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对有患阿尔茨海默病风险的未受损个体进行最小生成树分析。

Minimum spanning tree analysis of unimpaired individuals at risk of Alzheimer's disease.

作者信息

García-Colomo Alejandra, López-Sanz David, Stam Cornelis J, Hillebrand Arjan, Carrasco-Gómez Martín, Spuch Carlos, Comis-Tuche María, Maestú Fernando

机构信息

Center for Cognitive and Computational Neuroscience, Complutense University of Madrid, 28223 Pozuelo de Alarcón, Spain.

Department of Experimental Psychology, Cognitive Psychology and Speech and Language Therapy, Complutense University of Madrid, 28223 Pozuelo de Alarcón, Spain.

出版信息

Brain Commun. 2024 Aug 20;6(5):fcae283. doi: 10.1093/braincomms/fcae283. eCollection 2024.

Abstract

Identifying early and non-invasive biomarkers to detect individuals in the earliest stages of the Alzheimer's disease continuum is crucial. As a result, electrophysiology and plasma biomarkers are emerging as great candidates in this pursuit due to their low invasiveness. This is the first magnetoencephalography study to assess the relationship between minimum spanning tree parameters, an alternative to overcome the comparability and thresholding problem issues characteristic of conventional brain network analyses, and plasma phosphorylated tau231 levels in unimpaired individuals, with different risk levels of Alzheimer's disease. Seventy-six individuals with available magnetoencephalography recordings and phosphorylated tau231 plasma determination were included. The minimum spanning tree for the theta, alpha and beta bands for each subject was obtained, and the leaf fraction, tree hierarchy and diameter were calculated. To study the relationship between these topological parameters and phosphorylated tau231, we performed correlation analyses, for the whole sample and considering the two risk sub-groups separately. Increasing concentrations of phosphorylated tau231 were associated with greater leaf fraction and tree hierarchy values, along with lower diameter values, for the alpha and theta frequency bands. These results emerged for the whole sample and the higher risk group, but not for the lower risk group. Our results indicate that the network topology of cognitively unimpaired individuals with elevated plasma phosphorylated tau231 levels, a marker of Alzheimer's disease pathology and amyloid-β accumulation, is already altered, shifting towards a more integrated network increasing its vulnerability and hub-dependency, mostly in the alpha band. This is indicated by increases in leaf fraction and tree hierarchy, along with reductions in diameter. These results match the initial trajectory proposed by theoretical models of disease progression and network disruption and suggest that changes in brain function and organization begin early on.

摘要

识别早期和非侵入性生物标志物以检测处于阿尔茨海默病连续体最早阶段的个体至关重要。因此,由于其低侵入性,电生理学和血浆生物标志物正成为这一研究中的优秀候选对象。这是第一项脑磁图研究,旨在评估最小生成树参数(一种克服传统脑网络分析中可比性和阈值问题的替代方法)与未受损个体中血浆磷酸化tau231水平之间的关系,这些个体具有不同的阿尔茨海默病风险水平。纳入了76名有可用脑磁图记录和磷酸化tau231血浆测定结果的个体。获取了每个受试者θ、α和β频段的最小生成树,并计算了叶分数、树层次和直径。为了研究这些拓扑参数与磷酸化tau231之间的关系,我们对整个样本以及分别考虑两个风险亚组进行了相关性分析。对于α和θ频段,磷酸化tau231浓度的增加与叶分数和树层次值的增加以及直径值的降低相关。这些结果在整个样本和高风险组中出现,但在低风险组中未出现。我们的结果表明,血浆磷酸化tau231水平升高(阿尔茨海默病病理学和淀粉样β蛋白积累的标志物)的认知未受损个体的网络拓扑结构已经改变,向更整合的网络转变,增加了其脆弱性和枢纽依赖性,主要在α频段。这表现为叶分数和树层次的增加以及直径的减小。这些结果与疾病进展和网络破坏的理论模型提出的初始轨迹相符,并表明脑功能和组织的变化在早期就开始了。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c87f/11369931/ebc10157af79/fcae283_ga.jpg

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