载脂蛋白 E4 影响 PHF-Tau 网络的研究

IF 2.7 4区 医学 Q2 CLINICAL NEUROLOGY
Yuan Li, Zhijun Yao, Yongqing Yang, Feng Zhao, Yu Fu, Ying Zou, Bin Hu
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引用次数: 0

摘要

载脂蛋白 E 4 等位基因(APOE 4)是导致轻度认知障碍(MCI)和阿尔茨海默病(AD)的一个重要因素。它在聚集的 Tau 蛋白-配对螺旋丝 Tau(PHF-Tau)的异常修饰中起着主要作用。本研究将143名PHF-Tau PET受试者分为两组(APOE 4携带者和非携带者)。分别计算了两组网络的 PHF-Tau 网络特性和弹性。结果显示,APOE 4 携带者组在所有网络属性上都存在显著差异。我们还发现,APOE 4 携带者在某些脑区的间度中心性存在显著差异。此外,APOE 4 携带者对定向或随机节点故障的恢复能力较弱。我们的研究结果表明,APOE 4 的影响可能导致 PHF-Tau 蛋白网络异常。这些发现对揭示 MCI 患者认知功能障碍的病理生理学可能特别有帮助。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Study on PHF-Tau Network Effected by Apolipoprotein E4.

Apolipoprotein E 4 Allele (APOE 4) is an important factors in Mild cognitive impairment (MCI) and Alzheimer's disease(AD). It plays a primary role in abnormal modification of aggregated Tau protein-paired helical filaments Tau (PHF-Tau). In this study, 143 subjects with PHF-Tau PET were divided into 2 groups (APOE 4 carriers and noncarriers). The measurements of the PHF-Tau network properties and resilient were calculated for 2 group networks respectively. APOE 4 carriers group showed significant differences in all the network properties in the results. We also found significant differences of betweenness centrality in some brain regions for APOE 4 carriers. Moreover, the APOE 4 carriers showed less resilient to targeted or random node failure. Our results indicated that the effects of APOE 4 may lead to abnormalities of PHF-Tau protein network. These findings may be particularly helpful in uncovering the pathophysiology underlying the cognitive dysfunction in MCI patients.

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来源期刊
American Journal of Alzheimers Disease and Other Dementias
American Journal of Alzheimers Disease and Other Dementias GERIATRICS & GERONTOLOGY-CLINICAL NEUROLOGY
CiteScore
5.40
自引率
0.00%
发文量
30
审稿时长
6-12 weeks
期刊介绍: American Journal of Alzheimer''s Disease and other Dementias® (AJADD) is for professionals on the frontlines of Alzheimer''s care, dementia, and clinical depression--especially physicians, nurses, psychiatrists, administrators, and other healthcare specialists who manage patients with dementias and their families. This journal is a member of the Committee on Publication Ethics (COPE).
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