Poewe W, Gauthier S, Aarsland D, Leverenz J B, Barone P, Weintraub D, Tolosa E, Dubois B
Department of Neurology, Medical University Innsbruck, Innsbruck, Austria.
Int J Clin Pract. 2008 Oct;62(10):1581-7. doi: 10.1111/j.1742-1241.2008.01869.x.
Parkinson's disease (PD) has long been considered predominantly a motor disorder. However, its frequent association with dementia, which contributes significantly to the morbidity and mortality of the condition, is gaining increasing recognition. PD dementia (PDD) has a unique clinical profile and neuropathology, distinct from Alzheimer's disease (AD). Cholinergic deficits, a feature of both AD and PDD, underlie the rationale for cholinesterase inhibitor therapy in both conditions. In clinical practice, it is important that PDD should be recognised and appropriately treated. This review aims to outline the recently proposed clinical diagnostic criteria for PDD and to summarise the guidelines/recommendations published since 2006 on the use of cholinesterase inhibitors in the management of PDD. Although the cholinesterase inhibitor rivastigmine has recently been approved for the management of PDD, there remains a need for the development of novel therapies that can affect key mechanisms of the disease or prevent/delay patients with PD and mild cognitive impairment from progressing to PDD.
帕金森病(PD)长期以来一直被认为主要是一种运动障碍。然而,它与痴呆症的频繁关联日益受到关注,痴呆症对该疾病的发病率和死亡率有显著影响。帕金森病痴呆(PDD)具有独特的临床特征和神经病理学,与阿尔茨海默病(AD)不同。胆碱能缺陷是AD和PDD的共同特征,这是两种疾病中使用胆碱酯酶抑制剂治疗的理论基础。在临床实践中,识别并适当治疗PDD很重要。本综述旨在概述最近提出的PDD临床诊断标准,并总结自2006年以来发表的关于在PDD管理中使用胆碱酯酶抑制剂的指南/建议。尽管胆碱酯酶抑制剂卡巴拉汀最近已被批准用于PDD的管理,但仍需要开发能够影响该疾病关键机制或预防/延缓帕金森病和轻度认知障碍患者进展为PDD的新疗法。