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帕金森病中痴呆和轻度认知障碍的生物标志物。

Biomarkers for dementia and mild cognitive impairment in Parkinson's disease.

作者信息

Delgado-Alvarado Manuel, Gago Belén, Navalpotro-Gomez Irene, Jiménez-Urbieta Haritz, Rodriguez-Oroz María C

机构信息

Biodonostia Health Research Institute, San Sebastián, Spain.

Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain.

出版信息

Mov Disord. 2016 Jun;31(6):861-81. doi: 10.1002/mds.26662. Epub 2016 May 19.

Abstract

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 Aß 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. © 2016 International Parkinson and Movement Disorder Society.

摘要

认知功能衰退是帕金森病最常见且致残的非运动症状之一。约30%的帕金森病患者会出现轻度认知障碍,这是痴呆发生的一个公认风险因素。然而,帕金森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使发展为痴呆的风险更高,因此定义能够识别这些患者的生物标志物,以更好地研究疾病进展和可能的干预措施将很有帮助。从这个意义上讲,在帕金森病和轻度认知障碍患者中识别与痴呆相关的生物标志物将有助于早期发现这一过程。本综述总结了过去25年中评估帕金森病患者痴呆和轻度认知障碍潜在生物标志物的研究。尽管具有潜在重要性,但尚无生物标志物得到验证。然而,血浆/血清中表皮生长因子、胰岛素样生长因子或尿酸水平低,脑脊液中Aβ水平低,PET主要在后脑区域测量的脑胆碱能神经支配和代谢降低,以及MRI显示的海马萎缩等特征,可能表明患者亚组中存在不同的缺陷以及不同的痴呆风险。需要结合现有技术和新方法的纵向研究来识别痴呆风险较高的患者。© 2016国际帕金森病和运动障碍协会

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