Evidence map›Paper›PMID 42153007›Full record

ArticleBiomedical engineering and computational biology2026

Blind Identification of Altered Functional Subnetworks in Alzheimer's Disease Using Resting-State fMRI.

Farzaneh Keyvanfard, Abbas Nasiraei-Moghaddam

Abstract read
In one paragraph

Article in Biomedical engineering and computational biology, 2026. 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Farzaneh KeyvanfardDepartment of Biomedical Engineering, Faculty of Electrical Engineering, K. N. Toosi University of Technology, Tehran, Iran.ORCID https://orcid.org/0000-0001-8516-5709
Abbas Nasiraei-MoghaddamDepartment of Biomedical Engineering, Amirkabir University of Technology (Tehran Polytechnic), Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Resting-state functional magnetic resonance imaging (rs-fMRI) is widely used to examine functional connectivity (FC) alterations in neurological disorders such as Alzheimer's disease (AD). Traditional studies either employ whole-brain analyses or focus on specific regions, yet the vast number of FCs and their interrelations complicate interpretation. This study adopts a data-driven, hypothesis-free approach to detect altered functional subnetworks in AD. Methods: Independent component analysis (ICA) was applied to FC matrices from 34 AD patients and 49 healthy controls (HCs) from the Alzheimer's Disease Neuroimaging Initiative (ADNI). After pruning, significant subnetworks distinguishing AD from HC were identified. Graph theoretical parameters were computed for each subnetwork, and their associations with Mini-Mental State Examination (MMSE) scores were assessed. Results: Three subnetworks effectively differentiated AD patients from HCs. One subnetwork showed significant group differences in network strength, clustering coefficient, and local efficiency, despite no whole-brain differences. Abnormal functional lateralization also emerged within subnetworks. Moreover, FC weights in the identified subnetworks positively correlated with MMSE scores, linking cognitive performance to subnetwork connectivity. Conclusion: These results demonstrate the utility of a data-driven approach in detecting AD-specific altered subnetworks. By providing a modular perspective, this method facilitates targeted examination of connectivity changes, improves interpretability, and deepens understanding of functional disruptions in AD.

Indexed as

Alzheimerblind analysisbrain subnetworkfunctional connectivityrs-fMRI

Identifiers

PMID42153007
PMCPMC13180186

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.