Cookson Mark R, Hardy John, Lewis Patrick A
Laboratory of Neurogenetics, National Institute on Aging, Bethesda MD, USA.
Int J Clin Exp Pathol. 2008 Jan 1;1(3):217-31.
Parkinson's disease (PD) has long been considered to be a sporadic entity, perhaps with an environmental etiology. However, recent genetic discoveries have challenged this view, as there are many families with diseases of Mendelian inheritance that clinically resemble PD. Here, we will review in detail the neuropathological data relating to familial cases of PD. We will discuss the complicated relationships between the genetically defined cases and the two key pathological events seen in PD, namely loss of dopaminergic neurons in the substantia nigra pars compacta and the formation of protein inclusions, Lewy bodies, in the neurons that survive to the end stage of the disease course. These observations will be synthesized into an overall scheme that emphasizes the two key aspects of the neuropathology as distinct events and suggest that each gene tells us something a little different about the neuropathology of PD.
长期以来,帕金森病(PD)一直被认为是一种散发性疾病,可能由环境因素引发。然而,最近的遗传学发现对这一观点提出了挑战,因为有许多符合孟德尔遗传规律的家族性疾病,其临床症状与帕金森病相似。在此,我们将详细回顾与帕金森病家族性病例相关的神经病理学数据。我们将讨论基因明确的病例与帕金森病中两个关键病理事件之间的复杂关系,即黑质致密部多巴胺能神经元的丧失以及在疾病进程末期存活的神经元中蛋白质包涵体(路易小体)的形成。这些观察结果将被整合到一个总体框架中,该框架强调神经病理学的这两个关键方面是不同的事件,并表明每个基因都能让我们对帕金森病的神经病理学有一些不同的了解。