Impact of atorvastatin and omega-3 ethyl esters 90 on plasma plant sterol concentrations and cholesterol synthesis in type 2 diabetes: a randomised placebo controlled factorial trial

Atherosclerosis. 2010 Dec;213(2):512-7. doi: 10.1016/j.atherosclerosis.2010.09.013. Epub 2010 Sep 18.

Abstract

Objective: To determine the effects of statin treatment and omega-3 polyunsaturated fatty acid supplementation on plasma plant sterol concentrations and cholesterol synthesis in patients with type 2 diabetes.

Methods: Plant sterol concentrations and lanosterol (a marker of cholesterol synthesis) were measured using a high sensitivity assay to assess the effect of double-blind daily treatment for 4 months with atorvastatin 20mg or placebo and, in a 2 × 2 factorial design, omega-3 ethyl esters 90 2g or placebo.

Results: 658 patients were included in a per protocol analysis. The 4 treatment groups had similar mean [SD] age (63.5 years [11.7]), HbA(1c) (6.9% [1.1]) and diabetes duration (median 4 years [inter-quartile range 2, 8]). Atorvastatin treatment alone reduced low density lipoprotein (LDL) cholesterol by 1.4 mmol/l (44%, p<0.001), triglycerides by 0.3 mmol/l (20%, p<0.0001) and lanosterol by 0.36 μmol/l (72%, p<0.001). There was no significant placebo adjusted change in median [95% confidence intervals] total plant sterol concentrations (-0.77 μmol/l [inter-quartile range -2.13, 0.59]), although they were increased significantly with omega-3-acid EE90 treatment (3.23 μmol/l [1.28, 5.17]). There was a 27% smaller reduction in LDL cholesterol with atorvastatin treatment in low cholesterol synthesisers with high absorption, defined by changes at or above the median lanosterol and campesterol levels, respectively, compared with the obverse group (difference 0.42 mmol/l [0.21, 0.62]).

Conclusion: Treatment with atorvastatin in type 2 diabetes did not change median total plasma plant sterol concentrations, but LDL cholesterol was reduced most efficaciously in high cholesterol synthesisers with low intestinal cholesterol absorption.

Clinical trial registration information: Current controlled trials number ISRCTN: 76737502 (http://isrctn.org).

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anticholesteremic Agents / therapeutic use
  • Atorvastatin
  • Cholesterol / analogs & derivatives
  • Cholesterol / biosynthesis*
  • Cholesterol / blood
  • Cholesterol, LDL / blood
  • Diabetes Mellitus, Type 2 / drug therapy
  • Diabetes Mellitus, Type 2 / metabolism*
  • Docosahexaenoic Acids / therapeutic use*
  • Double-Blind Method
  • Drug Combinations
  • Eicosapentaenoic Acid / therapeutic use*
  • Heptanoic Acids / therapeutic use*
  • Humans
  • Lanosterol / blood
  • Phytosterols / blood
  • Pyrroles / therapeutic use*
  • Triglycerides / blood

Substances

  • Anticholesteremic Agents
  • Cholesterol, LDL
  • Drug Combinations
  • Heptanoic Acids
  • Phytosterols
  • Pyrroles
  • Triglycerides
  • Lanosterol
  • Docosahexaenoic Acids
  • campesterol
  • Cholesterol
  • Atorvastatin
  • Eicosapentaenoic Acid
  • Omacor

Associated data

  • ISRCTN/ISRCTN76737502