Brain atrophy and clinical characterization of adults with mild cognitive impairment and different cerebrospinal fluid biomarker profiles according to the AT(N) research framework of Alzheimer’s disease

dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Psicoloxía Clínica e Psicobioloxíagl
dc.contributor.affiliationUniversidade de Santiago de Compostela. Departamento de Psicoloxía Evolutiva e da Educacióngl
dc.contributor.authorRivas Fernández, Miguel Ángel
dc.contributor.authorLindín, Mónica
dc.contributor.authorZurrón Ocio, Montserrat
dc.contributor.authorDíaz Fernández, Fernando
dc.contributor.authorAldrey Vázquez, José Manuel
dc.contributor.authorPías Peleteiro, Juan Manuel
dc.contributor.authorVázquez-Vázquez, Laura
dc.contributor.authorPereiro Rozas, Arturo X.
dc.contributor.authorLojo Seoane, Cristina
dc.contributor.authorNieto Vieites, Ana
dc.contributor.authorGaldo Álvarez, Santiago
dc.date.accessioned2023-01-23T10:12:31Z
dc.date.available2023-01-23T10:12:31Z
dc.date.issued2022
dc.description.abstractIntroduction: This study aimed to evaluate, in adults with mild cognitive impairment (MCI), the brain atrophy that may distinguish between three AT(N) biomarker-based profiles, and to determine its clinical value. Methods: Structural MRI (sMRI) was employed to evaluate the volume and cortical thickness differences in MCI patients with different AT(N) profiles, namely, A−T−(N)−: normal AD biomarkers; A+T−(N)−: AD pathologic change; and A+T+(N)+: prodromal AD. Sensitivity and specificity of these changes were also estimated. Results: An initial atrophy in medial temporal lobe (MTL) areas was found in the A+T−(N)− and A+T+(N)+ groups, spreading toward the parietal and frontal regions in A+T+(N)+ patients. These structural changes allowed distinguishing AT(N) profiles within the AD continuum; however, the profiles and their pattern of neurodegeneration were unsuccessful to determine the current clinical status. Conclusion: sMRI is useful in the determination of the specific brain structural changes of AT(N) profiles along the AD continuum, allowing differentiation between MCI adults with or without pathological AD biomarkersgl
dc.description.peerreviewedSIgl
dc.description.sponsorshipThis study was supported by grants from the Spanish Government, Ministerio de Ciencia e Innovación (PSI2017- 89389-C2-R and PID2020-114521RB-C21/C22); the Galician Government, Axudas para a Consolidación e Estruturación de Unidades de Investigación Competitivas do Sistema Universitario de Galicia: GRC (GI-1807- USC); Refs: ED431-2017/27 and ED431C-2021/04; all with ERDF/FEDER fundsgl
dc.identifier.citationRivas-Fernández MÁ, Lindín M, Zurrón M, Díaz F, Aldrey-Vázquez JM, Pías-Peleteiro JM, Vázquez-Vázquez L, Pereiro AX, Lojo-Seoane C, Nieto-Vieites A and Galdo-Álvarez S (2022) Brain atrophy and clinical characterization of adults with mild cognitive impairment and different cerebrospinal fluid biomarker profiles according to the AT(N) research framework of Alzheimer’s disease. Front. Hum. Neurosci. 16:799347gl
dc.identifier.doi10.3389/fnhum.2022.799347
dc.identifier.issn1662-5161
dc.identifier.urihttp://hdl.handle.net/10347/29974
dc.language.isoenggl
dc.publisherFrontiers Mediagl
dc.relation.publisherversionhttps://doi.org/10.3389/fnhum.2022.799347gl
dc.rightsCopyright © 2022 Rivas-Fernández, Lindín, Zurrón, Díaz, Aldrey-Vázquez, Pías-Peleteiro, Vázquez-Vázquez, Pereiro, Lojo-Seoane, Nieto-Vieites and Galdo-Álvarez. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). (https://creativecommons.org/licenses/by/4.0/)gl
dc.rights.accessRightsopen accessgl
dc.subjectAlzheimer’s Disease (AD)gl
dc.subjectAT(N)gl
dc.subjectAmyloidgl
dc.subjectTaugl
dc.subjectStructural magnetic resonance imaging (sMRI)gl
dc.subjectClinical diagnosisgl
dc.titleBrain atrophy and clinical characterization of adults with mild cognitive impairment and different cerebrospinal fluid biomarker profiles according to the AT(N) research framework of Alzheimer’s diseasegl
dc.typejournal articlegl
dc.type.hasVersionVoRgl
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscovery8196724e-69d9-4175-8f4f-13499f0cd60f

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