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Pharmacogenetic study of cholesteryl ester transfer protein gene and simvastatin treatment in hypercholesterolaemic subjects
被引:25
作者:
Anagnostopoulou, Katherine
Kolovou, Genovefa
Kostakou, Peggy
Mihas, Constantinos
Mikhailidis, Dimitri
Cokkinos, Dennis V.
机构:
[1] Onassis Cardiac Surg Ctr, Cardiol Dept 1, Athens 17674, Greece
[2] Gen Hosp Kimi, Dept Internal Med, Kimi, Greece
[3] Univ London, Royal Free Hosp, Vasc Dis Prevent Clin, Royal Free & Univ Coll Med Sch, London, England
关键词:
cholesteryl ester transfer protein;
genetic polymorphism;
1405V;
simvastatin;
TaqIB;
D O I:
10.1517/14656566.8.15.2459
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Objective: To examine the effect of the 1405V and TaqIB polymorphisms of cholesteryl ester transfer protein (CETP) on the lipid response after simvastatin treatment in 180 hypercholesterolaemic patients. Methods: Hypercholesterolaemic patients (n = 180) attending the lipid clinic at the Onassis Cardiac Surgery Center were genotyped and their response to simvastatin was evaluated. Results: Sequence variations in the CETP gene influenced the effect of lipid-lowering treatment. Specifically, the I allele of the 1405V polymorphism was associated with a greater reduction in triglyceride (TG; p = 0.04) and a significant increase in high-density lipoprotein cholesterol (HDL-C) levels (p = 0.05) after treatment compared with the V allele. Conclusions: The authors' findings suggest that CETP 1405V polymorphism modifies the effect of simvastatin on TG reduction and HDL-C elevation; the carriers of the I allele responded better to treatment. These findings need to be confirmed in larger studies.
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页码:2459 / 2463
页数:5
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