Paulo Victor Alves de Sales, Isabella Piassi Dias Godói, Gerly Anne de Castro Brito, Renata Carvalho Leitão, Aurigena Antunes de Araújo, Caroline Addison Carvalho Xavier de Medeiros
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Risk of bias was assessed using RoB 2.0 and ROBINS-I tools.</p><p><strong>Results: </strong>A total of 355 studies was identified. After the screening, seven met the eligibility criteria. The RCTs showed a low risk of bias. PBMT reduced OM incidence in patients undergoing chemotherapy/radiotherapy. PBMT decreased pro-inflammatory cytokines (interleukin-6, tumor necrosis factor-α) and increased anti-inflammatory cytokines (interleukin-4, interleukin-10). It also modulated inflammatory mediators, enhancing the antioxidant enzyme superoxide dismutase and overexpressing genes for keratinocyte differentiation, aiding injury repair.</p><p><strong>Conclusion: </strong>The findings suggested that the mechanism of action of PBMT in OM involves modulation of the inflammatory response, balancing oxygen reactive species generation, and expression of factors related to healing or repair. 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引用次数: 0
摘要
目的:对光生物调节疗法(PBMT)治疗或预防抗肿瘤治疗引起的口腔黏膜炎(OM)的机制进行系统综述。方法:根据PRISMA 2020指南,于2023年8月至9月在Medline、拉丁美洲和加勒比健康科学文献(LILACS)、科学电子图书馆在线(SciELO)和Bibliografia Brasileira de Odontologia中检索与OM和激光治疗相关的描述词。综述了光生物调节机理的研究进展。回顾了过去10年的随机(rct)或非随机试验。使用rob2.0和ROBINS-I工具评估偏倚风险。结果:共确定了355项研究。经过筛选,有7人符合资格标准。随机对照试验显示偏倚风险较低。PBMT降低了化疗/放疗患者OM的发病率。PBMT降低促炎细胞因子(白细胞介素-6、肿瘤坏死因子-α),增加抗炎细胞因子(白细胞介素-4、白细胞介素-10)。它还可以调节炎症介质,增强抗氧化酶超氧化物歧化酶和角化细胞分化基因的过表达,帮助损伤修复。结论:PBMT在OM中的作用机制包括调节炎症反应,平衡氧反应物质的产生,以及与愈合或修复相关因子的表达。需要进一步的研究来阐明这些机制并优化治疗方案。
Mechanisms of photobiomodulation therapy in treating and preventing antineoplastic-induced oral mucositis: a systematic review.
Purpose: To conduct a systematic review of the mechanisms of photobiomodulation therapy (PBMT) for treating or preventing oral mucositis (OM) caused by antineoplastic therapy.
Methods: Following PRISMA 2020 guidelines, a search was conducted in Medline, Latin American and Caribbean Health Sciences Literature (LILACS), Scientific Electronic Library Online (SciELO), and Bibliografia Brasileira de Odontologia from August to September 2023 using descriptors related to OM and laser therapy. Studies on the mechanisms of photobiomodulation in OM were included. Randomized (RCTs) or non-randomized trials from the past 10 years were reviewed. Risk of bias was assessed using RoB 2.0 and ROBINS-I tools.
Results: A total of 355 studies was identified. After the screening, seven met the eligibility criteria. The RCTs showed a low risk of bias. PBMT reduced OM incidence in patients undergoing chemotherapy/radiotherapy. PBMT decreased pro-inflammatory cytokines (interleukin-6, tumor necrosis factor-α) and increased anti-inflammatory cytokines (interleukin-4, interleukin-10). It also modulated inflammatory mediators, enhancing the antioxidant enzyme superoxide dismutase and overexpressing genes for keratinocyte differentiation, aiding injury repair.
Conclusion: The findings suggested that the mechanism of action of PBMT in OM involves modulation of the inflammatory response, balancing oxygen reactive species generation, and expression of factors related to healing or repair. Further studies are needed to elucidate these mechanisms and optimize treatment protocols.