Medication-related osteonecrosis of the jaw: A literature review and update

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2022-09-15 DOI:10.1002/dvg.23500
Shinichiro Kuroshima, Farah A. Al-Omari, Muneteru Sasaki, Takashi Sawase
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引用次数: 8

Abstract

Since the initial description of medication-related osteonecrosis of the jaw (MRONJ) almost two decades ago, the potential pathophysiology and risk factors have been elaborated on in many investigations and guidelines. However, the definitive pathophysiology based on scientific evidence remains lacking. Consequently, the optimal clinical treatment and prevention strategies for MRONJ have not been established. Despite their different mechanisms of action, many drugs, including bisphosphonates, denosumab, angiogenesis inhibitors, and other medications, have been reported to be associated with MRONJ lesions in cancer and osteoporosis patients. Importantly, MRONJ occurs predominantly in the jawbones and other craniofacial regions, but not in the appendicular skeleton. In this up-to-date review, the currently available information and theories regarding MRONJ are presented from both clinical and basic science perspectives. The definition and epidemiology of MRONJ, triggering medication, and histopathology are comprehensively summarized. The immunopathology and the potential pathophysiology based on immune cells such as neutrophils, T and B cells, macrophages, dendritic cells, and natural killer cells are also discussed. In addition, antiangiogenesis, soft tissue toxicity, necrotic bone, osteocyte death, and single-nucleotide polymorphisms are examined. Moreover, other possible mechanisms of MRONJ development are considered based on the unique embryological characteristics, different cell behaviors between jawbones and appendicular skeleton, unique anatomical structures, and sustained bacterial exposure in the oral cavity as a basis for MRONJ site specificity. Based on the literature review, it was concluded that multiple factors may contribute to the development of MRONJ, although which one is the key player triggering MRONJ in the craniofacial region remains unknown.

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颌骨药物相关性骨坏死:文献回顾与更新
自20年前药物相关性颌骨骨坏死(MRONJ)的首次描述以来,潜在的病理生理和危险因素已在许多研究和指南中得到阐述。然而,基于科学证据的明确病理生理学仍然缺乏。因此,MRONJ的最佳临床治疗和预防策略尚未建立。尽管它们的作用机制不同,但许多药物,包括双膦酸盐、地诺单抗、血管生成抑制剂和其他药物,已被报道与癌症和骨质疏松症患者的MRONJ病变有关。重要的是,MRONJ主要发生在颌骨和其他颅面区域,而不是在附肢骨骼。在这篇最新的综述中,从临床和基础科学的角度介绍了目前关于MRONJ的信息和理论。综述了MRONJ的定义、流行病学、触发药物、组织病理学。讨论了免疫细胞如中性粒细胞、T细胞和B细胞、巨噬细胞、树突状细胞和自然杀伤细胞的免疫病理和潜在的病理生理。此外,还检查了抗血管生成、软组织毒性、坏死骨、骨细胞死亡和单核苷酸多态性。此外,基于独特的胚胎学特征、颌骨和尾骨之间不同的细胞行为、独特的解剖结构以及口腔中持续的细菌暴露作为MRONJ位点特异性的基础,研究人员还考虑了MRONJ发育的其他可能机制。基于文献综述,我们认为多种因素可能导致MRONJ的发展,但哪一个是触发颅面区MRONJ的关键因素尚不清楚。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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