Cargando…

Narrative impairment, white matter damage and CSF biomarkers in the Alzheimer’s disease spectrum

Background: Narrative discourse (ND) refers to one’s ability to verbally reproduce a sequence of temporally and logically-linked events. Impairments in ND may occur in subjects with Amnestic Mild Cognitive Impairment (aMCI) and Alzheimer’s Disease (AD), but correlates across this function, neuroimag...

Descripción completa

Detalles Bibliográficos
Autores principales: Drummond, Claudia, Coutinho, Gabriel, Monteiro, Marina Carneiro, Assuncao, Naima, Teldeschi, Alina, de Souza, Andrea Silveira, Oliveira, Natalia, Bramati, Ivanei, Sudo, Felipe Kenji, Vanderboght, Bart, Brandao, Carlos Otavio, Fonseca, Rochele Paz, de Oliveira-Souza, Ricardo, Moll, Jorge, Mattos, Paulo, Tovar-Moll, Fernanda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6834410/
https://www.ncbi.nlm.nih.gov/pubmed/31682234
http://dx.doi.org/10.18632/aging.102391
Descripción
Sumario:Background: Narrative discourse (ND) refers to one’s ability to verbally reproduce a sequence of temporally and logically-linked events. Impairments in ND may occur in subjects with Amnestic Mild Cognitive Impairment (aMCI) and Alzheimer’s Disease (AD), but correlates across this function, neuroimaging and cerebrospinal fluid (CSF) AD biomarkers remain understudied. Objectives: We sought to measure correlates among ND, Diffusion Tensor Imaging (DTI) indexes and AD CSF biomarkers in patients within the AD spectrum. Results: Groups differed in narrative production (NProd) and comprehension. aMCI and AD presented poorer inference abilities than controls. AD subjects were more impaired than controls and aMCI regarding WB (p<0.01). ROIs DTI assessment distinguished the three groups. Mean Diffusivity (MD) in the uncinate, bilateral parahippocampal cingulate and left inferior occipitofrontal fasciculi negatively correlated with NProd. Changes in specific tracts correlated with T-tau/Aβ1-42 ratio in CSF. Conclusions: AD and aMCI patients presented more ND impairments than controls. Those findings were associated with changes in ventral language-associated and in the inferior parahippocampal pathways. The latest were correlated with biomarkers’ levels in the CSF. Methods: AD (N=14), aMCI (N=31) and Control (N=39) groups were compared for whole brain (WB) and regions of interest (ROI) DTI parameters, ND and AD CSF biomarkers.