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Complexity Analysis of the Default Mode Network Using Resting-State fMRI in Down Syndrome: Relationships Highlighted by A Neuropsychological Assessment

dc.contributor.authorFigueroa Jiménez, María Dolores
dc.contributor.authorCarbó-Carreté, Maria
dc.contributor.authorCañete-Massé, Cristina
dc.contributor.authorZarabozo-Hurtado, Daniel
dc.contributor.authorPeró, Maribel
dc.contributor.authorSalazar Estrada, José Guadalupe
dc.contributor.authorGuàrdia-Olmos, Joan, 1958-
dc.date.accessioned2021-03-05T10:04:39Z
dc.date.available2021-03-05T10:04:39Z
dc.date.issued2021-03-02
dc.date.updated2021-03-05T10:04:39Z
dc.description.abstractBackground: Studies on complexity indicators in the field of functional connectivity derived from resting-state fMRI (rs-fMRI) in Down syndrome (DS) samples and their possible relationship with cognitive functioning variables are rare. We analyze how some complexity indicators estimated in the subareas that constitute the default mode network (DMN) might be predictors of the neuropsychological outcomes evaluating Intelligence Quotient (IQ) and cognitive performance in persons with DS. Methods: Twenty-two DS people were assessed with the Kaufman Brief Test of Intelligence (KBIT) and Frontal Assessment Battery (FAB) tests, and fMRI signals were recorded in a resting state over a six-minute period. In addition, 22 controls, matched by age and sex, were evaluated with the same rs-fMRI procedure. Results: There was a significant difference in complexity indicators between groups: the control group showed less complexity than the DS group. Moreover, the DS group showed more variance in the complexity indicator distributions than the control group. In the DS group, significant and negative relationships were found between some of the complexity indicators in some of the DMN networks and the cognitive performance scores. Conclusions: The DS group is characterized by more complex DMN networks and exhibits an inverse relationship between complexity and cognitive performance based on the negative parameter estimates.
dc.format.extent19 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec707510
dc.identifier.issn2076-3425
dc.identifier.pmid33801471
dc.identifier.urihttps://hdl.handle.net/2445/174684
dc.language.isoeng
dc.publisherMDPI
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3390/brainsci11030311
dc.relation.ispartofBrain Sciences, 2021, vol. 11, num. 3, p. 311
dc.relation.urihttps://doi.org/10.3390/brainsci11030311
dc.rightscc-by (c) Figueroa Jimenez, María Dolores et al., 2021
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Psicologia Social i Psicologia Quantitativa)
dc.subject.classificationSíndrome de Down
dc.subject.classificationImatges per ressonància magnètica
dc.subject.classificationNeuropsicologia
dc.subject.otherDown syndrome
dc.subject.otherMagnetic resonance imaging
dc.subject.otherNeuropsychology
dc.titleComplexity Analysis of the Default Mode Network Using Resting-State fMRI in Down Syndrome: Relationships Highlighted by A Neuropsychological Assessment
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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