Effect of atorvastatin treatment on lipoprotein lipase mass in the pre-heparin plasma in Japanese hyperlipidemic subjects

Clin Chim Acta. 2001 Dec;314(1-2):261-4. doi: 10.1016/s0009-8981(01)00701-x.

Abstract

Background: Atorvastatin is a recently introduced statin that lowers LDL-cholesterol (LDL-C) and triglycerides more than some of the older statins.

Methods: Twenty-one Japanese hyperlipidemic subjects were treated with atorvastatin (10 mg/day) for 6 weeks. Plasma lipid concentrations and pre-heparin plasma LPL mass before and after oral administration were evaluated using an open crossover trial format. LPL mass in the pre-heparin plasma was measured by a sandwich enzyme immunoassay.

Results: Atorvastatin decreased plasma triglyceride (TG) concentration (-21%, p<0.05), as well as plasma total and LDL-cholesterol concentrations. LPL mass in the pre-heparin plasma did not change significantly by this treatment during this period. Both apolipoprotein (apo) B and E decreased considerably (-33%, p<0.001 for apo B; -29% p<0.001 for apo E), while apo A-I concentration did not change. Other clinical parameters such as body mass index, blood pressure, and fasting plasma glucose concentration of these subjects did not change during this treatment.

Conclusions: Atorvastatin is effective in reducing plasma TG, which did not appear to be associated with an increased LPL mass.

Publication types

  • Clinical Trial

MeSH terms

  • Aged
  • Apolipoproteins B / metabolism
  • Apolipoproteins E / metabolism
  • Atorvastatin
  • Blood Glucose / metabolism
  • Cross-Over Studies
  • Female
  • Heptanoic Acids / therapeutic use*
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use*
  • Hyperlipidemias / drug therapy*
  • Hyperlipidemias / enzymology*
  • Lipoprotein Lipase / blood*
  • Male
  • Middle Aged
  • Pyrroles / therapeutic use*
  • Triglycerides / blood

Substances

  • Apolipoproteins B
  • Apolipoproteins E
  • Blood Glucose
  • Heptanoic Acids
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Pyrroles
  • Triglycerides
  • Atorvastatin
  • Lipoprotein Lipase