Calcified Tissue International

, Volume 102, Issue 5, pp 607–618 | Cite as

Osteoporosis in Rheumatic Diseases: Anti-rheumatic Drugs and the Skeleton

  • Alanna M. Dubrovsky
  • Mie Jin Lim
  • Nancy E. Lane
Review

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.

Keywords

Rheumatoid arthritis Ankylosing spondylitis Anti-rheumatic drug Osteoporosis Bone loss Anti-osteoporotic medication 

Notes

Acknowledgements

This work was supported in part by Inha University, Incheon, Korea, endowment for Dr. Nancy E. Lane at UC Davis, NIH Grant P50 AR063043 (NEL).

Compliance with Ethical Standards

Conflict of interest

Alanna M. Dubrovsky, Mie Jin Lim, Nancy E. Lane have no conflicts of interest related to this work.

Human and Animal Rights and Informed Consent

There were no human or animal studies that were performed by the authors that were described in this work.

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Center for Musculoskeletal HealthUniversity of California at Davis Medical CenterSacramentoUSA
  2. 2.Division of Rheumatology, Department of Internal MedicineInha University HospitalIncheonSouth Korea
  3. 3.Department of Internal MedicineUniversity of California at Davis Medical CenterSacramentoUSA

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