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神经退行性疾病中的胆碱能功能障碍、神经退行性变和淀粉样β病理学。

Cholinergic dysfunction, neurodegeneration, and amyloid-beta pathology in neurodegenerative diseases.

机构信息

Division of Clinical Geriatrics, Center for Alzheimer Research, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.

Geriatric Clinic, Landspitali University Hospital Landakot, Reykjavik, Iceland.

出版信息

Psychiatry Res Neuroimaging. 2020 Aug 30;302:111099. doi: 10.1016/j.pscychresns.2020.111099. Epub 2020 May 17.

DOI:10.1016/j.pscychresns.2020.111099
PMID:32505903
Abstract

Cholinergic dysfunction is central in Alzheimer's disease (AD) and dementia with Lewy bodies (DLB). The electroencephalography-based acetylcholine index (EEG-Ach index) has been proposed as a biomarker of cholinergic dysfunction. However, it is unclear how the EEG-Ach index relates to amyloid-beta pathology and neurodegeneration. We investigated the association between the EEG-Ach index and cerebrospinal fluid (CSF) amyloid-beta, CSF total tau, cortical thickness, and hippocampal volume from magnetic resonance imaging (MRI), and cognition. A total of 127 patients with different neurodegenerative diseases were studied. The EEG-Ach index was calculated from quantitative EEG using statistical pattern recognition. The EEG-Ach index was associated with hippocampal volume and cortical thickness in frontal, temporal, and occipital cortices. Cross-sectional sub-analyses based on a small sample suggests that the EEG-Ach index increases the closest to AD dementia, downstream to amyloid-beta pathology, CSF total tau, and hippocampal volume. We conclude that cholinergic dysfunction correlates with atrophy in brain areas important for AD pathogenesis, and this association is more prominent in the dementia stage. These results together with previous studies from this project suggest that the EEG-Ach index may be a useful biomarker for cholinergic dysfunction, with value for differential diagnosis of dementia and monitoring patients at the dementia stage.

摘要

胆碱能功能障碍是阿尔茨海默病(AD)和路易体痴呆(DLB)的核心。基于脑电图的乙酰胆碱指数(EEG-Ach 指数)已被提议作为胆碱能功能障碍的生物标志物。然而,目前尚不清楚 EEG-Ach 指数与淀粉样蛋白-β病理学和神经退行性变之间的关系。我们研究了 EEG-Ach 指数与脑脊液(CSF)淀粉样蛋白-β、CSF 总tau、皮质厚度和磁共振成像(MRI)海马体积以及认知之间的关系。共研究了 127 名患有不同神经退行性疾病的患者。EEG-Ach 指数是通过使用统计模式识别的定量 EEG 计算得出的。EEG-Ach 指数与额叶、颞叶和枕叶皮质的海马体积和皮质厚度相关。基于小样本的横截面亚分析表明,EEG-Ach 指数增加最接近 AD 痴呆,下游与淀粉样蛋白-β病理学、CSF 总 tau 和海马体积相关。我们得出结论,胆碱能功能障碍与 AD 发病机制相关脑区的萎缩相关,这种关联在痴呆阶段更为明显。这些结果与该项目的先前研究一起表明,EEG-Ach 指数可能是胆碱能功能障碍的有用生物标志物,对痴呆症的鉴别诊断和痴呆症阶段患者的监测具有价值。

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