Atorvastatin Decreases Apolipoprotein C-III in Apolipoprotein B-Containing Lipoprotein and HDL in Type 2 Diabetes

A potential mechanism to lower plasma triglycerides

  1. Geesje M. Dallinga-Thie, PHD1,
  2. Ingrid I.L. Berk-Planken, MD, PHD2,
  3. Aart H. Bootsma, MD, PHD2,
  4. Hans Jansen, PHD234 and
  5. on behalf of the Diabetes Atorvastatin Lipid Intervention (DALI) Study Group*
  1. 1Department of Internal Medicine, University Medical Center Utrecht, Utrecht, the Netherlands
  2. 2Department of Internal Medicine, Erasmus Medical Center, Rotterdam, the Netherlands
  3. 3Department of Biochemistry, Erasmus Medical Center, Rotterdam, the Netherlands
  4. 4Department of Clinical Chemistry, Erasmus Medical Center, Rotterdam, the Netherlands
  1. Address correspondence and reprint requests to Dr. G.M. Dallinga-Thie, Laboratory of Vascular Medicine and Metabolism, Room Bd 277, Department of Internal Medicine, Erasmus MC, Dr Molewaterplein 40, 3015 GD Rotterdam, P.O. Box 2040, 3000CA Rotterdam, Netherlands. E-mail: g.dallinga{at}erasmusmc.nl

Abstract

OBJECTIVE—Apolipoprotein (apo)C-III is a constituent of HDL (HDL apoC-III) and of apoB-containing lipoproteins (LpB:C-III). It slows the clearance of triglyceride-rich lipoproteins (TRLs) by inhibition of the activity of the enzyme lipoprotein lipase (LPL) and by interference with lipoprotein binding to cell-surface receptors. Elevated plasma LpB:C-III is an independent risk factor for cardiovascular disease. We studied the effect of atorvastatin on plasma LpB:C-III and HDL apoC-III.

RESEARCH DESIGN AND METHODS—We studied the effect of 30 weeks’ treatment with 10 and 80 mg atorvastatin on plasma apoC-III levels in a randomized, double-blind, placebo-controlled trial involving 217 patients with type 2 diabetes and fasting plasma triglycerides between 1.5 and 6.0 mmol/l.

RESULTS—Baseline levels of total plasma apoC-III, HDL apoC-III, and LpB:C-III were 41.5 ± 10.0, 17.7 ± 5.5, and 23.8 ± 7.7 mg/l, respectively. Plasma apoC-III was strongly correlated with plasma triglycerides (r = 0.74, P < 0.001). Atorvastatin 10- and 80-mg treatment significantly decreased plasma apoC-III (atorvastatin 10 mg, 21%, and 80 mg, 27%), HDL apoC-III (atorvastatin 10 mg, 22%, and 80 mg, 28%) and LpB:C-III (atorvastatin 10 mg, 23%, and 80 mg, 28%; all P < 0.001). The decrease in plasma apoC-III, mainly in LpB:C-III, strongly correlated with a decrease in triglycerides (atorvastatin 10 mg, r = 0.70, and 80 mg, r = 0.78; P < 0.001). Atorvastatin treatment also leads to a reduction in the HDL apoC-III-to-HDL cholesterol and HDL apoC-III-to-apoA-I ratios, indicating a change in the number of apoC-III per HDL particle (atorvastatin 10 mg, −21%, and 80 mg, −31%; P < 0.001).

CONCLUSIONS—Atorvastatin treatment resulted in a significant dose-dependent reduction in plasma apoC-III, HDL apoC-III, and LpB:C-III levels in patients with type 2 diabetes. These data indicate a potentially important antiatherogenic effect of statin treatment and may explain (part of) the triglyceride-lowering effect of atorvastatin.

Footnotes

  • *An appendix at the end of this article lists the members of the DALI study group.

  • A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.

    • Accepted March 16, 2004.
    • Received October 7, 2003.
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