Evidence map›Paper›PMID 40537925›Full record

ArticleCNS neuroscience & therapeutics2025

Network Topography Alterations in Alzheimer's Disease: Insights From Motif Changes via Multisite Datasets (N = 3262).

Juntao Zhao, Yunyun Duan, Kun Zhao, Hongwei Li, Dawei Wang, Hongxiang Yao, Bo Zhou, Jie Lu, Pan Wang, Yan Chen and 4 more

Abstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Juntao ZhaoSchool of Artificial Intelligence, Beijing University of Posts and Telecommunications, Beijing, China.
Yunyun DuanDepartment of Radiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
Kun ZhaoSchool of Artificial Intelligence, Beijing University of Posts and Telecommunications, Beijing, China.ORCID 0000-0002-5196-100X
Hongwei LiSchool of Artificial Intelligence, Beijing University of Posts and Telecommunications, Beijing, China.
Dawei WangDepartment of Radiology, Qilu Hospital of Shandong University, Jinan, China.ORCID 0000-0002-4488-2135
Hongxiang YaoDepartment of Radiology, The Second Medical Centre, National Clinical Research Centre for Geriatric Diseases, Chinese PLA General Hospital, Beijing, China.
Bo ZhouDepartment of Neurology, The Second Medical Centre, National Clinical Research Centre for Geriatric Diseases, Chinese PLA General Hospital, Beijing, China.
Jie LuDepartment of Radiology, Xuanwu Hospital of Capital Medical University, Beijing, China.ORCID 0000-0003-0425-3921
Pan WangDepartment of Neurology, Tianjin Huanhu Hospital, Tianjin, China.
Yan ChenDepartment of Psychiatry, People's Hospital of Hangzhou Medical College, Zhejiang Provincial People's Hospital, Hangzhou, China.
Xi ZhangDepartment of Neurology, The Second Medical Centre, National Clinical Research Centre for Geriatric Diseases, Chinese PLA General Hospital, Beijing, China.
Ying HanDepartment of Neurology, Xuanwu Hospital of Capital Medical University, Beijing, China.ORCID 0000-0003-0377-7424
Yong LiuSchool of Artificial Intelligence, Beijing University of Posts and Telecommunications, Beijing, China.ORCID 0000-0002-1862-3121
Zhengluan LiaoDepartment of Psychiatry, People's Hospital of Hangzhou Medical College, Zhejiang Provincial People's Hospital, Hangzhou, China.

Funding

Beijing Municipal Natural Science Foundation 7244519National Natural Science Foundation of China 62333002National Natural Science Foundation of China 82172018National Natural Science Foundation of China 82401858National Natural Science Foundation of China T2425027
6 · The paper itself

Abstract

backgroundConvergent studies have demonstrated that the topological structure of the brain network undergoes significant alterations in Alzheimer's Disease (AD). However, the underlying mechanisms driving these topological changes remain unclear. Network motifs, as fundamental components of brain networks, provide valuable insights into how disconnections may lead to alterations in the macroscale topological structure.

methodsThis study focuses on undirected triangle motifs within the brain network, identifying 20 unique undirected triangle motifs based on edge strength and length derived from the regional radiomics similarity network (R2SN). To comprehensively capture the distribution of these motifs, we introduce a measure named Principal Motif Value (PMV) of the 20 motifs using principal component analysis (PCA).

resultsOur findings reveal significant spatial heterogeneity in PMV across different brain regions. In addition, we identify reproducible alterations of PMV in AD, which were observed through three independent datasets, particularly in the inferior temporal gyrus, middle temporal gyrus, and parahippocampal gyrus. Notably, PMV demonstrates significant correlations with clinical manifestations and neurological features. Finally, we elucidate that alterations in PMV are associated with gene expression related to neuronal systems and synapsis features.

conclusionThese findings provide novel insights into the relationship between disconnection and the topological structure of the brain network in AD.

Indexed as

Alzheimer DiseaseBrainNerve NetAgedAged, 80 and overDatabases, FactualFemaleHumansMagnetic Resonance ImagingMaleNeural PathwaysAlzheimer's diseasebrain networkmotifregional radiomics similarity network

Identifiers

PMID40537925
PMCPMC12178941

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