TgF344-AD 阿尔茨海默病大鼠模型缺省模式样网络中的节点度中心性作为早期网络改变的衡量标准。

IF 4.1 Q2 GERIATRICS & GERONTOLOGY npj aging Pub Date : 2024-06-20 DOI:10.1038/s41514-024-00151-7
Saba Amiri, Monica van den Berg, Mohammad-Reza Nazem-Zadeh, Marleen Verhoye, Mahmood Amiri, Georgios A Keliris
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摘要

本研究调查了阿尔茨海默病(AD)大鼠模型在疾病进展早期阶段缺省模式样网络(DMLN)的脑网络改变,并将其应用于开发AD早期诊断生物标记物的转化研究。13只雄性TgF344-AD(TG)大鼠和11只雄性野生型(WT)小鼠分别在4个月和6个月大(AD的前期和早期斑块阶段)时接受了纵向静息态fMRI检查。通过计算节点度(ND)来描述DMLN内部连通性的改变,节点度是一种图论的中心性度量。研究发现,与年龄匹配的WT同窝鼠相比,4个月大的TG组群海马左侧CA2亚区的ND值明显较低。此外,在 6 个月大的 TG 组群中,与同龄的 WT 组群相比,右侧边缘前皮层(prL)和基底前脑的 ND 值更低(低连接性)。事实上,TG 和 WT 队列中 DMLN 的 ND 模式在代表疾病进展的斑块前和早期斑块阶段的两个时间点上都有显著差异。我们的研究结果表明,与健康对照组相比,AD斑块前期左侧CA2中较低的结节度(低连接性)和斑块早期基底前脑与DMLN区域之间的低连接性表现出差异。这些结果表明,节点度这种图论测量方法可以描述大脑网络的特征,并提高我们对阿尔茨海默病发病机制的洞察力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Nodal degree centrality in the default mode-like network of the TgF344-AD Alzheimer's disease rat model as a measure of early network alterations.

This study investigates brain network alterations in the default mode-like network (DMLN) at early stages of disease progression in a rat model of Alzheimer's disease (AD) with application in the development of early diagnostic biomarkers of AD in translational studies. Thirteen male TgF344-AD (TG) rats, and eleven male wild-types (WT) littermates underwent longitudinal resting-state fMRI at the age of 4 and 6 months (pre and early-plaque stages of AD). Alterations in connectivity within DMLN were characterized by calculating the nodal degree (ND), a graph theoretical measure of centrality. The ND values of the left CA2 subregion of the hippocampus was found to be significantly lower in the 4-month-old TG cohort compared to the age-matched WT littermates. Moreover, a lower ND value (hypo-connectivity) was observed in the right prelimbic cortex (prL) and basal forebrain in the 6-month-old TG cohort, compared to the same age WT cohort. Indeed, the ND pattern in the DMLN in both TG and WT cohorts showed significant differences across the two time points that represent pre-plaque and early plaque stages of disease progression. Our findings indicate that lower nodal degree (hypo-connectivity) in the left CA2 in the pre-plaque stage of AD and hypo-connectivity between the basal forebrain and the DMLN regions in the early-plaque stage demonstrated differences in comparison to healthy controls. These results suggest that a graph-theoretical measure such as the nodal degree, can characterize brain networks and improve our insights into the mechanisms underlying Alzheimer's disease.

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