Toronto Western Hospital, Movement Disorders Centre, 399 Bathurst St 7 MCL, Toronto, ON M5T 2S8, Canada.
J Neurol Neurosurg Psychiatry. 2013 Apr;84(4):409-15. doi: 10.1136/jnnp-2012-303455. Epub 2012 Sep 5.
Like many neurodegenerative disorders, Parkinson's disease (PD) is clinically highly heterogeneous. A number of studies have proposed and defined subtypes of PD based on clinical features that tend to cluster together. These subtypes present an opportunity to refine studies of aetiology, course and treatment responsiveness in PD, as clinical variability must represent underlying biological or pathophysiological differences between individuals. In this paper, we review what subtypes have been identified in PD and the validation they have undergone. We then discuss what the subtypes could tell us about the disease and how they have been incorporated into studies of aetiology, progression and treatment. Finally, with the knowledge that they have been incorporated very little into PD clinical research, we make recommendations for how subtypes should be used and make some practical recommendations to address this lack of knowledge translation.
与许多神经退行性疾病一样,帕金森病(PD)在临床上具有高度异质性。许多研究根据倾向于聚集在一起的临床特征提出并定义了 PD 的亚型。这些亚型为 PD 的病因、病程和治疗反应性研究提供了机会,因为临床变异性必须代表个体之间潜在的生物学或病理生理学差异。在本文中,我们回顾了 PD 中已确定的亚型及其经过的验证。然后,我们讨论了这些亚型可以告诉我们关于该疾病的哪些信息,以及它们如何被纳入病因、进展和治疗研究。最后,鉴于它们很少被纳入 PD 临床研究,我们就如何使用亚型提出了建议,并提出了一些实用的建议来解决这一知识转化的缺乏。