Department of Head and Neck Oncology, State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Department of Dental and Alveolar Surgery, State Key Laboratory of Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Int J Oral Maxillofac Surg. 2020 Mar;49(3):298-309. doi: 10.1016/j.ijom.2019.07.016. Epub 2019 Aug 22.
Medication-related osteonecrosis of the jaw (MRONJ) is a severe complication that can develop in patients treated with anti-resorptive drugs. Although the pathogenesis of MRONJ is still unclear, genetic factors have a demonstrated important role. Thus, the aim of this study was to perform a systematic review on the pharmacogenetics of MRONJ. Studies published until March 2019 were retrieved from eight databases and were selected by two independent reviewers. Evidence on several genetic polymorphisms was summarized and a meta-analysis was conducted when possible. Fourteen studies involving 1515 participants were eligible for systematic review. For CYP2C8 rs1934951, no significant difference was observed between the MRONJ and non-MRONJ groups (odds ratio (OR) 2.04, 95% confidence interval (CI) 0.88-4.73, P=0.09). However, a subgroup analysis based on only multiple myeloma status showed a positive association (OR 3.64, 95% CI 1.29-10.30, P=0.01). PPARG rs1152003 was not differently distributed between groups (OR 0.25, 95% CI 0.01-9.92, P=0.46). Also, VEGF rs3025039 was found to be correlated with the occurrence of MRONJ (OR 0.35, 95% CI 0.15-0.82, P=0.02). CYP2C8 rs1934951 (in multiple myeloma patients) and VEGF rs3025039 are associated with the development of MRONJ in patients treated with bisphosphonates. The results are promising and call for new trials with a larger sample to further explore this growing field.
药物相关性下颌骨坏死(MRONJ)是一种严重的并发症,可发生在接受抗吸收药物治疗的患者中。虽然 MRONJ 的发病机制尚不清楚,但遗传因素已被证明具有重要作用。因此,本研究旨在对 MRONJ 的药物遗传学进行系统评价。从 8 个数据库中检索到截至 2019 年 3 月发表的研究,并由两名独立的审查员进行选择。总结了几项遗传多态性的证据,并在可能的情况下进行了荟萃分析。有 14 项研究涉及 1515 名参与者符合系统评价的标准。对于 CYP2C8 rs1934951,MRONJ 组和非 MRONJ 组之间无显著差异(比值比(OR)2.04,95%置信区间(CI)0.88-4.73,P=0.09)。然而,仅基于多发性骨髓瘤状态的亚组分析显示出阳性关联(OR 3.64,95%CI 1.29-10.30,P=0.01)。PPARG rs1152003 在两组之间的分布无差异(OR 0.25,95%CI 0.01-9.92,P=0.46)。此外,VEGF rs3025039 与 MRONJ 的发生相关(OR 0.35,95%CI 0.15-0.82,P=0.02)。CYP2C8 rs1934951(多发性骨髓瘤患者)和 VEGF rs3025039 与接受双膦酸盐治疗的患者中 MRONJ 的发生相关。结果有希望,并呼吁进行更大样本量的新试验,以进一步探索这一不断发展的领域。