Pediatric Neurology and Muscular Diseases Unit, IRCCS 'G.Gaslini' Institute, Genoa, Italy.
Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, and Maternal and Child Health, University of Genoa, Genoa, Italy.
Expert Rev Neurother. 2020 Apr;20(4):341-350. doi: 10.1080/14737175.2020.1741350. Epub 2020 Mar 17.
: Progressive myoclonus epilepsies (PMEs) are a group of neurodegenerative diseases, invariably leading to severe disability or fatal outcome in a few years or decades. Nowadays, PMEs treatment remains challenging with a significant burden of disability for patients. Pharmacotherapy is primarily used to treat seizures, which impact patients' quality of life. However, new approaches have emerged in the last few years, which try to curb the neurological deterioration of PMEs through a better knowledge of the pathogenetic process. This is a review on the newest therapeutic options for the treatment of PMEs.: Experimental and clinical results on novel therapeutic approaches for the different forms of PME are reviewed and discussed. Special attention is primarily focused on the efficacy and tolerability outcomes, trying to infer the role novel approaches may have in the future.: The large heterogeneity of disease-causing mechanisms prevents researchers from identifying a single approach to treat PMEs. Understanding of pathophysiologic processes is leading the way to targeted therapies, which, through enzyme replacement or underlying gene defect correction have already proved to potentially strike on neurodegeneration.
进行性肌阵挛性癫痫(PMEs)是一组神经退行性疾病,在几年或几十年内不可避免地导致严重残疾或致命后果。如今,PMEs 的治疗仍然具有挑战性,给患者带来了严重的残疾负担。药物治疗主要用于治疗癫痫发作,这会影响患者的生活质量。然而,在过去几年中出现了新的方法,试图通过更好地了解发病机制来遏制 PMEs 的神经恶化。这是一篇关于治疗 PMEs 的最新治疗选择的综述。本文综述和讨论了针对不同形式 PME 的新型治疗方法的实验和临床结果。主要关注的是疗效和耐受性结果,试图推断新方法在未来可能发挥的作用。疾病机制的巨大异质性使得研究人员无法确定一种单一的方法来治疗 PMEs。对病理生理过程的理解为靶向治疗开辟了道路,通过酶替代或潜在的基因缺陷纠正,已经证明有可能对抗神经退行性变。