Response to cholesterol-lowering drugs in familial defective apolipoprotein B-100

Atherosclerosis. 1991 Nov;91(1-2):73-6. doi: 10.1016/0021-9150(91)90188-9.

Abstract

The effect of cholestyramine and simvastatin, given separately or in combination, on serum lipid concentrations in 11 patients with heterozygous familial defective apolipoprotein B-100 was compared with that in 11 matched patients with heterozygous familial hypercholesterolaemia. In both groups of patients there was a substantial fall in serum lipid levels in response to treatment. There were no significant differences between the reductions in serum total or low-density lipoprotein cholesterol levels in the two groups.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Anticholesteremic Agents / therapeutic use*
  • Apolipoprotein B-100
  • Apolipoproteins B / genetics*
  • Apolipoproteins E / genetics
  • Cholesterol / blood
  • Cholesterol, LDL / blood
  • Cholestyramine Resin / therapeutic use
  • Drug Therapy, Combination
  • Female
  • Heterozygote
  • Humans
  • Hypercholesterolemia / blood
  • Hypercholesterolemia / drug therapy*
  • Hypercholesterolemia / genetics
  • Lovastatin / analogs & derivatives
  • Lovastatin / therapeutic use
  • Male
  • Middle Aged
  • Phenotype
  • Simvastatin
  • Triglycerides / blood

Substances

  • Anticholesteremic Agents
  • Apolipoprotein B-100
  • Apolipoproteins B
  • Apolipoproteins E
  • Cholesterol, LDL
  • Triglycerides
  • Cholestyramine Resin
  • Cholesterol
  • Lovastatin
  • Simvastatin