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dc.contributor.authorMaturana Candelas, Aaron 
dc.contributor.authorHornero Sánchez, Roberto 
dc.contributor.authorPoza Crespo, Jesús 
dc.contributor.authorRodríguez González, Víctor 
dc.contributor.authorGutierrez De Pablo, Victor 
dc.contributor.authorPinto, Nádia
dc.contributor.authorRebelo, Miguel Ângelo
dc.contributor.authorGómez Peña, Carlos 
dc.date.accessioned2025-09-30T08:43:29Z
dc.date.available2025-09-30T08:43:29Z
dc.date.issued2025
dc.identifier.citationBiomedical Signal Processing and Control, 2025, vol. 110, p. 108129es
dc.identifier.issn1746-8094es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/78211
dc.descriptionProducción Científicaes
dc.description.abstractThe aim of this study is to examine how variations in the microtubule-associated protein tau (MAPT ) gene affect the brain functional network. For this purpose, resting-state electroencephalogram (EEG) data from 155 participants were acquired. This database included healthy controls and Alzheimer’s disease patients carrying seven MAPT alleles associated with risk or protective effects against neuropathologies or abnormal tau levels. To assess the impact of each genotype on brain function, a multiplex network analysis quantified the connectivity contribution of each brain region across multiple EEG frequency bands (delta, theta, alpha, and beta). To this end, brain functional connectivity was first calculated for each brain region and frequency band using the phase lag index (PLI) parameter. The PLI adjacency matrices in each frequency band corresponded to the layers conforming the multiplex network. Subsequently, the participation coefficient (P) was computed in each brain region to reflect node degree diversification among frequency bands. Carriers of risk and protective alleles exhibited distinct values of P, especially in the left default mode network in healthy controls. In addition, carriers of the risk alleles generally presented higher network disruptions. Finally, significant differences in node degree values were observed across SNPs in the theta and beta frequency bands. These results suggest that different MAPT variants may lead to diverse tau species that influence brain function, particularly in brain regions involved in information flow management in preclinical states. These insights may help understanding network disturbances caused by molecular factors.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherElsevieres
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.classificationAlzheimer’s diseasees
dc.subject.classificationElectroencephalogrames
dc.subject.classificationGeneticses
dc.subject.classificationTaues
dc.subject.classificationBrain connectivityes
dc.subject.classificationMicrotubule-associated protein tau (MAPT )es
dc.titleEffect of MAPT gene variations on the brain electrical activity: A multiplex network studyes
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2025 The Author(s)es
dc.identifier.doi10.1016/j.bspc.2025.108129es
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S1746809425006408es
dc.identifier.publicationfirstpage108129es
dc.identifier.publicationtitleBiomedical Signal Processing and Controles
dc.identifier.publicationvolume110es
dc.peerreviewedSIes
dc.description.projectEsta investigación se ha desarrollado bajo la subvención PGC2018-098214-A-I00 financiada por el Ministerio de Ciencia e Innovación/Agencia Estatal de Investigación/10.13039/501100011033; en el marco del proyecto de I+D+i “Análisis y correlación entre la epigenética y la actividad cerebral para evaluar el riesgo de migraña crónica y episódica en mujeres” (‘Programa de Cooperación Interreg V-A España-Portugal POCTEP 2014-2020’) financiado por la ‘Comisión Europea’ y FEDERes
dc.description.projectMinisterio de Ciencia e Innovación/Agencia Estatal de Investigación/10.13039/501100011033 y por el programa «FEDER: Una manera de hacer Europa» (grant PID2022-138286NB-I00)es
dc.description.projectPortuguese funds through “FCT-Fundação para a Ciência e a Tecnologia”/“Ministério da Ciência, Tecnologia e Inovação” in the framework of the projects ‘Institute for Research and Innovation in Health Sciences’ (POCI-01–0145-FEDER-007274)es
dc.description.projectThe genotyping service was carried out at CEGEN-PRB3-ISCIII; it is supported by grant PT17/0019, of the PE I+D+i 2013–2016, funded by ISCIII and ERDFes
dc.rightsAtribución 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones
dc.subject.unesco32 Ciencias Médicases
dc.subject.unesco33 Ciencias Tecnológicases


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