Jellinger Kurt A
Institute of Clinical Neurobiology, Vienna, Austria.
Free Neuropathol. 2020 Jul 3;1:17. doi: 10.17879/freeneuropathology-2020-2813. eCollection 2020 Jan.
Multiple system atrophy (MSA) is a fatal, adult-onset neurodegenerative disorder of uncertain etiology, clinically characterized by various combinations of Levo-dopa-unresponsive parkinsonism, and cerebellar, motor, and autonomic dysfunctions. MSA is an α-synucleinopathy with specific glioneuronal degeneration involving striatonigral, olivopontocerebellar, autonomic and peripheral nervous systems. The pathologic hallmark of this unique proteinopathy is the deposition of aberrant α-synuclein (αSyn) in both glia (mainly oligodendroglia) and neurons forming pathological inclusions that cause cell dysfunction and demise. The major variants are striatonigral degeneration (MSA with predominant parkinsonism / MSA-P) and olivopontocerebellar atrophy (MSA with prominent cerebellar ataxia / MSA-C). However, the clinical and pathological features of MSA are broader than previously considered. Studies in various mouse models and human patients have helped to better understand the molecular mechanisms that underlie the progression of the disease. The pathogenesis of MSA is characterized by propagation of disease-specific strains of αSyn from neurons to oligodendroglia and cell-to-cell spreading in a "prion-like" manner, oxidative stress, proteasomal and mitochondrial dysfunctions, myelin dysregulation, neuroinflammation, decreased neurotrophic factors, and energy failure. The combination of these mechanisms results in neurodegeneration with widespread demyelination and a multisystem involvement that is specific for MSA. Clinical diagnostic accuracy and differential diagnosis of MSA have improved by using combined biomarkers. Cognitive impairment, which has been a non-supporting feature of MSA, is not uncommon, while severe dementia is rare. Despite several pharmacological approaches in MSA models, no effective disease-modifying therapeutic strategies are currently available, although many clinical trials targeting disease modification, including immunotherapy and combined approaches, are under way. Multidisciplinary research to elucidate the genetic and molecular background of the noxious processes as the basis for development of an effective treatment of the hitherto incurable disorder are urgently needed.
多系统萎缩(MSA)是一种病因不明的致命性成人起病的神经退行性疾病,临床特征为左旋多巴无反应性帕金森综合征、小脑功能障碍、运动功能障碍和自主神经功能障碍的各种组合。MSA是一种α-突触核蛋白病,具有特定的神经胶质神经元变性,累及纹状体黑质、橄榄脑桥小脑、自主神经系统和周围神经系统。这种独特的蛋白病的病理标志是异常α-突触核蛋白(αSyn)在神经胶质细胞(主要是少突胶质细胞)和神经元中沉积,形成导致细胞功能障碍和死亡的病理性包涵体。主要变体为纹状体黑质变性(以帕金森综合征为主的MSA / MSA-P)和橄榄脑桥小脑萎缩(以明显小脑性共济失调为主的MSA / MSA-C)。然而,MSA的临床和病理特征比以前认为的更为广泛。对各种小鼠模型和人类患者的研究有助于更好地理解该疾病进展的分子机制。MSA的发病机制的特征是疾病特异性αSyn毒株以“朊病毒样”方式从神经元传播到少突胶质细胞并在细胞间扩散、氧化应激、蛋白酶体和线粒体功能障碍、髓鞘调节异常、神经炎症、神经营养因子减少和能量衰竭。这些机制的组合导致神经退行性变,并伴有广泛的脱髓鞘和多系统受累,这是MSA所特有的。通过使用联合生物标志物,MSA的临床诊断准确性和鉴别诊断得到了改善。认知障碍在MSA中曾被认为不是支持性特征,但并不少见,而严重痴呆则很少见。尽管在MSA模型中有几种药理学方法,但目前尚无有效的疾病修饰治疗策略,尽管许多针对疾病修饰的临床试验,包括免疫疗法和联合方法,正在进行中。迫切需要进行多学科研究,以阐明有害过程的遗传和分子背景,作为开发有效治疗这种迄今无法治愈疾病的基础。