dc.contributor.author | Maturana Candelas, Aaron | |
dc.contributor.author | Hornero Sánchez, Roberto | |
dc.contributor.author | Poza Crespo, Jesús | |
dc.contributor.author | Rodríguez González, Víctor | |
dc.contributor.author | Gutierrez De Pablo, Victor | |
dc.contributor.author | Pinto, Nádia | |
dc.contributor.author | Rebelo, Miguel Ângelo | |
dc.contributor.author | Gómez Peña, Carlos | |
dc.date.accessioned | 2025-09-30T08:43:29Z | |
dc.date.available | 2025-09-30T08:43:29Z | |
dc.date.issued | 2025 | |
dc.identifier.citation | Biomedical Signal Processing and Control, 2025, vol. 110, p. 108129 | es |
dc.identifier.issn | 1746-8094 | es |
dc.identifier.uri | https://uvadoc.uva.es/handle/10324/78211 | |
dc.description | Producción Científica | es |
dc.description.abstract | The 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.mimetype | application/pdf | es |
dc.language.iso | eng | es |
dc.publisher | Elsevier | es |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | es |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.subject.classification | Alzheimer’s disease | es |
dc.subject.classification | Electroencephalogram | es |
dc.subject.classification | Genetics | es |
dc.subject.classification | Tau | es |
dc.subject.classification | Brain connectivity | es |
dc.subject.classification | Microtubule-associated protein tau (MAPT ) | es |
dc.title | Effect of MAPT gene variations on the brain electrical activity: A multiplex network study | es |
dc.type | info:eu-repo/semantics/article | es |
dc.rights.holder | © 2025 The Author(s) | es |
dc.identifier.doi | 10.1016/j.bspc.2025.108129 | es |
dc.relation.publisherversion | https://www.sciencedirect.com/science/article/pii/S1746809425006408 | es |
dc.identifier.publicationfirstpage | 108129 | es |
dc.identifier.publicationtitle | Biomedical Signal Processing and Control | es |
dc.identifier.publicationvolume | 110 | es |
dc.peerreviewed | SI | es |
dc.description.project | Esta 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 FEDER | es |
dc.description.project | Ministerio 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.project | Portuguese 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.project | The 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 ERDF | es |
dc.rights | Atribución 4.0 Internacional | * |
dc.type.hasVersion | info:eu-repo/semantics/publishedVersion | es |
dc.subject.unesco | 32 Ciencias Médicas | es |
dc.subject.unesco | 33 Ciencias Tecnológicas | es |