No important influence of limited steroid exposure on bone mass during the first year after renal transplantation: a prospective, randomized, multicenter study

Transplantation. 2004 Jul 15;78(1):101-6. doi: 10.1097/01.tp.0000133513.29923.44.

Abstract

Background: Steroid-related bone loss is a recognized complication after renal transplantation. In a prospective, randomized, multicenter study we compared the influence of a steroid-free immunosuppressive regimen with a regimen with limited steroid exposure on the changes in bone mass after renal transplantation.

Methods: A total of 364 recipients of a renal transplant were randomized to receive either daclizumab (1 mg/kg on days 0 and 10 after transplantation; steroid-free group n=186) or prednisone (0.3 mg/kg per day tapered to 0 mg at week 16 after transplantation; steroids group n=178). All patients received tacrolimus, mycophenolate mofetil, and, during the first 3 days, 100 mg prednisolone intravenously. Changes in bone mineral density (BMD) were evaluated in 135 and 126 patients in the steroid-free and steroids group, respectively.

Results: The mean (+/- SD) BMD of the lumbar spine decreased slightly in both groups during the first 3 months after transplantation (steroid-free -1.3 +/- 4.0% [P<0.01]; steroids -2.3 +/-4.2% [P<0.01]). In the following months, lumbar BMD recovered in both groups (P<0.01), resulting in a lumbar BMD at 12 months after transplantation comparable with the baseline value. No difference between the groups was found at 3 months (steroid-free versus steroids +1.0%; 95% confidence interval -0.0%-+2.0%, P=0.060) and at 12 months after transplantation (steroid-free versus steroids +0.9%; 95% confidence interval -0.8%-+2.6%, NS).

Conclusion: The use of a moderate dose of steroids during 4 months after transplantation has no important influence on bone mass during the first year after renal transplantation. On average, both regimens prevented accelerated bone loss.

Publication types

  • Clinical Trial
  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Adult
  • Aged
  • Antibodies, Monoclonal / administration & dosage
  • Antibodies, Monoclonal, Humanized
  • Bone Density / drug effects*
  • Calcium / blood
  • Creatinine / metabolism
  • Daclizumab
  • Female
  • Femoral Neck Fractures / etiology
  • Femoral Neck Fractures / prevention & control
  • Glucocorticoids / administration & dosage*
  • Graft Rejection / drug therapy*
  • Humans
  • Immunoglobulin G / administration & dosage
  • Immunosuppressive Agents / administration & dosage
  • Kidney / physiology
  • Kidney Transplantation*
  • Male
  • Middle Aged
  • Phosphorus / blood
  • Postoperative Complications / etiology
  • Postoperative Complications / prevention & control
  • Prednisone / administration & dosage*
  • Prospective Studies

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Glucocorticoids
  • Immunoglobulin G
  • Immunosuppressive Agents
  • Phosphorus
  • Creatinine
  • Daclizumab
  • Calcium
  • Prednisone