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Infection and medication-related osteonecrosis of the jaw
H Katsarelis1, N P Shah1, D K Dhariwal1
1Department of Oral and Maxillofacial Surgery, John Radcliffe Hospital, Oxford, UK.
Abstract:
Medication-related osteonecrosis of the jaw (MRONJ), although initially believed to be exclusively associated with bisphosphonates, has been implicated in recent reports with additional drugs, especially the bone antiresorptive denosumab. The pathophysiology has not been fully elucidated, and no causal association between bone antiresorptive regimens and MRONJ has yet been established. However, reduced bone turnover and infection, an almost universal finding, are thought to be central to the pathogenesis of MRONJ. Both bisphosphonates and denosumab, through different pathways of action, significantly reduce the rate of bone turnover and potentially reduce the efficacy of the host defense against infection. Recent evidence questions the simplified etiology of low bone turnover causing MRONJ and offers evidence on the prominent role of infection instead. The management of MRONJ remains a significant clinical challenge, with little progress having been made on treatment. The aim of this article is to explore the current theories on the etiology of MRONJ and to emphasize the importance of infection in the development of this devastating pathology.
Insights
Medication-related osteonecrosis of the jaw (MRONJ) is linked to antiresorptive drugs like denosumab. While reduced bone turnover is implicated, recent evidence highlights the critical role of infection in MRONJ development.
Area of Science:
- Oral and Maxillofacial Surgery
- Pharmacology
- Infectious Diseases
Background:
- Medication-related osteonecrosis of the jaw (MRONJ) was initially linked to bisphosphonates but is now associated with other antiresorptives like denosumab.
- The exact cause of MRONJ is not fully understood, and a direct link to bone antiresorptive drugs remains unproven.
Purpose of the Study:
- To explore current theories on MRONJ etiology.
- To emphasize the significant role of infection in MRONJ pathogenesis.
Main Methods:
- Review of current scientific literature on MRONJ.
- Analysis of proposed pathophysiological mechanisms.
Main Results:
- Reduced bone turnover and infection are considered central to MRONJ pathogenesis.
- Both bisphosphonates and denosumab decrease bone turnover and may impair infection defense.
- Emerging evidence suggests infection plays a more prominent role than previously thought, challenging the low bone turnover hypothesis.
Conclusions:
- Infection is a crucial factor in the development of Medication-related osteonecrosis of the jaw.
- Further research is needed to fully elucidate MRONJ pathophysiology and improve treatment strategies.
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