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.