Halliday Glenda M, Leverenz James B, Schneider Jay S, Adler Charles H
Neuroscience Research Australia and the University of New South Wales, Sydney, Australia.
Mov Disord. 2014 Apr 15;29(5):634-50. doi: 10.1002/mds.25857.
The recent formalization of clinical criteria for Parkinson's disease with dementia (PDD) codifies many studies on this topic, including those assessing biological correlates. These studies show that the emergence of PDD occurs on the background of severe dopamine deficits with, the main pathological drivers of cognitive decline being a synergistic effect between alpha-synuclein and Alzheimer's disease pathology. The presence of these pathologies correlates with a marked loss of limbic and cortically projecting dopamine, noradrenaline, serotonin, and acetylcholine neurons, although the exact timing of these relationships remains to be determined. Genetic factors, such as triplications in the α-synuclein gene, lead to a clear increased risk of PDD, whereas others, such as parkin mutations, are associated with a reduced risk of PDD. The very recent formalization of clinical criteria for PD with mild cognitive impairment (PD-MCI) allows only speculation on its biological and genetic bases. Critical assessment of animal models shows that chronic low-dose MPTP treatment in primates recapitulates PD-MCI over time, enhancing the current biological concept of PD-MCI as having enhanced dopamine deficiency in frontostriatal pathways as well as involvement of other neurotransmitter systems. Data from other animal models support multiple transmitter involvement in cognitive impairment in PD. Whereas dopamine dysfunction has been highlighted because of its obvious role in PD, the role of the other neurotransmitter systems, neurodegenerative pathologies, and genetic factors in PD-MCI remains to be fully elucidated.
帕金森病痴呆(PDD)临床标准的近期正式确定整理了许多关于该主题的研究,包括那些评估生物学相关性的研究。这些研究表明,PDD的出现是在严重多巴胺缺乏的背景下发生的,认知衰退的主要病理驱动因素是α-突触核蛋白与阿尔茨海默病病理之间的协同作用。这些病理状态的存在与边缘系统以及向皮质投射的多巴胺能、去甲肾上腺素能、5-羟色胺能和胆碱能神经元的显著丧失相关,尽管这些关系的确切时间仍有待确定。遗传因素,如α-突触核蛋白基因的三倍体,会导致PDD风险明显增加,而其他因素,如帕金森基因突变,则与PDD风险降低有关。帕金森病伴轻度认知障碍(PD-MCI)临床标准的近期正式确定仅允许对其生物学和遗传基础进行推测。对动物模型的批判性评估表明,灵长类动物长期低剂量MPTP治疗会随着时间推移重现PD-MCI,强化了目前关于PD-MCI的生物学概念,即前额叶纹状体通路中多巴胺缺乏加剧以及其他神经递质系统也参与其中。其他动物模型的数据支持多种神经递质参与帕金森病的认知障碍。尽管多巴胺功能障碍因其在帕金森病中的明显作用而受到关注,但其他神经递质系统、神经退行性病变和遗传因素在PD-MCI中的作用仍有待充分阐明。