Abstract
We compared the effects of cholesterol-lowering therapy on 2 patient groups genetically defined as heterozygous for familial hypercholesterolemia (FH), 5 with a deletion of exon 15 (FH(Tonami-1)), and 7 with a point mutation at codon 664 (FH(Kanazawa-2)). There were significant differences in both serum and low-density lipoprotein cholesterol reductions between the 2 groups after combination therapy with pravastatin and cholestyramine, and the overall effect of genotype on serial changes in both was significant.
Publication types
-
Comparative Study
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Adult
-
Aged
-
Anion Exchange Resins / therapeutic use*
-
Anticholesteremic Agents / therapeutic use*
-
Bile / metabolism
-
Cholestyramine Resin / therapeutic use*
-
Drug Therapy, Combination
-
Female
-
Genotype
-
Humans
-
Hydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use*
-
Hyperlipoproteinemia Type II / drug therapy*
-
Hyperlipoproteinemia Type II / genetics*
-
Male
-
Middle Aged
-
Pravastatin / therapeutic use*
-
Receptors, LDL / genetics*
-
Treatment Outcome
Substances
-
Anion Exchange Resins
-
Anticholesteremic Agents
-
Hydroxymethylglutaryl-CoA Reductase Inhibitors
-
Receptors, LDL
-
Cholestyramine Resin
-
Pravastatin