Jamshidi, Y and Flavell, DM and Hawe, E and MacCallum, PK and Meade, TW and Humphries, SE (2002) Genetic determinants of the response to bezafibrate treatment in the lower extremity arterial disease event reduction (LEADER) trial. ATHEROSCLEROSIS , 163 (1) 183 - 192.
Full text not available from this repository.
Genetic determinants of baseline levels and the fall in plasma triglyceride and fibrinogen levels in response to bezafibrate treatment were examined in 853 men taking part in the lower extremity arterial disease event reduction (LEADER) trial. Three polymorphisms in the peroxisome proliferator activated receptor alpha (PPARalpha) gene were investigated (L162V, G > A in intron 2 and G > C in intron 7), two in the apolipoprotein CIII (APOC3) gene (-482C > T and -455T > Q and one in the beta-fibrinogen (FIBB) gene (-455G > A). The presence of diabetes (n = 158) was associated with 15% higher triglyceride levels at baseline compared to non-diabetics (n = 654) (P < 0.05). Among the diabetic group, carriers of the PPAR alpha intron 7 C allele had 20% lower triglyceride levels compared to homozygotes for the common G allele (P <0.05), with a similar (non-significant) trend for the L162V polymorphism, which is in linkage disequilibrium with the intron 7 polymorphism. For the APOC3 gene, carriers of the -482T allele had 13% lower baseline triglyceride levels compared to -482C homozygotes (P < 0.02), but no effect was observed with the 455T > C substitution. In the non-diabetic patients, the PPARalpha V162 allele was significantly associated with 9% higher baseline triglyceride levels (P < 0.03) and a similar, but non-significant trend was seen for the intron 7 polymorphism. Overall, triglyceride levels fell by 26% with 3 months of bezafibrate treatment, and current smokers showed a poorer response compared to ex/non-smokers (23% fall compared to 28% P = 0.03), but none of the genotypes examined had a significant influence on the magnitude of response. Carriers of the -455A polymorphism of the FIBB gene had, as expected, marginally higher baseline fibrinogen levels, 3.43 versus 3.36 g/l (P = 0.055), but this polymorphism did not affect response to treatment. Overall, fibrinogen levels fell by 12%, with patients with the highest baseline fibrinogen levels showing the greatest decrease in response to bezafibrate. For both the intron 2 and the L162V polymorphisms of the PPAR alpha gene there was a significant interaction (both P <0.01) between genotype and baseline levels of fibrinogen on the response of fibrinogen levels to bezafibrate, such that individuals carrying the rare alleles in the lowest fertile showed essentially no overall decrease compared to a 0.18 g/l fall in homozygotes for the common allele. Thus while these genotypes are a minor determinant of baseline triglyceride and fibrinogen levels, there is little evidence from this study that the magnitude of response to bezafibrate treatment in men with peripheral vascular disease is determined by variation at these loci. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
|Title:||Genetic determinants of the response to bezafibrate treatment in the lower extremity arterial disease event reduction (LEADER) trial|
|Keywords:||apolipoprotein CIII, bezafibrate, fibrinogen, gene polymorphism, peroxisome proliferator activated receptor alpha triglycerides, PROLIFERATOR-ACTIVATED RECEPTOR, ISCHEMIC-HEART-DISEASE, APOLIPOPROTEIN-A-I, PPAR-GAMMA ACTIVATORS, INTERMITTENT CLAUDICATION, RISK-FACTORS, FATTY-ACIDS, CARDIOVASCULAR-DISEASE, ATHEROSCLEROSIS RISK, HEMOSTATIC FACTORS|
|UCL classification:||UCL > School of Life and Medical Sciences > Faculty of Population Health Sciences > Institute of Cardiovascular Science|
Archive Staff Only: edit this record