstract
Objective: Viscerally obese individuals are frequently characterized by a p roatherogenic condition. A missense mutation (A54T) in the fatty acid bindi ng protein type 2 (FABP2) gene has been associated with insulin resistance and obesity. This study examined the effect of this mutation on lipoprotein levels in viscerally obese hyperinsulinemic condition. Research Methods and Procedures: A total of 217 men were assigned to one of two groups based on their FABP2 A54T polymorphism. Results: The two genotypic groups showed no difference in either physiologi cal characteristics or lipoprotein/lipid profile, before or after statistic al adjustment for age. From this initial sample, 50 men accepted to have th eir postprandial lipid response assessed and 10 T54/A54 heterozygotes were then individually matched for visceral adipose tissue accumulation and fast ing plasma triglyceride (TG) levels with 10 A54/A54 homozygotes. high-densi ty lipoprotein (HDL)TG levels were significantly increased in the fasting s tate as well as 4 hours after the test meal (p = 0.04 and p = 0.0008, respe ctively) in men bearing the A54T mutation. In addition, the area under the curve of postprandial HDL-TG levels was also significantly higher among T54 /A54 heterozygotes than among A54/A54 homozygotes (p = 0.04). Interestingly , fasting TG concentrations in large TG-rich lipoproteins (large-TRL; S-f > 400) were correlated with HDL-TG levels at 4 (r = 0.74, p = 0.01) and 8 ho urs (r = 0.73, p = 0.01) after the test meal in T54/A54 heterozygotes only. Discussion: The FABP2 A54T missense mutation may contribute to the TG enric hment of HDL in the postprandial state that, in turn, may alter the risk of atherosclerotic vascular disease.