Primate brain pattern-based automated Alzheimer's disease detection model using EEG signals

dc.contributor.authorDogan, Sengul
dc.contributor.authorBaygin, Mehmet
dc.contributor.authorTasci, Burak
dc.contributor.authorLoh, Hui Wen
dc.contributor.authorBarua, Prabal D.
dc.contributor.authorTuncer, Turker
dc.contributor.authorAcharya, U. Rajendra
dc.date.accessioned2026-08-12T17:36:55Z
dc.date.issued2023
dc.departmentFırat Üniversitesi
dc.description.abstractElectroencephalography (EEG) may detect early changes in Alzheimer's disease (AD), a debilitating progressive neurodegenerative disease. We have developed an automated AD detection model using a novel directed graph for local texture feature extraction with EEG signals. The proposed graph was created from a topological map of the macroscopic connectome, i.e., neuronal pathways linking anatomo-functional brain segments involved in visual object recognition and motor response in the primate brain. This primate brain pattern (PBP)-based model was tested on a public AD EEG signal dataset. The dataset comprised 16-channel EEG signal recordings of 12 AD patients and 11 healthy controls. While PBP could generate 448 low-level features per one-dimensional EEG signal, combining it with tunable q-factor wavelet transform created a multilevel feature extractor (which mimicked deep models) to generate 8,512 (= 448 x 19) features per signal input. Iterative neighborhood component analysis was used to choose the most discriminative features (the number of optimal features varied among the individual EEG channels) to feed to a weighted k-nearest neighbor (KNN) classifier for binary classification into AD vs. healthy using both leave-one subject-out (LOSO) and tenfold cross-validations. Iterative majority voting was used to compute subject-level general performance results from the individual channel classification outputs. Channel-wise, as well as subject-level general results demonstrated exemplary performance. In addition, the model attained 100% and 92.01% accuracy for AD vs. healthy classification using the KNN classifier with tenfold and LOSO cross-validations, respectively. Our developed multilevel PBP-based model extracted discriminative features from EEG signals and paved the way for further development of models inspired by the brain connectome.
dc.identifier.doi10.1007/s11571-022-09859-2
dc.identifier.endpage659
dc.identifier.issn1871-4080
dc.identifier.issn1871-4099
dc.identifier.issue3
dc.identifier.orcid0000-0001-6449-8950
dc.identifier.orcid0000-0001-9677-5684
dc.identifier.orcid0000-0002-4490-0946
dc.identifier.orcid0000-0003-2689-8552
dc.identifier.pmid37265658
dc.identifier.scopus2-s2.0-85135810314
dc.identifier.scopusqualityQ1
dc.identifier.startpage647
dc.identifier.urihttps://doi.org/10.1007/s11571-022-09859-2
dc.identifier.urihttps://hdl.handle.net/11508/58120
dc.identifier.volume17
dc.identifier.wosWOS:000839538800001
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherSpringer
dc.relation.ispartofCognitive Neurodynamics
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectPrimate brain modelling
dc.subjectFeature engineering
dc.subjectEEG signal classification
dc.subjectFeature extraction
dc.subjectAD detection
dc.titlePrimate brain pattern-based automated Alzheimer's disease detection model using EEG signals
dc.typeArticle

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