Chen BaoLing, Yang Wanlin, Luo Yuqi, Tan Eng-King, Wang Qing
Department of Neurology, Zhujiang Hospital, Southern Medical University, Gongye Road 253, Guangzhou, 510282, Guangdong, People's Republic of China.
Department of Neurology, National Neuroscience Institute, Singapore General Hospital, Singapore, Singapore.
J Neurol. 2023 Nov;270(11):5251-5273. doi: 10.1007/s00415-023-11876-y. Epub 2023 Jul 21.
Multiple system atrophy (MSA) is a sporadic, fatal, and rapidly progressive neurodegenerative disease of unknown etiology that is clinically characterized by autonomic failure, parkinsonism, cerebellar ataxia, and pyramidal signs in any combination. Early onset and extensive autonomic dysfunction, including cardiovascular dysfunction characterized by orthostatic hypotension (OH) and supine hypertension, urinary dysfunction characterized by overactive bladder and incomplete bladder emptying, sexual dysfunction characterized by sexual desire deficiency and erectile dysfunction, and gastrointestinal dysfunction characterized by delayed gastric emptying and constipation, are the main features of MSA. Autonomic dysfunction greatly reduces quality of life and increases mortality. Therefore, early diagnosis and intervention are urgently needed to benefit MSA patients. In this review, we aim to discuss the systematic treatment of autonomic dysfunction in MSA, and focus on the current methods, starting from non-pharmacological methods, such as patient education, psychotherapy, diet change, surgery, and neuromodulation, to various drug treatments targeting autonomic nerve and its projection fibers. In addition, we also draw attention to the interactions among various treatments, and introduce novel methods proposed in recent years, such as gene therapy, stem cell therapy, and neural prosthesis implantation. Furthermore, we elaborate on the specific targets and mechanisms of action of various drugs. We would like to call for large-scale research to determine the efficacy of these methods in the future. Finally, we point out that studies on the pathogenesis of MSA and pathophysiological mechanisms of various autonomic dysfunction would also contribute to the development of new promising treatments and concepts.
多系统萎缩(MSA)是一种散发的、致命的、快速进展的病因不明的神经退行性疾病,临床特征为自主神经功能衰竭、帕金森综合征、小脑共济失调和锥体束征,可任意组合出现。早发且广泛的自主神经功能障碍是MSA的主要特征,包括以直立性低血压(OH)和卧位高血压为特征的心血管功能障碍、以膀胱过度活动症和膀胱排空不全为特征的泌尿功能障碍、以性欲减退和勃起功能障碍为特征的性功能障碍,以及以胃排空延迟和便秘为特征的胃肠功能障碍。自主神经功能障碍极大地降低了生活质量并增加了死亡率。因此,迫切需要早期诊断和干预以造福MSA患者。在本综述中,我们旨在探讨MSA自主神经功能障碍的系统治疗方法,重点关注当前的方法,从非药物方法,如患者教育、心理治疗、饮食改变、手术和神经调节,到针对自主神经及其投射纤维的各种药物治疗。此外,我们还关注各种治疗方法之间的相互作用,并介绍近年来提出的新方法,如基因治疗、干细胞治疗和神经假体植入。此外,我们详细阐述了各种药物的具体靶点和作用机制。我们呼吁开展大规模研究以确定这些方法未来的疗效。最后,我们指出,对MSA发病机制和各种自主神经功能障碍病理生理机制的研究也将有助于开发新的有前景的治疗方法和理念。