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The Effect of LDL-cholesterol and Treatment with Losartan on End-stage Renal Disease in the RENAAL Study

  1. Andrew M. Tershakovec, MD (andrew_tershakovec{at}merck.com)1,
  2. William F. Keane, MD1,
  3. Zhongxin Zhang, PhD1,
  4. Paulette A. Lyle, BS1,
  5. Gerald B. Appel, MD2,
  6. Janet B. McGill, MD3,
  7. Hans-Henrik Parving, MD4,
  8. Mark E. Cooper, MD, PhD5,
  9. Shahnaz Shahinfar, MD1 and
  10. Barry M. Brenner, MD6
  1. 1Merck & Co., Inc., Upper Gwynedd, PA
  2. 2Columbia University, New York, NY
  3. 3Washington University, St. Louis, MO
  4. 4University Hospital of Copenhagen, Copenhagen, Denmark
  5. 5Baker Heart Research Institute, Melbourne, Australia
  6. 6Renal Division, Brigham and Women's Hospital, Boston, MA

    Abstract

    Abstract Renal pathology and dyslipidemia commonly coexist. Treatments that lower albuminuria/proteinuria may lower lipids but it is not known whether lipid lowering independent of lessening albuminuria/proteinuria slows progression of kidney disease. We examined the association between low-density lipoprotein cholesterol (LDL-C) levels and treatment with losartan on end-stage renal disease (ESRD). Lipid levels and albuminuria measurements were obtained at baseline and at Year 1 in a post hoc analysis from the Reduction of Endpoints in NIDDM with the Angiotensin II Antagonist Losartan (RENAAL) study, which compared the effects of losartan- versus placebo-based antihypertensive therapy in patients with type 2 diabetes and nephropathy. LDL-C lowering was associated with a lower risk of ESRD; however, this seemed to be largely an association with the reduction in albuminuria.

    Footnotes

      • Received January 31, 2007.
      • Accepted December 4, 2007.

    This Article

    1. Diabetes Care December 10, 2007
    1. All Versions of this Article:
      1. dc07-0196v1
      2. 31/3/445 most recent
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