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A Novel in vivo Gene Transfer Technique and in vitro Cell Based Assays for the Study of Bone Loss in Musculoskeletal Disorders
Published on: June 8, 2014
Anti-resorptive therapies for osteoporosis
1Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand. i.reid@auckland.ac.nz
Abstract:
The treatment of osteoporosis is largely based around the use of agents that inhibit bone resorption by osteoclasts. The main classes of anti-resorptives currently in use are calcium, bisphosphonates, estrogen, selective estrogen receptor modulators (SERMs) and calcitonin. Novel agents in development are: inhibitors of the osteoclast enzyme, cathepsin K; and a monoclonal antibody against receptor activator of NFkappaB-ligand (RANKL), a factor made by osteoblasts which stimulates osteoclast development. Potent anti-resorptive agents decrease numbers of vertebral fractures by about 50%, and non-vertebral fractures by only 25%. Whether the newer agents can improve on this remains to be seen, though it is possible that anabolic agents which increase bone mass more substantially will be needed to achieve greater reductions in all fracture numbers.
Insights
Current osteoporosis treatments focus on inhibiting bone resorption. While effective, newer agents and anabolic therapies may be needed for greater fracture reduction.
Area of Science:
- Bone biology and pharmacology
- Osteoporosis treatment strategies
Background:
- Osteoporosis treatment primarily targets osteoclast-mediated bone resorption.
- Established anti-resorptive therapies include calcium, bisphosphonates, estrogen, SERMs, and calcitonin.
Purpose of the Study:
- To review current and emerging therapeutic agents for osteoporosis.
- To discuss the efficacy of anti-resorptive agents in reducing fracture incidence.
- To explore the potential of novel agents and anabolic therapies.
Main Methods:
- Review of existing literature on osteoporosis treatments.
- Analysis of the mechanisms of action for anti-resorptive agents.
- Evaluation of clinical data on fracture reduction efficacy.
Main Results:
- Potent anti-resorptive agents reduce vertebral fractures by approximately 50% and non-vertebral fractures by 25%.
- Emerging treatments include cathepsin K inhibitors and RANKL inhibitors.
- The potential for improved fracture reduction with newer agents is under investigation.
Conclusions:
- Current anti-resorptive therapies offer moderate fracture protection.
- Novel agents targeting cathepsin K and RANKL are under development.
- Anabolic agents may be necessary for substantial reductions in all fracture types.
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