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阿尔茨海默病和遗忘型轻度认知障碍与 AT(N) 分类和认知失认相关的功能连接差异。

Functional connectivity differences in Alzheimer's disease and amnestic mild cognitive impairment associated with AT(N) classification and anosognosia.

机构信息

University of Groningen, University Medical Center Groningen, Department of Neurology, Groningen, the Netherlands; University of Groningen, University Medical Center Groningen, Alzheimer Center Groningen, Groningen, the Netherlands.

University of Groningen, University Medical Center Groningen, Department of Neurology, Groningen, the Netherlands; University of Groningen, University Medical Center Groningen, Alzheimer Center Groningen, Groningen, the Netherlands.

出版信息

Neurobiol Aging. 2021 May;101:22-39. doi: 10.1016/j.neurobiolaging.2020.12.021. Epub 2021 Jan 8.

Abstract

Alzheimer's continuum biological profiles (ATN, ATN, ATN, and ATN) were established in the 2018 National Institute on Aging and Alzheimer's Association research framework for Alzheimer's disease (AD). We aim to assess the relation between AT(N) biomarker profiles and brain functional connectivity (FC) and assess the neural correlates of anosognosia. We assessed local functional coupling and between-network connectivity through between-group intrinsic local correlation and independent component analyses. The neural correlates of anosognosia were assessed via voxel-wise linear regression analysis in prodromal AD. Statistical significance for the FC analysis was set at p ≤ 0.05 false discovery rate (FDR)-corrected for cluster size. One hundred and twenty-one and 73 participants were included in the FC and the anosognosia analysis, respectively. The FC in the default mode network is greater in prodromal AD than AD with dementia (i.e., local correlation: T = 8.26, p-FDR < 0.001, k = 1179; independent component analysis: cerebellar network, T = 4.01, p-FDR = 0.0012, k = 493). The default mode network is persistently affected in the early stages of Alzheimer's biological continuum. The anterior cingulate cortex (T = 2.52, p-FDR = 0.043, k = 704) is associated with anosognosia in prodromal AD.

摘要

阿尔茨海默病连续体的生物学特征(ATN、ATN、ATN 和 ATN)是在 2018 年美国国家老龄化研究所和阿尔茨海默病协会的阿尔茨海默病研究框架中建立的。我们旨在评估 AT(N)生物标志物特征与大脑功能连接之间的关系,并评估认知失认症的神经相关性。我们通过组间内在局部相关性和独立成分分析评估局部功能耦合和网络间连接。通过对前驱期 AD 进行体素线性回归分析评估认知失认症的神经相关性。FC 分析的统计显著性设定为 p≤0.05 错误发现率(FDR)校正簇大小。分别有 121 名和 73 名参与者纳入 FC 和认知失认症分析。前驱期 AD 中的默认模式网络的功能连接大于痴呆期 AD(即局部相关性:T=8.26,p-FDR<0.001,k=1179;独立成分分析:小脑网络,T=4.01,p-FDR=0.0012,k=493)。默认模式网络在阿尔茨海默病生物连续体的早期阶段持续受到影响。前扣带皮层(T=2.52,p-FDR=0.043,k=704)与前驱期 AD 的认知失认症相关。

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