Tröster Alexander I
Department of Neurology (CB 7025), University of North Carolina at Chapel Hill, 3114 Bioinformatics Building, Chapel Hill, NC 27599-7025, USA.
Neuropsychol Rev. 2008 Mar;18(1):103-19. doi: 10.1007/s11065-008-9055-0. Epub 2008 Mar 6.
Parkinson's disease with dementia (PDD) and dementia with Lewy bodies (DLB) are neurodegenerative conditions sharing a disorder of alpha-synuclein metabolism. Temporal differences in the emergence of symptoms and clinical features warrant the continued clinical distinction between DLB and PDD. While DLB and PDD groups' neuropsychological profiles often differ from those in Alzheimer's disease (AD), the diagnostic sensitivity, specificity, and predictive values of these profiles remain largely unknown. PDD and DLB neuropsychological profiles share sufficient similarity to resist accurate and reliable differentiation. Although heterogeneous cognitive changes (predominantly in memory and executive function) may manifest earlier and more frequently than previously appreciated in Parkinson's disease (PD), and executive deficits may be harbingers of dementia, the enthusiasm to uncritically extend the concept of mild cognitive impairment (MCI) to PD should be tempered. Instead, future research might strive to identify the precise neuropsychological characteristics of the prodromal stages of PD, PDD, and DLB which, in conjunction with other potential biomarkers, facilitate early and accurate diagnosis, and the definition of neuroprotective, neurorestorative, and symptomatic treatment endpoints.
帕金森病痴呆(PDD)和路易体痴呆(DLB)是神经退行性疾病,都存在α-突触核蛋白代谢紊乱。症状和临床特征出现的时间差异使得DLB和PDD在临床上仍需加以区分。虽然DLB和PDD组的神经心理学特征通常与阿尔茨海默病(AD)不同,但这些特征的诊断敏感性、特异性和预测价值在很大程度上仍不清楚。PDD和DLB的神经心理学特征有足够的相似性,难以进行准确可靠的区分。尽管异质性认知变化(主要在记忆和执行功能方面)在帕金森病(PD)中可能比以前认为的更早、更频繁地出现,并且执行功能缺陷可能是痴呆的先兆,但不加批判地将轻度认知障碍(MCI)概念扩展到PD的热情应有所收敛。相反,未来的研究可能会努力确定PD、PDD和DLB前驱期的确切神经心理学特征,这些特征与其他潜在生物标志物一起,有助于早期准确诊断,以及神经保护、神经修复和症状性治疗终点的定义。