Suryani Isti Rahayu, Ahmadzai Iraj, That Minh Ton, Shujaat Sohaib, Jacobs Reinhilde
OMFS IMPATH Research Group, Department of Oral and Maxillofacial Surgery and Imaging and Pathology, Faculty of Medicine, University Hospitals Leuven, KU Leuven, Leuven, Belgium.
Department of Dentomaxillofacial Radiology, Faculty of Dentistry, Universitas Gadjah Mada, Yogyakarta, Indonesia.
Front Med (Lausanne). 2023 Aug 31;10:1164051. doi: 10.3389/fmed.2023.1164051. eCollection 2023.
This systematic review was performed to assess the potential influence of medication-induced salivary changes on the development of medication-related osteonecrosis of the jaw (MRONJ).
An electronic search was conducted using PubMed, Web of Science, Cochrane, and Embase databases for articles published up to June 2023. A risk of bias assessment was performed according to the modified Newcastle-Ottawa Scale (NOS). Due to the heterogeneity of the selected studies in relation to the type of medications and outcomes evaluated, a meta-analysis could not be performed.
The initial search revealed 765 studies. Only 10 articles were found to be eligible based on the inclusion criteria that reported on the impact of salivary changes on MRONJ following the administration of different medications. A total of 272 cases of MRONJ (35% women, 32% men, and 32% with no gender reported) with a mean age of 66 years at the time of diagnosis were included. Patients administered with bisphosphonates, steroids, chemotherapy, thalidomide, interferon, and hormone therapy had a significantly higher association between decreased salivary flow and MRONJ occurrence. In addition, bisphosphonates, denosumab, and other bone-modifying agents showed a significantly higher risk of developing MRONJ owing to the changes in salivary microbiome profiles, cytokine profiles, interleukins, hypotaurine, and binding proteins.
The reduction in salivary flow and changes in the concentration of salivary proteins were associated with the development of MRONJ. However, due to the availability of limited evidence, the findings of the review should be interpreted with caution.
https://www.crd.york.ac.uk/PROSPERO/, identifier: CRD42022327645.
进行这项系统评价以评估药物引起的唾液变化对药物相关性颌骨坏死(MRONJ)发生发展的潜在影响。
利用PubMed、科学网、Cochrane和Embase数据库进行电子检索,查找截至2023年6月发表的文章。根据改良的纽卡斯尔 - 渥太华量表(NOS)进行偏倚风险评估。由于所选研究在评估的药物类型和结果方面存在异质性,无法进行荟萃分析。
初步检索发现765项研究。根据纳入标准,仅10篇文章符合要求,这些文章报告了不同药物给药后唾液变化对MRONJ的影响。共纳入272例MRONJ病例(35%为女性,32%为男性,32%未报告性别),诊断时平均年龄为66岁。接受双膦酸盐、类固醇、化疗、沙利度胺、干扰素和激素治疗的患者,唾液流量减少与MRONJ发生之间的关联显著更高。此外,双膦酸盐、地诺单抗和其他骨修饰剂由于唾液微生物组谱、细胞因子谱、白细胞介素、亚牛磺酸和结合蛋白的变化,发生MRONJ的风险显著更高。
唾液流量减少和唾液蛋白浓度变化与MRONJ的发生发展相关。然而,由于现有证据有限,本评价结果应谨慎解读。
PROSPERO评价注册号:https://www.crd.york.ac.uk/PROSPERO/,标识符:CRD42022327645。