Zoledronic acid protects against local and systemic bone loss in tumor necrosis factor–mediated arthritis

• Published in: Arthritis and rheumatism 2004-07, Vol.50 (7), p.2327-2337
• Main Authors: Herrak, Petra, Görtz, Birgit, Hayer, Silvia, Redlich, Kurt, Reiter, Erika, Gasser, Jürg, Bergmeister, Helga, Kollias, Giorgos, Smolen, Josef S., Schett, Georg
• Format: Article
• Language: English
• Subjects: Animals; Antibodies, Monoclonal - pharmacology; Arthritis - complications; Arthritis - diagnosis; Arthritis - etiology; Arthritis - physiopathology; Arthrography; Biological and medical sciences; Bone and Bones - diagnostic imaging; Bone and Bones - drug effects; Bone and Bones - pathology; Bone Density - drug effects; Bone Resorption - etiology; Bone Resorption - pathology; Bone Resorption - prevention & control; Calcitonin - pharmacology; Cartilage, Articular - drug effects; Cartilage, Articular - pathology; Diphosphonates - pharmacology; Diseases of the osteoarticular system; Hindlimb; Humans; Imidazoles - pharmacology; Infliximab; Joints - drug effects; Joints - pathology; Medical sciences; Mice; Mice, Transgenic; Miscellaneous. Osteoarticular involvement in other diseases; Osteoclasts - drug effects; Osteoclasts - pathology; Osteogenesis - drug effects; Tomography, X-Ray Computed; Tumor Necrosis Factor-alpha - metabolism
• ISSN: 0004-3591; 1529-0131
• DOI: 10.1002/art.20384

Objective Increased osteoclast activity is a key factor in bone loss in rheumatoid arthritis (RA). This suggests that osteoclast‐targeted therapies could effectively prevent skeletal damage in patients with RA. Zoledronic acid (ZA) is one of the most potent agents for blocking osteoclast function. We therefore investigated whether ZA can inhibit the bone loss associated with chronic inflammatory conditions. Methods Human tumor necrosis factor (TNF)–transgenic (hTNFtg) mice, which develop severe destructive arthritis as well as osteoporosis, were treated with phosphate buffered saline, single or repeated doses of ZA, calcitonin, or anti‐TNF, at the onset of arthritis. Results Synovial inflammation was not affected by ZA. In contrast, bone erosion was retarded by a single dose of ZA (−60%) and was almost completely blocked by repeated administration of ZA (−95%). Cartilage damage was partly inhibited, and synovial osteoclast counts were significantly reduced with ZA treatment. Systemic bone mass dramatically increased in hTNFtg mice after administration of ZA, which was attributable to an increase in trabecular number and connectivity. In addition, bone resorption parameters were significantly lowered after administration of ZA. Calcitonin had no effect on synovial inflammation, bone erosion, cartilage damage, or systemic bone mass. Anti‐TNF entirely blocked synovial inflammation, bone erosion, synovial osteoclast formation, and cartilage damage but had only minor effects on systemic bone mass. Conclusion ZA appears to be an effective tool for protecting bone from arthritic damage. In addition to their role in antiinflammatory drug therapy, modern bisphosphonates are promising candidates for maintaining joint integrity and reversing systemic bone loss in patients with arthritis.