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dc.contributor.authorCantero, José L.es_ES
dc.contributor.authorAtienza, Mercedeses_ES
dc.contributor.authorSánchez-Juan, Pascual es_ES
dc.contributor.authorRodríguez Rodríguez, Eloy Manuel es_ES
dc.contributor.authorVázquez Higuera, José Luises_ES
dc.contributor.authorPozueta Cantudo, Anaes_ES
dc.contributor.authorGonzález Suárez, Andreaes_ES
dc.contributor.authorVilaplana, Eduardes_ES
dc.contributor.authorPegueroles, Jordies_ES
dc.contributor.authorMontal, Víctores_ES
dc.contributor.authorBlesa, Rafaeles_ES
dc.contributor.authorAlcolea, Danieles_ES
dc.contributor.authorLleo, Albertoes_ES
dc.contributor.authorFortea, Juanes_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2018-01-24T17:05:14Z
dc.date.available2019-04-01T02:45:09Z
dc.date.issued2018-04es_ES
dc.identifier.issn0197-4580es_ES
dc.identifier.issn1558-1497es_ES
dc.identifier.otherSAF2011-25463es_ES
dc.identifier.otherPSI2014-55747-Res_ES
dc.identifier.urihttp://hdl.handle.net/10902/12928
dc.description.abstractThe diagnostic value of cerebrospinal fluid (CSF) biomarkers is well established in Alzheimer's disease, but our current knowledge about how abnormal CSF levels affect cerebral integrity, at local and network levels, is incomplete in asymptomatic older adults. Here, we have collected CSF samples and performed structural magnetic resonance imaging scans in cognitively normal elderly as part of a cross-sectional multicenter study (SIGNAL project). To identify group differences in cortical thickness, white matter volume, and properties of structural networks, participants were split into controls (N = 20), positive amyloid-? (A?1?42 +) (N = 19), and positive phosphorylated tau (N = 18). The A?1?42 + group exhibited thickening of middle temporal regions, while positive phosphorylated tau individuals showed thinning in the superior parietal and orbitofrontal cortices. Subjects with abnormal CSF biomarkers further showed regional white matter atrophy and more segregated cortical networks, the A?1?42 + group showing heightened isolation of cingulate and temporal cortices. Collectively, these findings highlight the relevance of combining structural brain imaging and connectomics for in vivo tracking of Alzheimer's disease lesions in asymptomatic stages.es_ES
dc.description.sponsorshipThis work was supported by research grants from the Spanish Ministry of Economy and Competitiveness (SAF2011-25463 to J.L.C., PSI2014-55747-R to M.A.), the Carlos III Institute of Health, Spain (PI11/02425 and PI14/01126 to J.F.; PI11/3035 and PI14/1561 to A.L.; PI08/0139, PI12/02288 and PI16/01652 to P.S.J.), jointly funded by Fondo Europeo de Desarrollo Regional (FEDER), Unión Europea, “Una manera de hacer Europa”, the Joint Programming in Neurodegenerative Disease Research (DEMTEST to P.S.J.), “Marató TV3” (project 20141210 to J.F. and 20142610 to A.L.), the Regional Ministry of Innovation, Science and Enterprise, Junta de Andalucia (P12- CTS-2327 to J.C.L.), and the CIBERNED program (Signal project).es_ES
dc.format.extent9 p.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rights© <2018> Elsevier. This manuscript version is made available under the CC-BY-NC-ND 4.0 licensees_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceNeurobiology of Aging Volume 64, April 2018, Pages 58-67es_ES
dc.subject.otherPreclinical Alzheimer's diseasees_ES
dc.subject.otherSNAPes_ES
dc.subject.otherCSF biomarkerses_ES
dc.subject.otherCortical thicknesses_ES
dc.subject.otherStructural cortical networkses_ES
dc.subject.otherWhite matteres_ES
dc.titleCerebral changes and disrupted gray-matter cortical networks in asymptomatic older adults at risk for Alzheimer's diseasees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.neurobiolaging.2017.12.010es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.neurobiolaging.2017.12.010es_ES
dc.type.versionacceptedVersiones_ES


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© <2018> Elsevier. This manuscript version is made available under the CC-BY-NC-ND 4.0 licenseExcepto si se señala otra cosa, la licencia del ítem se describe como © <2018> Elsevier. This manuscript version is made available under the CC-BY-NC-ND 4.0 license