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Clinical Trial
. 2007 Jun;27(6):1417-25.
doi: 10.1161/ATVBAHA.107.140103. Epub 2007 Apr 12.

Fenofibrate effect on triglyceride and postprandial response of apolipoprotein A5 variants: the GOLDN study

Affiliations
Clinical Trial

Fenofibrate effect on triglyceride and postprandial response of apolipoprotein A5 variants: the GOLDN study

Chao-Qiang Lai et al. Arterioscler Thromb Vasc Biol. 2007 Jun.

Abstract

Objective: Apolipoprotein A5 (APOA5) is a key determinant of plasma triglyceride (TG) concentrations. Genetic variation at the APOA5 locus could be responsible for some of the observed differences in response to fenofibrate therapy.

Methods and results: We examined the association between tag SNPs (-1131T>C and 56C>G) at APOA5 and TG and HDL-C response to fenofibrate and a postprandial lipid challenge in 791 men and women participating in the GOLDN study. After 3-week drug treatment, APOA5 56G carriers displayed significant decrease in TG (P=0.006), and increase in HDL-C (P=0.002) levels relative to their basal values in the fasting state when compared with noncarriers (a TG reduction of -35.8+/-2.8% versus -27.9+/-0.9% and a HDL-C increase of 11.8+/-1.3% versus 6.9+/-0.5%, respectively). In the postprandial lipemia after a fat load, the 56G carriers showed a significant decrease in the area under curve for TG and increase for HDL-C than the noncarriers. These diverse beneficial responses of 56G carriers to fenofibrate were further characterized by a higher increase in large LDL-C concentrations and LDL size. On the other hand, subjects with different APOA5-1131T>C genotypes showed no significant response to fenofibrate intervention.

Conclusion: This study suggests that the APOA5 56G carriers benefited more from the fenofibrate treatment than noncarriers in lowering plasma TG and increasing HDL-C levels.

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