Valera Elvira, Masliah Eliezer
Department of Neurosciences, University of California, San Diego, La Jolla, California, USA.
Department of Pathology, University of California, San Diego, La Jolla, California, USA.
J Neurochem. 2016 Oct;139 Suppl 1(Suppl 1):346-352. doi: 10.1111/jnc.13529. Epub 2016 Feb 10.
The lack of effective therapies for neurodegenerative disorders is one of the most relevant challenges of this century, considering that, as the global population ages, the incidence of these type of diseases is quickly on the rise. Among these disorders, synucleinopathies, which are characterized by the abnormal accumulation and spreading of the synaptic protein alpha-synuclein in the brain, already constitute the second leading cause of parkinsonism and dementia in the elderly population. Disorders with alpha-synuclein accumulation include Parkinson's disease, dementia with Lewy bodies and multiple system atrophy. Numerous therapeutic alternatives for synucleinopathies are being tested in pre-clinical models and in the clinic; however, only palliative treatments addressing the dopaminergic deficits are approved to date, and no disease-modifying options are available yet. In this article, we provide a brief overview of therapeutic approaches currently being explored for synucleinopathies, and suggest possible explanations to the clinical trials outcomes. Finally, we propose that a deeper understanding of the pathophysiology of synucleinopathies, together with a combination of therapies tailored to each disease stage, may lead to better therapeutic outcomes in synucleinopathy patients. Synucleinopathies, neurodegenerative disorders characterized by the abnormal accumulation of the protein alpha-synuclein, constitute the second leading cause of parkinsonism and dementia in the elderly population, however, no disease-modifying options are available yet. In this review, we summarize the therapeutic approaches currently being explored for synucleinopathies, suggest possible explanations to the clinical outcomes, and propose areas of further therapeutic improvement. This article is part of a special issue on Parkinson disease.
鉴于随着全球人口老龄化,这类疾病的发病率迅速上升,神经退行性疾病缺乏有效治疗方法是本世纪最严峻的挑战之一。在这些疾病中,突触核蛋白病以大脑中突触蛋白α-突触核蛋白的异常积累和扩散为特征,已经成为老年人群帕金森综合征和痴呆症的第二大主要病因。伴有α-突触核蛋白积累的疾病包括帕金森病、路易体痴呆和多系统萎缩。目前,许多针对突触核蛋白病的治疗方案正在临床前模型和临床试验中进行测试;然而,迄今为止,仅批准了针对多巴胺能缺陷的姑息治疗方法,尚无疾病修饰治疗方案。在本文中,我们简要概述了目前正在探索的针对突触核蛋白病的治疗方法,并对临床试验结果提出了可能的解释。最后,我们提出,深入了解突触核蛋白病的病理生理学,结合针对每个疾病阶段的联合治疗,可能会为突触核蛋白病患者带来更好的治疗效果。突触核蛋白病是以蛋白质α-突触核蛋白异常积累为特征的神经退行性疾病,是老年人群帕金森综合征和痴呆症的第二大主要病因,然而,目前尚无疾病修饰治疗方案。在本综述中,我们总结了目前正在探索的针对突触核蛋白病的治疗方法,对临床结果提出了可能的解释,并提出了进一步治疗改进的领域。本文是关于帕金森病的特刊的一部分。