American Journal of Cardiology
Volume 102, Issue 11 , Pages 1495-1501, 1 December 2008

Efficacy and Safety of Ezetimibe Added on to Atorvastatin (40 mg) Compared With Uptitration of Atorvastatin (to 80 mg) in Hypercholesterolemic Patients at High Risk of Coronary Heart Disease

  • Lawrence A. Leiter, MD

      Affiliations

    • St. Michael's Hospital and University of Toronto, Toronto, Ontario, Canada
    • Corresponding Author InformationCorresponding author: Tel: 416-867-7441; fax: 416-867-3696
  • ,
  • Harold Bays, MD

      Affiliations

    • Louisville Metabolic and Atherosclerosis Research Center, Louisville, Kentucky
  • ,
  • Scott Conard, MD

      Affiliations

    • University of Texas Southwestern Medical School, Dallas, Texas
  • ,
  • Steven Bird, MS

      Affiliations

    • Merck & Co., Inc., North Wales, Pennsylvania
  • ,
  • Joseph Rubino, MBA

      Affiliations

    • Merck & Co., Inc., North Wales, Pennsylvania
  • ,
  • Mary E. Hanson, PhD

      Affiliations

    • Merck & Co., Inc., North Wales, Pennsylvania
  • ,
  • Joanne E. Tomassini, PhD

      Affiliations

    • Merck & Co., Inc., North Wales, Pennsylvania
  • ,
  • Andrew M. Tershakovec, MD

      Affiliations

    • Merck & Co., Inc., North Wales, Pennsylvania

Received 9 September 2008; received in revised form 29 September 2008; accepted 29 September 2008. published online 27 October 2008.

The percentage of change from baseline in low-density lipoprotein (LDL) cholesterol after the addition of ezetimibe 10 mg to atorvastatin 40 mg was compared with uptitration to atorvastatin 80 mg. In this multicenter, double-blind, parallel-group study, adult hypercholesterolemic patients using atorvastatin 40 mg/day were randomly assigned to atorvastatin 40 mg plus ezetimibe 10 mg or uptitration to atorvastatin 80 mg. After 6 weeks of treatment, compared with atorvastatin 80 mg, atorvastatin 40 mg plus ezetimibe significantly reduced the primary end point of LDL cholesterol by −27% versus atorvastatin 80 mg by −11% (p <0.001), as well as significantly reduced non–high-density lipoprotein cholesterol, apolipoprotein B, total cholesterol, and triglycerides significantly more than atorvastatin 80 mg (all p <0.001). Percentages of change in high-sensitivity C-reactive protein, high-density lipoprotein cholesterol, and apolipoprotein A-I were similar between groups. Significantly more patients treated with atorvastatin 40 mg plus ezetimibe reached LDL cholesterol <70 mg/dl versus patients treated with atorvastatin 80 mg (74% vs 32%; p <0.001). Safety and tolerability profiles and incidence of liver and muscle adverse experiences were generally similar between groups. In conclusion, these results showed that adding ezetimibe to atorvastatin 40 mg was significantly more effective than uptitrating to atorvastatin 80 mg at lowering LDL cholesterol and other lipid parameters. Both treatments were generally well tolerated (clinical trial no. NCT00276484).

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 This work was supported by Merck/Schering-Plough Pharmaceuticals, North Wales, Pennsylvania.

PII: S0002-9149(08)01670-6

doi:10.1016/j.amjcard.2008.09.076

American Journal of Cardiology
Volume 102, Issue 11 , Pages 1495-1501, 1 December 2008