摘要
多系统萎缩(MSA)是一种成年发病的进行性的神经系统变性病,可分为帕金森型(MSA-P)和小脑型(MSA-C),临床表现为快速进展的自主神经功能障碍和运动功能障碍。MSA的病因尚不清楚,多种致病因素参与MSA发病,因此除了有限的对症治疗外,尚缺乏疾病修饰疗法以阻止疾病进展。目前,靶向α突触核蛋白、神经炎症和神经营养支持的动物和临床研究正在探索中,现就最新进展进行综述,以期提高临床对MSA精准化治疗的认识。
Multiple system atrophy(MSA)is an adult-onset and progressive neurodegenerative disease,is clinically classified into two subtypes:MSA with predominant parkinsonism(MSA-P)and MSA with predominant cerebellar ataxia(MSA-C),characterized by dysautonomia and dyskinesia.The etiology of MSA is still unknown,multiple pathogenic factors are involved in the pathogenesis of this disease,therefore,in addition to limited symptomatic treatment,there is still a lack of disease modifying therapy to prevent the progress of the disease.Currently,animal and clinical studies targeting α-synuclein,neuroinflammation and neurotrophic supporting are being explored,so this article reviewed the latest progresses to improve the clinical understanding of treatment of MSA.
作者
张含
李楠楠
张新宁
王垚
周莹
李亚楠
阎明源
陈志刚
ZHANG Han;LI Nannan;ZHANG Xinning(The Second Clinical School of Beijing University of Chinese Medicine,Beijing 100029,China)
出处
《临床神经病学杂志》
CAS
2023年第6期474-479,共6页
Journal of Clinical Neurology
基金
国家自然科学基金项目(82174328)
首都卫生发展科研专项项目(首发2018-2-4202)。
关键词
多系统萎缩
靶向治疗
Α突触核蛋白
研究进展
multiple system atrophy
targeted therapy
α-synuclein
research progress