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帕金森病非运动症状的神经病理生物学

Neuropathobiology of non-motor symptoms in Parkinson disease.

作者信息

Jellinger Kurt A

机构信息

Institute of Clinical Neurobiology, Kenyongasse 18, 1070, Vienna, Austria.

出版信息

J Neural Transm (Vienna). 2015 Oct;122(10):1429-40. doi: 10.1007/s00702-015-1405-5. Epub 2015 May 15.

Abstract

Parkinson disease (PD) is a multisystem disorder associated with α-synuclein aggregates throughout the central, autonomic, and peripheral nervous system, clinically characterized by motor and non-motor (NM) symptoms. The NMS in PD, many of which antedating motor dysfunction and representing a preclinical phase spanning 20 or more years, are linked to widespread distribution of α-synuclein pathology not restricted to the dopaminergic nigrostriatal system that is responsible for core motor features of PD. The pathologic substrate of NM manifestations such as olfactory, autonomic (gastrointestinal, urogenital, cardia, respiratory), sensory, skin, sleep, visual, neuropsychiatric dysfunctions (cognitive, mood, dementia), and others are critically reviewed. In addition to non-nigral brainstem nuclei, α-synuclein pathology involves sympathetic and parasympathetic, enteric, cardiac and pelvic plexuses, and many other organs indicating a topographical and chronological spread, particularly in the prodromal stages of the disease. Few animal models recapitulate NMS in PD. The relationship between regional α-synuclein/Lewy pathology, neurodegeneration and the corresponding clinical deficits awaits further elucidation. Controlled clinicopathologic studies will refine the correlations between presymptomatic and late-developing NM features of PD and neuropathology, and new premotor biomarkers will facilitate early diagnosis of PD as a basis for more effective preventive and therapeutic options of this devastating disease.

摘要

帕金森病(PD)是一种多系统疾病,与整个中枢、自主和外周神经系统中的α-突触核蛋白聚集有关,临床特征为运动和非运动(NM)症状。PD中的非运动症状,其中许多早于运动功能障碍,代表了一个长达20年或更长时间的临床前期,与α-突触核蛋白病理的广泛分布有关,这种分布不限于负责PD核心运动特征的多巴胺能黑质纹状体系统。对嗅觉、自主神经(胃肠、泌尿生殖、心脏、呼吸)、感觉、皮肤、睡眠、视觉、神经精神功能障碍(认知、情绪、痴呆)等非运动表现的病理基础进行了严格审查。除了非黑质脑干核,α-突触核蛋白病理还涉及交感和副交感神经、肠、心脏和盆腔神经丛,以及许多其他器官,表明存在拓扑和时间上的扩散,特别是在疾病的前驱阶段。很少有动物模型能重现PD中的非运动症状。区域α-突触核蛋白/路易体病理、神经退行性变与相应临床缺陷之间的关系有待进一步阐明。对照的临床病理研究将完善PD症状前和后期出现的非运动特征与神经病理学之间的相关性,新的运动前生物标志物将有助于PD的早期诊断,作为对这种毁灭性疾病采取更有效预防和治疗方案的基础。

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