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The Journal of Bone and Joint Surgery (American) 84:236-249 (2002)
© 2002 The Journal of Bone and Joint Surgery, Inc.


Scientific Article

Effects of Alendronate on Particle-Induced Osteolysis in a Rat Model

Peter J. Millett, MDM, MSc, Matthew J. Allen, MA, VetMB, PhD and Mathias P.G. Bostrom, MD

Investigation performed at The Hospital for Special Surgery, New York, and State University of New York, Upstate Medical University, Syracuse, NY

Peter J. Millett, MD, MSc
Department of Orthopaedics, Harvard Medical School, Brigham and Women’s Hospital, 75 Francis Street, Boston, MA 02115

Matthew J. Allen, MA, VetMB, PhD
Department of Orthopaedic Surgery, State University of New York, Upstate Medical University, 750 East Adams Street, Syracuse, NY 13210

Mathias P.G. Bostrom, MD
The Hospital for Special Surgery, 535 East 70th Street, New York, NY 10021

No benefits in any form have been received or will be received from a commercial party related directly or indirectly to the subject of this article. Funds were received in total or partial support of the research or clinical study presented in this article. The funding source was the Orthopaedic Research and Education Foundation Resident Research Award.Recipient of the American Orthopaedic Assocation-Zimmer Resident Travel Award and the Lewis Clark Wagner Award for Excellence in Orthopaedic Research, The Hospital for Special Surgery

Background: Particle-induced osteolysis is currently a major problem affecting the long-term survivorship of total joint replacements. Alendronate is a third-generation bisphosphonate that blocks osteoclastic bone resorption. The objective of this study was to determine whether alendronate could prevent particle-induced osteolysis or restore (reverse) bone loss in established osteolysis.

Methods: A rat model of particle-induced osteolysis was used. A specially designed polyethylene implant was placed in the proximal part of the right tibia of seventy-two animals. Following four weeks of healing, the animals were randomized into control groups, a prevention group, or a treatment group. In the prevention group, animals received intra-articular injections of high-density polyethylene particles (mean size, 2 m; all <10 m) at four, six, and eight weeks postoperatively. Alendronate (0.01 mg/kg/day) was administered concomitantly through an implantable pump from the fourth week through the tenth week. In the treatment group, animals were also exposed to polyethylene particles at four, six, and eight weeks, to establish bone loss, but they received alendronate subsequently, from the tenth week through the sixteenth week, to treat the bone loss. Positive (particle-only) and negative (saline-solution-only) control groups were assessed as well. Tissues were harvested at ten weeks in the prevention group and at sixteen weeks in the treatment group. Histological analyses and histomorphometric determinations of the periprosthetic bone volume were carried out.

Results: Histological examination showed a rim of new bone (neocortex) around the implant in the untreated and saline-solution-treated control animals (no polyethylene particles). Treatment with saline solution (no polyethylene particles) did not affect periprosthetic bone. Animals exposed to polyethylene particles had bone loss. In those that received alendronate, the bone loss was either prevented or reversed, and the quantity of neocortical and trabecular bone was increased compared with that of the controls. Alendronate effectively preserved periprosthetic bone in both the prevention and treatment groups.

In the prevention arm, the mean periprosthetic bone volume of the neocortex and the surrounding trabecular bone, as determined with histomorphometry, was 21.5% %plusmn; 6.5% in the saline-solution-treated controls (no particles), 13.1% %plusmn; 5.9% in the particle-treated animals, and 32.6% %plusmn; 6.4% in the alendronate-treated animals (p < 0.001). In the treatment arm, the mean periprosthetic bone volume was 27.2% %plusmn; 5.6% in the saline-solution-treated controls, 17.7% %plusmn; 6.2% in the particle-treated animals, and 30.2% %plusmn; 5.9% in the alendronate-treated animals (p = 0.002).

Conclusions: In our model, the intra-articular injection of polyethylene particles caused substantial bone loss around a loaded implant. Alendronate effectively prevented and treated the particle-induced periprosthetic bone loss.

Clinical Relevance: Alendronate may be useful in preventing particle-induced osteolysis around total joint implants. It may also elicit bone formation in established osteolytic lesions.


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