(Circulation. 2001;103:792.)
© 2001 American Heart Association, Inc.
Clinical Investigation and Reports |
From the Department of Medicine, University of Washington, Seattle.
Correspondence to John D. Brunzell, MD, University of Washington, Department of Medicine, 1959 NE Pacific St, Box 356426, Seattle, WA 98195-6426. E-mail brunzell{at}u.washington.edu
BackgroundThe
common -514
C
T
polymorphism in the promoter region of the hepatic lipase (HL) gene
affects HL activity. The C
allele is associated with higher HL activity, more dense and
atherogenic LDL, and lower HDL2 cholesterol.
Intensive lipid-lowering therapy lowers HL activity, increases LDL and
HDL buoyancy, and promotes coronary artery disease (CAD) regression. We
tested the hypothesis that subjects with the
CC genotype and a more
atherogenic lipid profile experience the greatest CAD regression from
these favorable effects.
Methods and ResultsForty-nine middle-aged men with dyslipidemia and established CAD who were undergoing intensive lipid-lowering therapy were studied. Change in coronary stenosis was assessed by quantitative angiography, HL polymorphism by polymerase chain reaction amplification, HL activity by 14C-labeled substrate, and LDL buoyancy by density-gradient ultracentrifugation. The response to lipid-lowering therapy was significantly different among subjects with different HL promoter genotypes. Subjects with the CC genotype had the greatest decrease in HL activity (P<0.005 versus TC and TT by ANOVA) and the greatest improvement in LDL density (P<0.005) and HDL2-C (P<0.05) with therapy. These subjects had the greatest angiographic improvement, with 96% of them experiencing CAD regression, compared with 60% of TC and none of the TT patients (P<0.001).
ConclusionsIn
middle-aged men with established CAD and dyslipidemia, the HL gene
-514
C
T
polymorphism significantly predicts changes in coronary stenosis with
lipid-lowering treatment that appear to involve an HL-associated effect
on LDL metabolism. This study identifies a gene polymorphism that
strongly influences the lipid and clinical response to lipid-lowering
drugs.
Key Words: coronary artery disease liver genes lipoproteins pharmacogenetics
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