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Biomarkers for Dementia and Mild Cognitive Impairment in Parkinson's Disease

机译:帕金森氏病痴呆症和轻度认知障碍的生物标志物

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Cognitive decline is one of the most frequent and disabling nonmotor features of Parkinson's disease. Around 30% of patients with Parkinson's disease experience mild cognitive impairment, a well-established risk factor for the development of dementia. However, mild cognitive impairment in patients with Parkinson's disease is a heterogeneous entity that involves different types and extents of cognitive deficits. Because it is not currently known which type of mild cognitive impairment confers a higher risk of progression to dementia, it would be useful to define biomarkers that could identify these patients to better study disease progression and possible interventions. In this sense, the identification among patients with Parkinson's disease and mild cognitive impairment of biomarkers associated with dementia would allow the early detection of this process. This review summarizes studies from the past 25 years that have assessed the potential biomarkers of dementia and mild cognitive impairment in Parkinson's disease patients. Despite the potential importance, no biomarker has as yet been validated. However, features such as low levels of epidermal and insulin-like growth factors or uric acid in plasma/ serum and of A beta in CSF, reduction of cerebral cholinergic innervation and metabolism measured by PET mainly in posterior areas, and hippocampal atrophy in MRI might be indicative of distinct deficits with a distinct risk of dementia in subgroups of patients. Longitudinal studies combining the existing techniques and new approaches are needed to identify patients at higher risk of dementia. (C) 2016 International Parkinson and Movement Disorder Society
机译:认知能力下降是帕金森氏病最常见且致残的非运动功能之一。约30%的帕金森氏病患者会出现轻度认知障碍,这是痴呆症发展的公认危险因素。然而,帕金森氏病患者的轻度认知障碍是一个异质性实体,涉及不同类型和程度的认知缺陷。由于目前尚不清楚哪种类型的轻度认知障碍会导致罹患痴呆症的风险更高,因此定义生物标志物以识别这些患者以更好地研究疾病进展和可能的干预措施将非常有用。从这个意义上说,在帕金森氏病和与痴呆症相关的生物标志物的轻度认知障碍患者中进行鉴定将可以尽早发现该过程。这篇综述总结了过去25年的研究,这些研究评估了帕金森氏病患者痴呆症和轻度认知障碍的潜在生物标志物。尽管具有潜在的重要性,但尚未验证任何生物标记。但是,诸如血浆/血清中的表皮和胰岛素样生长因子或尿酸水平低以及脑脊液中的Aβ水平较低,主要在后部通过PET测量的脑胆碱能神经支配和代谢减少以及MRI中的海马萎缩等特征可能可以在患者亚组中显示明显的痴呆和明显的痴呆风险。需要进行纵向研究,将现有技术和新方法结合起来,以鉴定罹患痴呆症较高风险的患者。 (C)2016国际帕金森与运动障碍学会

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