• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

利用静息态功能连接网络的拓扑测度识别阿尔茨海默病的进展阶段:一项比较研究。

Identification of Alzheimer's Disease Progression Stages Using Topological Measures of Resting-State Functional Connectivity Networks: A Comparative Study.

机构信息

School of Electronic Information, Hangzhou Dianzi University, Hangzhou, Zhejiang 310018, China.

School of Computer Science and Technology, Hangzhou Dianzi University, Hangzhou, Zhejiang 310018, China.

出版信息

Behav Neurol. 2022 Jul 4;2022:9958525. doi: 10.1155/2022/9958525. eCollection 2022.

DOI:10.1155/2022/9958525
PMID:35832401
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9273422/
Abstract

Resting-state functional magnetic resonance imaging (rs-fMRI) has been widely employed to examine brain functional connectivity (FC) alterations in various neurological disorders. At present, various computational methods have been proposed to estimate connectivity strength between different brain regions, as the edge weight of FC networks. However, little is known about which model is more sensitive to Alzheimer's disease (AD) progression. This study comparatively characterized topological properties of rs-FC networks constructed with Pearson correlation (PC), dynamic time warping (DTW), and group information guided independent component analysis (GIG-ICA), aimed at investigating the sensitivity and effectivity of these methods in differentiating AD stages. A total of 54 subjects from Alzheimer's Disease Neuroimaging Initiative (ANDI) database, divided into healthy control (HC), mild cognition impairment (MCI), and AD groups, were included in this study. Network-level (global efficiency and characteristic path length) and nodal (clustering coefficient) metrics were used to capture groupwise difference across HC, MCI, and AD groups. The results showed that almost no significant differences were found according to global efficiency and characteristic path length. However, in terms of clustering coefficient, 52 brain parcels sensitive to AD progression were identified in rs-FC networks built with GIG-ICA, much more than PC (6 parcels) and DTW (3 parcels). This indicates that GIG-ICA is more sensitive to AD progression than PC and DTW. The findings also confirmed that the AD-linked FC alterations mostly appeared in temporal, cingulate, and angular areas, which might contribute to clinical diagnosis of AD. Overall, this study provides insights into the topological properties of rs-FC networks over AD progression, suggesting that FC strength estimation of FC networks cannot be neglected in AD-related graph analysis.

摘要

静息态功能磁共振成像(rs-fMRI)已广泛应用于研究各种神经退行性疾病的脑功能连接(FC)改变。目前,已经提出了各种计算方法来估计不同脑区之间的连接强度,作为 FC 网络的边权重。然而,对于哪种模型对阿尔茨海默病(AD)进展更敏感,我们知之甚少。本研究采用 Pearson 相关系数(PC)、动态时间 warping(DTW)和基于组信息引导的独立成分分析(GIG-ICA)构建 rs-FC 网络,比较了它们的拓扑特征,旨在研究这些方法在区分 AD 阶段中的敏感性和有效性。本研究共纳入了来自阿尔茨海默病神经影像学倡议(ADNI)数据库的 54 名受试者,分为健康对照组(HC)、轻度认知障碍组(MCI)和 AD 组。使用网络级(全局效率和特征路径长度)和节点(聚类系数)指标来捕捉 HC、MCI 和 AD 组之间的组间差异。结果表明,根据全局效率和特征路径长度,几乎没有发现显著差异。然而,在聚类系数方面,在基于 GIG-ICA 构建的 rs-FC 网络中,发现了 52 个对 AD 进展敏感的脑区,明显多于 PC(6 个脑区)和 DTW(3 个脑区)。这表明 GIG-ICA 比 PC 和 DTW 更能敏感地检测 AD 进展。研究结果还证实,与 AD 相关的 FC 改变主要出现在颞叶、扣带回和角回等区域,这可能有助于 AD 的临床诊断。总之,本研究深入了解了 rs-FC 网络在 AD 进展过程中的拓扑特征,提示在 AD 相关的图分析中不能忽视 FC 网络的 FC 强度估计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16a0/9273422/3b06264a94e4/BN2022-9958525.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16a0/9273422/216aa6c67fed/BN2022-9958525.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16a0/9273422/e1ff23a259f4/BN2022-9958525.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16a0/9273422/70a7ac0ebc0c/BN2022-9958525.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16a0/9273422/2789bf607e97/BN2022-9958525.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16a0/9273422/3b06264a94e4/BN2022-9958525.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16a0/9273422/216aa6c67fed/BN2022-9958525.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16a0/9273422/e1ff23a259f4/BN2022-9958525.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16a0/9273422/70a7ac0ebc0c/BN2022-9958525.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16a0/9273422/2789bf607e97/BN2022-9958525.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/16a0/9273422/3b06264a94e4/BN2022-9958525.005.jpg

相似文献

1
Identification of Alzheimer's Disease Progression Stages Using Topological Measures of Resting-State Functional Connectivity Networks: A Comparative Study.利用静息态功能连接网络的拓扑测度识别阿尔茨海默病的进展阶段:一项比较研究。
Behav Neurol. 2022 Jul 4;2022:9958525. doi: 10.1155/2022/9958525. eCollection 2022.
2
Quantitative Assessment of Resting-State Functional Connectivity MRI to Differentiate Amnestic Mild Cognitive Impairment, Late-Onset Alzheimer's Disease From Normal Subjects.基于静息态功能连接磁共振成像的定量评估以区分遗忘型轻度认知障碍、晚发型阿尔茨海默病与正常受试者
J Magn Reson Imaging. 2023 Jun;57(6):1702-1712. doi: 10.1002/jmri.28469. Epub 2022 Oct 13.
3
Application of advanced machine learning methods on resting-state fMRI network for identification of mild cognitive impairment and Alzheimer's disease.先进机器学习方法在静息态功能磁共振成像网络上的应用,用于识别轻度认知障碍和阿尔茨海默病。
Brain Imaging Behav. 2016 Sep;10(3):799-817. doi: 10.1007/s11682-015-9448-7.
4
Effects of Brain Parcellation on the Characterization of Topological Deterioration in Alzheimer's Disease.脑分区对阿尔茨海默病拓扑结构退化特征的影响
Front Aging Neurosci. 2019 May 21;11:113. doi: 10.3389/fnagi.2019.00113. eCollection 2019.
5
Does resting state functional connectivity differ between mild cognitive impairment and early Alzheimer's dementia?轻度认知障碍和早期阿尔茨海默病痴呆患者静息态功能连接是否存在差异?
J Neurol Sci. 2020 Nov 15;418:117093. doi: 10.1016/j.jns.2020.117093. Epub 2020 Aug 13.
6
Altered topological organization of high-level visual networks in Alzheimer's disease and mild cognitive impairment patients.阿尔茨海默病和轻度认知障碍患者高级视觉网络的拓扑组织改变。
Neurosci Lett. 2016 Sep 6;630:147-153. doi: 10.1016/j.neulet.2016.07.043. Epub 2016 Jul 25.
7
Decoupling of regional neural activity and inter-regional functional connectivity in Alzheimer's disease: a simultaneous PET/MR study.阿尔茨海默病中区域神经活动与区域间功能连接的解耦:一项同时的 PET/MR 研究。
Eur J Nucl Med Mol Imaging. 2022 Jul;49(9):3173-3185. doi: 10.1007/s00259-022-05692-1. Epub 2022 Feb 24.
8
Alterations of Brain Networks in Alzheimer's Disease and Mild Cognitive Impairment: A Resting State fMRI Study Based on a Population-specific Brain Template.阿尔茨海默病和轻度认知障碍患者脑网络的改变:基于特定人群脑模板的静息态功能磁共振成像研究
Neuroscience. 2021 Jan 1;452:192-207. doi: 10.1016/j.neuroscience.2020.10.023. Epub 2020 Nov 13.
9
A whole-brain computational modeling approach to explain the alterations in resting-state functional connectivity during progression of Alzheimer's disease.一种全脑计算建模方法,用于解释阿尔茨海默病进展过程中静息态功能连接的改变。
Neuroimage Clin. 2017 Aug 8;16:343-354. doi: 10.1016/j.nicl.2017.08.006. eCollection 2017.
10
Interactions Between Aging and Alzheimer's Disease on Structural Brain Networks.衰老与阿尔茨海默病在脑结构网络上的相互作用。
Front Aging Neurosci. 2021 Jun 10;13:639795. doi: 10.3389/fnagi.2021.639795. eCollection 2021.

引用本文的文献

1
Whole-Brain Dynamics Disruptions in the Progression of Alzheimer's Disease: Understanding the Influence of Amyloid-Beta and Tau.阿尔茨海默病进展过程中的全脑动力学紊乱:了解β-淀粉样蛋白和tau蛋白的影响。
bioRxiv. 2024 Mar 31:2024.03.29.587333. doi: 10.1101/2024.03.29.587333.
2
Dynamic multilayer functional connectivity detects preclinical and clinical Alzheimer's disease.动态多层功能连接性可检测临床前和临床期阿尔茨海默病。
Cereb Cortex. 2024 Jan 31;34(2). doi: 10.1093/cercor/bhad542.
3
Correlation transfer function analysis as a biomarker for Alzheimer brain plasticity using longitudinal resting-state fMRI data.

本文引用的文献

1
Towards data-driven group inferences of resting-state fMRI data in rodents: Comparison of group ICA, GIG-ICA, and IVA-GL.迈向啮齿动物静息态功能磁共振成像数据的数据驱动组内推断:组独立成分分析、广义独立成分分析和独立向量分析-广义似然比的比较
J Neurosci Methods. 2022 Jan 15;366:109411. doi: 10.1016/j.jneumeth.2021.109411. Epub 2021 Nov 15.
2
Distinct network topology in Alzheimer's disease and behavioral variant frontotemporal dementia.阿尔茨海默病和行为变异额颞叶痴呆的不同网络拓扑结构。
Alzheimers Res Ther. 2021 Jan 6;13(1):13. doi: 10.1186/s13195-020-00752-w.
3
Communicability Characterization of Structural DWI Subcortical Networks in Alzheimer's Disease.
相关性传递函数分析作为使用纵向静息态 fMRI 数据的阿尔茨海默病大脑可塑性的生物标志物。
Sci Rep. 2023 Dec 6;13(1):21559. doi: 10.1038/s41598-023-48693-2.
阿尔茨海默病中结构性扩散加权成像皮质下网络的传染性特征
Entropy (Basel). 2019 May 6;21(5):475. doi: 10.3390/e21050475.
4
The Dynamics of Functional Brain Networks Associated With Depressive Symptoms in a Nonclinical Sample.非临床样本中与抑郁症状相关的功能性脑网络的动态变化。
Front Neural Circuits. 2020 Sep 18;14:570583. doi: 10.3389/fncir.2020.570583. eCollection 2020.
5
Dynamic time warping outperforms Pearson correlation in detecting atypical functional connectivity in autism spectrum disorders.动态时间规整在检测自闭症谱系障碍中的非典型功能连接方面优于皮尔逊相关系数。
Neuroimage. 2020 Dec;223:117383. doi: 10.1016/j.neuroimage.2020.117383. Epub 2020 Sep 17.
6
Brain States and Transitions: Insights from Computational Neuroscience.脑状态与转变:计算神经科学的新视角。
Cell Rep. 2020 Sep 8;32(10):108128. doi: 10.1016/j.celrep.2020.108128.
7
Functional Connectivity Alterations of the Temporal Lobe and Hippocampus in Semantic Dementia and Alzheimer's Disease.语义性痴呆和阿尔茨海默病中颞叶和海马体的功能连接改变
J Alzheimers Dis. 2020;76(4):1461-1475. doi: 10.3233/JAD-191113.
8
Abnormal dynamic functional network connectivity of the mirror neuron system network and the mentalizing network in patients with adolescent-onset, first-episode, drug-naïve schizophrenia.青少年起病、首发、未用药的精神分裂症患者镜像神经元系统网络和心理化网络的异常动态功能网络连接性
Neurosci Res. 2021 Jan;162:63-70. doi: 10.1016/j.neures.2020.01.003. Epub 2020 Jan 10.
9
A Novel Joint Brain Network Analysis Using Longitudinal Alzheimer's Disease Data.基于纵向阿尔茨海默病数据的新型联合脑网络分析
Sci Rep. 2019 Dec 20;9(1):19589. doi: 10.1038/s41598-019-55818-z.
10
Altered dynamic functional connectivity in weakly-connected state in major depressive disorder.重度抑郁症弱连接状态下动态功能连接的改变。
Clin Neurophysiol. 2019 Nov;130(11):2096-2104. doi: 10.1016/j.clinph.2019.08.009. Epub 2019 Aug 23.