德诺苏马布
颌骨骨坏死
骨重建
病因学
医学
发病机制
重症监护医学
生物信息学
骨质疏松症
病理
双膦酸盐
内科学
生物
作者
H. Katsarelis,Neha Shah,Daljit Dhariwal,Michael Pazianas
标识
DOI:10.1177/0022034515572021
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI