Novo Pereira Ines, De la Torre Canales Giancarlo, Durão Sara, Shado Rawand, Braga Ana Cristina, Almeida André Mariz, Hassan Haidar, Manso Ana Cristina, Faria-Almeida Ricardo
Faculty of Dental Medicine, University of Porto (FMDUP), Rua Dr. Manuel Pereira da Silva, 4200-393 Porto, Portugal.
Egas Moniz Center for Interdisciplinary Research, Egas Moniz School of Health & Science, 2829-511 Almada, Portugal.
Toxins (Basel). 2025 Jul 29;17(8):377. doi: 10.3390/toxins17080377.
Current research reported that the number of clinical studies found for botulinum toxin (BoNT) key effects on biochemical biomarkers in head and neck chronic conditions linked to inflammation was very low. There are no systematic reviews of animal studies on this topic, and hence our review aimed to evaluate the quality of the preclinical evidence. We searched PubMed, Scopus, and Web of Science databases, and registries up to 29 January 2024. There were 22 eligible records, and data were available for 11 randomised controlled trials. There were concerns about the risk of bias and great variations of data obtained regarding chronic conditions, which included mostly trigeminal neuralgia. The leading biomarkers were proinflammatory cytokines (IL-1β, TNF-α) and synaptosomal-associated protein-25 (SNAP25), followed by neuron activation marker c-Fos and calcitonin gene-related peptide (CGRP). Overall, data found that BoNT significantly altered the under/over-expression of biomarkers evoked by the investigated disease models and had no effect when the levels of these biomarkers were not changed by the induced chronic conditions in animals. However, there were some mixed results and exceptions, and the certainty evidence found was very low to low. Although the sample sizes detected significant effect size ( < 0.05), most studies are based on male inferior animals, which may limit the recommendations for clinical trials. This study is registered on PROSPERO (CRD42023432411).
当前研究报告称,关于肉毒杆菌毒素(BoNT)对与炎症相关的头颈慢性疾病生化生物标志物的关键作用,所发现的临床研究数量非常少。目前尚无关于该主题的动物研究的系统综述,因此我们的综述旨在评估临床前证据的质量。我们检索了截至2024年1月29日的PubMed、Scopus和Web of Science数据库以及注册库。共有22条符合条件的记录,其中11项随机对照试验的数据可用。对于慢性疾病(主要包括三叉神经痛),存在偏倚风险以及所获得数据差异很大的问题。主要的生物标志物是促炎细胞因子(IL-1β、TNF-α)和突触体相关蛋白25(SNAP25),其次是神经元激活标记物c-Fos和降钙素基因相关肽(CGRP)。总体而言,数据表明BoNT显著改变了所研究疾病模型诱发的生物标志物的表达不足/过度表达,而当这些生物标志物的水平未因动物诱导的慢性疾病而改变时则没有效果。然而,存在一些混合结果和例外情况,所发现的确凿证据非常低到低。尽管样本量检测到显著的效应大小(<0.05),但大多数研究基于雄性低等动物,这可能会限制对临床试验的建议。本研究已在PROSPERO(CRD42023432411)上注册。