American Heart Journal
Volume 149, Issue 5 , Pages 820-825, May 2005

Potential antiatherogenic and anti-inflammatory properties of sevelamer in maintenance hemodialysis patients

  • Emiliana Ferramosca, MD

      Affiliations

    • Section of Cardiology, Department of Medicine, Tulane University School of Medicine, New Orleans, La
  • ,
  • Steven Burke, MD

      Affiliations

    • Drug Discovery and Development, Genzyme Therapeutics, Waltham, Mass
  • ,
  • Scott Chasan-Taber, PhD

      Affiliations

    • Pioneer BioDiligence, Amherst, Mass
  • ,
  • Carlo Ratti, MD

      Affiliations

    • Section of Cardiology, Department of Medicine, Tulane University School of Medicine, New Orleans, La
  • ,
  • Glenn M. Chertow

      Affiliations

    • Division of Nephrology, Department of Medicine, University of California, San Francisco, San Francisco, Calif
  • ,
  • Paolo Raggi, MD

      Affiliations

    • Section of Cardiology, Department of Medicine, Tulane University School of Medicine, New Orleans, La
    • Corresponding Author InformationReprint requests: Paolo Raggi, MD, Tulane University School of Medicine, 1430 Tulane Avenue, SL48, New Orleans, LA 70112.

Received 19 April 2004; accepted 27 July 2004.

Background

Patients affected by end-stage renal disease (ESRD) demonstrate a very high cardiovascular risk mediated by traditional cardiovascular risk factors as well as abnormal mineral metabolism and a state of chronic inflammation. Sevelamer is a nonabsorbable non–calcium-based hydrogel with potential antiatherosclerotic properties.

Method and Results

One hundred eight patients undergoing maintenance hemodialysis were randomized to sevelamer or calcium acetate as treatment for hyperphosphatemia. A coronary artery calcium score, as a measure of plaque burden, was calculated at baseline and 1 year, along with serial measurements of serum lipoproteins, β2-microglobulin, and high-sensitivity C-reactive protein (hs-CRP). At 1 year, coronary artery calcium score progressed significantly from baseline in calcium acetate–treated subjects (P < .001) but not in sevelamer-treated patients (P = NS). Total cholesterol (P < .0001), low-density lipoprotein cholesterol (P < .0001), apolipoprotein B (P < .0001), β2-microglobulin (P = .018), and hs-CRP (P < .002) decreased, and high-density lipoprotein increased significantly (P = .036) from baseline in the sevelamer-treated subjects but not in subjects treated with calcium acetate despite the more frequent use of statins in the latter group (46% vs 22%, P < .05). The changes in total and low-density lipoprotein cholesterol, apolipoprotein B, and hs-CRP were significantly different between treatment groups (all P < .01).

Conclusions

Sevelamer leads to favorable changes in lipids and inflammatory markers with potentially useful antiatherogenic effects in hemodialysis patients.

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PII: S0002-8703(04)00459-4

doi:10.1016/j.ahj.2004.07.023

American Heart Journal
Volume 149, Issue 5 , Pages 820-825, May 2005