Osteoporosis in Rheumatic Diseases: Anti-rheumatic Drugs and the Skeleton
Alanna M Dubrovsky1, Mie Jin Lim1,2, Nancy E Lane3,4
1Center for Musculoskeletal Health, University of California at Davis Medical Center, Sacramento, CA, 95817, USA.
Abstract:
Osteoporosis in rheumatic diseases is a very well-known complication. Systemic inflammation results in both generalized and localized bone loss and erosions. Recently, increased knowledge of inflammatory process in rheumatic diseases has resulted in the development of potent inhibitors of the cytokines, the biologic DMARDs. These treatments reduce systemic inflammation and have some effect on the generalized and localized bone loss. Progression of bone erosion was slowed by TNF, IL-6 and IL-1 inhibitors, a JAK inhibitor, a CTLA4 agonist, and rituximab. Effects on bone mineral density varied between the biological DMARDs. Medications that are approved for the treatment of osteoporosis have been evaluated to prevent bone loss in rheumatic disease patients, including denosumab, cathepsin K, bisphosphonates, anti-sclerostin antibodies and parathyroid hormone (hPTH 1-34), and have some efficacy in both the prevention of systemic bone loss and reducing localized bone erosions. This article reviews the effects of biologic DMARDs on bone mass and erosions in patients with rheumatic diseases and trials of anti-osteoporotic medications in animal models and patients with rheumatic diseases.
Insights
Biologic disease-modifying antirheumatic drugs (DMARDs) slow bone erosion in rheumatic diseases by reducing inflammation. Osteoporosis medications also show efficacy in preventing bone loss and reducing erosions in these patients.
Area of Science:
- Rheumatology
- Bone Metabolism
- Immunology
Background:
- Rheumatic diseases frequently cause osteoporosis, characterized by generalized and localized bone loss due to systemic inflammation.
- Biologic disease-modifying antirheumatic drugs (DMARDs) target inflammatory cytokines, offering potential benefits for bone health in rheumatic conditions.
Purpose of the Study:
- To review the impact of biologic DMARDs on bone mass and erosions in patients with rheumatic diseases.
- To evaluate the efficacy of anti-osteoporotic medications in preventing bone loss and reducing erosions in rheumatic disease models and patients.
Main Methods:
- Review of existing literature on biologic DMARDs (TNF, IL-6, IL-1 inhibitors, JAK inhibitors, CTLA4 agonists, rituximab) and their effects on bone.
- Analysis of studies on osteoporosis treatments (denosumab, cathepsin K inhibitors, bisphosphonates, anti-sclerostin antibodies, hPTH 1-34) in rheumatic disease contexts.
Main Results:
- Biologic DMARDs demonstrated a slowing effect on bone erosion progression.
- Effects of biologic DMARDs on bone mineral density varied.
- Anti-osteoporotic medications showed efficacy in preventing systemic bone loss and reducing localized bone erosions.
Conclusions:
- Biologic DMARDs can mitigate bone loss and erosions in rheumatic diseases by controlling inflammation.
- Established osteoporosis therapies hold promise for managing bone complications in patients with rheumatic diseases.
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