American Journal of Cardiology
Volume 105, Issue 5 , Pages 656-663, 1 March 2010

Safety and Efficacy of Ezetimibe Added to Atorvastatin Versus Up Titration of Atorvastatin to 40 mg in Patients ≥65 Years of Age (from the ZETia in the ELDerly [ZETELD] Study)

  • Franklin Zieve, MD, PhD

      Affiliations

    • McGuire Veterans Affairs Medical Center, Richmond, Virginia
    • Corresponding Author InformationCorresponding author: Tel: (804) 675-5151; fax: (804) 675-5139
  • ,
  • Nanette K. Wenger, MD

      Affiliations

    • Emory University School of Medicine, Atlanta, Georgia
  • ,
  • Ori Ben-Yehuda, MD

      Affiliations

    • University of California San Diego Medical Center, San Diego, California
  • ,
  • Christian Constance, MD

      Affiliations

    • Hopital Maisonneuve-Rosemont Recherche Clinique/Polyclinique, Montreal, Quebec, Canada
  • ,
  • Steven Bird, MS

      Affiliations

    • Merck & Company, Inc., North Wales, Pennsylvania
  • ,
  • Raymond Lee, BS

      Affiliations

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

      Affiliations

    • Merck & Company, Inc., North Wales, Pennsylvania
  • ,
  • Charlotte Jones-Burton, MD, MS

      Affiliations

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

      Affiliations

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

Received 3 August 2009; received in revised form 18 October 2009; accepted 18 October 2009. published online 25 December 2009.

Few clinical studies have focused on the efficacy of lipid-lowering therapies in patients ≥65 years of age. The percentage of change from baseline in low-density lipoprotein (LDL) cholesterol and the percentage of patients achieving prespecified LDL cholesterol levels after 12 weeks of ezetimibe 10 mg plus atorvastatin versus up titration of atorvastatin were assessed in subjects ≥65 years old with hyperlipidemia and at high risk of coronary heart disease. After stabilization of atorvastatin 10-mg therapy, 1,053 patients, ≥65 years old, at high risk of coronary heart disease, with and without atherosclerotic vascular disease and a LDL cholesterol level that was not <70 or <100 mg/dl, respectively, were randomized to receive ezetimibe added to atorvastatin 10 mg for 12 weeks versus up titration to atorvastatin 20 mg for 6 weeks followed by up titration to atorvastatin 40 mg for an additional 6 weeks. Ezetimibe added to atorvastatin 10 mg resulted in significantly greater changes at week 6 in LDL cholesterol (p <0.001), significantly more patients with atherosclerotic vascular disease achieving a LDL cholesterol level of <70 mg/dl (p <0.001), and significantly more patients without atherosclerotic vascular disease achieving a LDL cholesterol level of <100 mg/dl (p <0.001) at weeks 6 and 12 compared to atorvastatin 20 mg or atorvastatin 40 mg. In addition, ezetimibe plus atorvastatin 10 mg resulted in significantly greater changes at week 6 in total cholesterol, triglycerides, non–high-density lipoprotein (HDL) cholesterol, apolipoprotein B (all p <0.001), and HDL cholesterol (p = 0.021) compared with atorvastatin 20 mg and significantly greater changes at week 12 in LDL cholesterol, non-HDL cholesterol, apolipoprotein A-I (p = 0.001), total cholesterol, apolipoprotein B (p <0.030), and HDL cholesterol (p <0.001) compared with atorvastatin 40 mg. Both treatments were generally well tolerated, with comparable safety profiles. In conclusion, adding ezetimibe to atorvastatin 10 mg produced significantly greater favorable changes in most lipids at 6 and 12 weeks and significantly greater attainment of prespecified LDL cholesterol levels than doubling or quadrupling the atorvastatin dose in patients ≥65 years old at high risk for coronary heart disease.

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 Dr. Zieve has received research grants from Amylin Pharmaceuticals, Inc., San Diego, California, Abbott Laboratories, Abbot Park, Illinois, GlaxoSmithKline, London, England, Roche, Basel, Switzerland, Novo-Nordisk, Bagsvaerd, Denmark, Merck & Company, Inc., North Wales, Pennsylvania, and Novartis, Basel, Switzerland; has served on the Speaker's Bureau for Merck & Company, Inc., Abbott Laboratories, and GlaxoSmithKline; and holds stock in Johnson & Johnson, Langhorne, Pennsylvania. Dr. Wenger has received research grants or contracts or has been on the trial steering committee or trial adjudication committee for Pfizer, New York, New York, Merck & Company, Inc., North Wales, Pennsylvania, National Heart, Lung, and Blood Institute, Bethesda, Maryland, CV Therapeutics, Palo Alto, California, Abbott Laboratories, Abbott Park, Illinois, Sanofi-Aventis, Bridgewater, New Jersey, Eli Lilly, Indianapolis, Indiana and has acted as a consultant or advisor for Schering-Plough, Kenilworth, New Jersey; AstraZeneca, Wilmington, Delaware; Abbott Laboratories, Abbott Park, Illinois; Merck & Company, Inc., North Wales, Pennsylvania; Pfizer, New York, New York; Boston Scientific, Boston, Massachusetts; and Medtronic, Minneapolis, Minnesota. Dr. Constance has served on the Speaker's Bureau for Merck & Company, Inc., North Wales, Pennsylvania. Dr. Ben-Yehuda has received research grants from Merck & Company, Inc., North Wales, Pennsylvania, and Merck/Schering-Plough, North Wales, Pennsylvania, has served on the Speaker's Bureau for Schering-Plough, Kenilworth, New Jersey, and has acted as a consultant for CV Therapeutics, Palo Alto, California, and Merck & Company, Inc., Drs. Bird, Lee, Hanson, Jones-Burton, and Tershakovec are employees of Merck & Company, Inc., North Wales, Pennsylvania, and might own stock and/or hold stock options in the company.

 All authors were involved in at least one of the following: conception, design, acquisition, analysis, statistical analysis, interpretation of data, drafting the manuscript, and/or revising the manuscript for important intellectual content. All authors provided final approval of the version to be published.

PII: S0002-9149(09)02552-1

doi:10.1016/j.amjcard.2009.10.029

American Journal of Cardiology
Volume 105, Issue 5 , Pages 656-663, 1 March 2010