对未受损的阿尔茨海默病风险个体进行最小生成树分析。

IF 4.1 Q1 CLINICAL NEUROLOGY
Brain communications Pub Date : 2024-08-20 eCollection Date: 2024-01-01 DOI:10.1093/braincomms/fcae283
Alejandra García-Colomo, David López-Sanz, Cornelis J Stam, Arjan Hillebrand, Martín Carrasco-Gómez, Carlos Spuch, María Comis-Tuche, Fernando Maestú
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引用次数: 0

摘要

确定早期非侵入性生物标志物,以检测阿尔茨海默病早期阶段的患者至关重要。因此,电生理学和血浆生物标志物因其低侵入性而成为这一目标的最佳候选者。这是首次评估最小生成树参数与血浆磷酸化 tau231 水平之间关系的脑磁图研究,最小生成树参数是克服传统脑网络分析所特有的可比性和阈值问题的替代方法,而血浆磷酸化 tau231 水平则是针对不同阿尔茨海默病风险水平的未受损个体。研究对象包括 76 名有脑磁图记录和血浆磷酸化 tau231 测定结果的人。研究人员获得了每个受试者θ、α和β波段的最小生成树,并计算了树叶比例、树的层次结构和直径。为了研究这些拓扑参数与磷酸化 tau231 之间的关系,我们对整个样本和两个风险亚组分别进行了相关性分析。在α和θ频带,磷酸化tau231浓度的增加与更高的叶片比例和树木等级值以及更低的直径值相关。这些结果出现在整个样本和高风险组中,但不出现在低风险组中。我们的研究结果表明,血浆磷酸化 tau231(阿尔茨海默病病理和淀粉样蛋白-β积累的标志物)水平升高的认知功能未受损个体的网络拓扑结构已经发生了改变,主要在 alpha 频段,其网络转向更加综合的网络,增加了网络的脆弱性和枢纽依赖性。叶片比例和树的层次结构的增加以及直径的减小都表明了这一点。这些结果与疾病进展和网络破坏理论模型提出的初始轨迹相吻合,表明大脑功能和组织的变化很早就开始了。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Minimum spanning tree analysis of unimpaired individuals at risk of Alzheimer's disease.

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.

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CiteScore
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