Department of Health Sciences, University "Magna Graecia" of Catanzaro, 88100 Catanzaro, Italy.
Pharmacotechnology Documentation and Transfer Unit, Preclinical and Translational Pharmacology, Department of Pharmacy, Health and Nutritional Sciences, University of Calabria, 87036 Rende, Italy.
Toxins (Basel). 2023 May 12;15(5):332. doi: 10.3390/toxins15050332.
Some 14% of global prevalence, based on high-income country populations, suffers from migraine. Chronic migraine is very disabling, being characterized by at least 15 headache days per month of which at least 8 days present the features of migraine. Onabotulinumtoxin A, targeting the machinery for exocytosis of neurotransmitters and neuropeptides, has been approved for use in chronic migraine since 2010. This systematic review and meta-analysis appraises the safety of onabotulinumtoxin A treatment for chronic migraine and the occurrence of treatment-related adverse events (TRAEs) in randomized, clinical studies in comparison with placebo or other comparators and preventative treatments according to the most updated Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) 2020 recommendations. The search retrieved 888 total records. Nine studies are included and seven were eligible for meta-analysis. The present study demonstrates that toxin produces more TRAEs than placebo, but less than oral topiramate, supporting the safety of onabotulinumtoxin A, and highlights the heterogeneity of the studies present in the literature (I = 96%; < 0.00001). This points to the need for further, adequately powered, randomized clinical trials assessing the safety of onabotulinumtoxin A in combination with the newest treatment options.
根据高收入国家的人口数据,全球约有 14%的人患有偏头痛。慢性偏头痛非常致残,其特征是每月至少有 15 天头痛,其中至少有 8 天具有偏头痛的特征。自 2010 年以来,肉毒杆菌毒素 A(一种针对神经递质和神经肽胞吐机制的药物)已被批准用于慢性偏头痛的治疗。本系统评价和荟萃分析根据最新的系统评价和荟萃分析报告的首选条目(PRISMA)2020 建议,评估了肉毒杆菌毒素 A 治疗慢性偏头痛的安全性以及与安慰剂或其他对照药物和预防治疗相关的不良事件(TRAEs)的发生情况。检索到 888 条总记录。共纳入 9 项研究,其中 7 项研究符合荟萃分析条件。本研究表明,肉毒毒素产生的 TRAEs 比安慰剂多,但比口服托吡酯少,支持肉毒杆菌毒素 A 的安全性,并强调了文献中研究的异质性(I = 96%;<0.00001)。这表明需要进一步进行充分的、随机的临床试验,以评估肉毒杆菌毒素 A 与最新治疗方案联合应用的安全性。