Biundo Roberta, Weis Luca, Antonini Angelo
Parkinson's Disease and Movement Disorder Department, "IRCCS, San Camillo" Rehabilitation Hospital, Venice-Lido, Italy.
NPJ Parkinsons Dis. 2016 Sep 1;2:16018. doi: 10.1038/npjparkd.2016.18. eCollection 2016.
Mild cognitive impairment (PD-MCI) and dementia (PDD) are among the most frequent non-motor symptoms in Parkinson's disease (PD). PD-MCI is six times more likely than age-matched controls to develop dementia and the PDD prevalence is 80% after 15-20 years of disease. Therefore, research has focused on the identification of early dementia biomarkers including specific cognitive at-risk profiles hoping to implement therapeutic interventions when they are most likely to be efficacious. However, given the heterogeneous neuropathological, neurochemical, and neuropsychological nature of cognitive deficits, definition of a comprehensive cognitive model of PDD is a challenge. Evidence from neuroimaging studies using different methods and techniques suggests that in addition to degeneration of the dopaminergic system, other mechanisms have a role including β-amyloid and tau deposition, and that specific cognitive scales could help identifying a malignant profile. Prospective studies combining neuroimaging techniques and specific cognitive tests are required to define the interplay between the various neurodegenerative processes and the contribution of structural disconnection in brain functional networks, heralding the development of dementia in PD.
轻度认知障碍(帕金森病所致轻度认知障碍,PD-MCI)和痴呆(帕金森病痴呆,PDD)是帕金森病(PD)最常见的非运动症状。与年龄匹配的对照组相比,PD-MCI发展为痴呆的可能性高出6倍,且在患病15 - 20年后,PDD的患病率为80%。因此,研究集中于识别早期痴呆生物标志物,包括特定的认知风险特征,以期在最有可能有效的时候实施治疗干预。然而,鉴于认知缺陷在神经病理学、神经化学和神经心理学方面具有异质性,定义一个全面的PDD认知模型是一项挑战。使用不同方法和技术的神经影像学研究证据表明,除了多巴胺能系统退化外,其他机制也起作用,包括β-淀粉样蛋白和tau蛋白沉积,且特定的认知量表有助于识别恶性特征。需要结合神经影像学技术和特定认知测试的前瞻性研究来确定各种神经退行性过程之间的相互作用以及脑功能网络中结构断开的作用,这预示着PD中痴呆的发展。