LACK OF INTERACTION OF APOLIPOPROTEIN-E PHENOTYPE WITH THE LIPOPROTEIN RESPONSE TO LOVASTATIN OR GEMFIBROZIL IN PATIENTS WITH PRIMARY HYPERCHOLESTEROLEMIA
C. Sanllehy et al., LACK OF INTERACTION OF APOLIPOPROTEIN-E PHENOTYPE WITH THE LIPOPROTEIN RESPONSE TO LOVASTATIN OR GEMFIBROZIL IN PATIENTS WITH PRIMARY HYPERCHOLESTEROLEMIA, Metabolism, clinical and experimental, 47(5), 1998, pp. 560-565
The magnitude of serum lipid changes in response to hypolipidemic drug
s varies considerably between individuals. These differences may be du
e to interactions between genetic and environmental factors that effec
t drug bioavailability or the capacity of the lipid-regulating enzyme
and receptor targets to be affected. The apolipoprotein E (apoE) gene
locus has been examined in this regard, but reports are conflicting on
the effect of its variability on the response to hypolipidemic drugs.
We investigated the effect of apoE polymorphism on the serum lipid re
sponse to the hepatic hydroxymethyl glutaryl coenzyme A [HMG CoA) redu
ctase inhibitor lovastatin and the fibric acid derivative gemfibrozil.
Lipoprotein changes were assessed after 12 weeks of therapy in 106 pa
tients with primary hypercholesterolemia and combined hyperlipidemia t
reated with lovastastin and in 63 given gemfibrozil therapy. No signif
icant effect of the apoE phenotypes E3/2, E3/3, or E4/3 on the heterog
eneity of lipid responses to either drug was found. Copyright (C) 1998
by W.B. Saunders Company.