Multiway array decomposition analysis of EEGs in Alzheimer's disease

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dc.contributor.authorLatchoumane, Charles-Francois V.ko
dc.contributor.authorVialatte, Francois-Benoisko
dc.contributor.authorSole-Casals, Jordiko
dc.contributor.authorMaurice, Moniqueko
dc.contributor.authorWimalaratna, Sunil R.ko
dc.contributor.authorHudson, Nigelko
dc.contributor.authorJeong, Jaeseungko
dc.contributor.authorCichocki, Andrzejko
dc.date.accessioned2013-03-12T15:09:13Z-
dc.date.available2013-03-12T15:09:13Z-
dc.date.created2012-06-29-
dc.date.created2012-06-29-
dc.date.issued2012-05-
dc.identifier.citationJOURNAL OF NEUROSCIENCE METHODS, v.207, no.1, pp.41 - 50-
dc.identifier.issn0165-0270-
dc.identifier.urihttp://hdl.handle.net/10203/102671-
dc.description.abstractMethods for the extraction of features from physiological datasets are growing needs as clinical investigations of Alzheimer's disease (AD) in large and heterogeneous population increase. General tools allowing diagnostic regardless of recording sites, such as different: hospitals, are essential and if combined to inexpensive non-invasive methods could critically improve mass screening of subjects with AD. In this study, we applied two state of the art multiway array decomposition (MAD) methods to extract unique features from electroencephalograms (EEGs) of AD patients obtained from multiple sites. In comparison to MAD, spectral-spatial average filter (SSFs) of control and AD subjects were used as well as a common blind source separation method, algorithm for multiple unknown signal extraction (AMUSE), and singular value decomposition (SVD) coupled to tensor unfolding. We trained a feed-forward multilayer perceptron (MLP) to validate and optimize AD classification from two independent databases. Using a third EEG dataset, we demonstrated that features extracted from MAD outperformed features obtained from SSFs AMUSE in terms of root mean squared error (RMSE) and reaching up to 100% of accuracy in test condition. We propose that MAD maybe a useful tool to extract features for AD diagnosis offering great generalization across multi-site databases and opening doors to the discovery of new characterization of the disease. (C) 2012 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE BV-
dc.subjectMILD COGNITIVE IMPAIRMENT-
dc.subjectHIPPOCAMPAL ATROPHY-
dc.subjectQUANTITATIVE EEG-
dc.subjectSENILE DEMENTIA-
dc.subjectCLASSIFICATION-
dc.subjectFREQUENCY-
dc.subjectCOHERENCE-
dc.subjectSTATE-
dc.subjectDISCRIMINATION-
dc.subjectPROGRESSION-
dc.titleMultiway array decomposition analysis of EEGs in Alzheimer's disease-
dc.typeArticle-
dc.identifier.wosid000304511400005-
dc.identifier.scopusid2-s2.0-84859716657-
dc.type.rimsART-
dc.citation.volume207-
dc.citation.issue1-
dc.citation.beginningpage41-
dc.citation.endingpage50-
dc.citation.publicationnameJOURNAL OF NEUROSCIENCE METHODS-
dc.identifier.doi10.1016/j.jneumeth.2012.03.005-
dc.contributor.localauthorJeong, Jaeseung-
dc.contributor.nonIdAuthorVialatte, Francois-Benois-
dc.contributor.nonIdAuthorSole-Casals, Jordi-
dc.contributor.nonIdAuthorMaurice, Monique-
dc.contributor.nonIdAuthorWimalaratna, Sunil R.-
dc.contributor.nonIdAuthorHudson, Nigel-
dc.contributor.nonIdAuthorCichocki, Andrzej-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorAlzheimer&apos-
dc.subject.keywordAuthors disease-
dc.subject.keywordAuthorEEC-
dc.subject.keywordAuthorDiagnosis-
dc.subject.keywordAuthorMultiway array decomposition-
dc.subject.keywordAuthorPARAFAC-
dc.subject.keywordAuthorNTD-
dc.subject.keywordPlusMILD COGNITIVE IMPAIRMENT-
dc.subject.keywordPlusHIPPOCAMPAL ATROPHY-
dc.subject.keywordPlusQUANTITATIVE EEG-
dc.subject.keywordPlusSENILE DEMENTIA-
dc.subject.keywordPlusCLASSIFICATION-
dc.subject.keywordPlusFREQUENCY-
dc.subject.keywordPlusCOHERENCE-
dc.subject.keywordPlusSTATE-
dc.subject.keywordPlusDISCRIMINATION-
dc.subject.keywordPlusPROGRESSION-
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