TY - JOUR
T1 - Multimodal neurocognitive markers of naturalistic discourse typify diverse neurodegenerative diseases
AU - Birba, Agustina
AU - Fittipaldi, Sol
AU - Cediel Escobar, Judith C.
AU - Gonzalez Campo, Cecilia
AU - Legaz, Agustina
AU - Galiani, Agostina
AU - Rivera, Mariano N.Díaz
AU - Caro, Miquel Martorell
AU - Alifano, Florencia
AU - Piña-Escudero, Stefanie D.
AU - Cardona, Juan Felipe
AU - Neely, Alejandra
AU - Forno, Gonzalo
AU - Carpinella, Mariela
AU - Slachevsky, Andrea
AU - Serrano, Cecilia
AU - Sedeño, Lucas
AU - Ibáñez, Agustín
AU - García, Adolfo M.
N1 - Publisher Copyright:
© 2021 The Author(s). Published by Oxford University Press. All rights reserved.
PY - 2022/8/15
Y1 - 2022/8/15
N2 - Neurodegeneration has multiscalar impacts, including behavioral, neuroanatomical, and neurofunctional disruptions. Can disease-differential alterations be captured across such dimensions using naturalistic stimuli? To address this question, we assessed comprehension of four naturalistic stories, highlighting action, nonaction, social, and nonsocial events, in Parkinson's disease (PD) and behavioral variant frontotemporal dementia (bvFTD) relative to Alzheimer's disease patients and healthy controls. Text-specific correlates were evaluated via voxel-based morphometry, spatial (fMRI), and temporal (hd-EEG) functional connectivity. PD patients presented action-text deficits related to the volume of action-observation regions, connectivity across motor-related and multimodal-semantic hubs, and frontal hd-EEG hypoconnectivity. BvFTD patients exhibited social-text deficits, associated with atrophy and spatial connectivity patterns along social-network hubs, alongside right frontotemporal hd-EEG hypoconnectivity. Alzheimer's disease patients showed impairments in all stories, widespread atrophy and spatial connectivity patterns, and heightened occipitotemporal hd-EEG connectivity. Our framework revealed disease-specific signatures across behavioral, neuroanatomical, and neurofunctional dimensions, highlighting the sensitivity and specificity of a single naturalistic task. This investigation opens a translational agenda combining ecological approaches and multimodal cognitive neuroscience for the study of neurodegeneration.
AB - Neurodegeneration has multiscalar impacts, including behavioral, neuroanatomical, and neurofunctional disruptions. Can disease-differential alterations be captured across such dimensions using naturalistic stimuli? To address this question, we assessed comprehension of four naturalistic stories, highlighting action, nonaction, social, and nonsocial events, in Parkinson's disease (PD) and behavioral variant frontotemporal dementia (bvFTD) relative to Alzheimer's disease patients and healthy controls. Text-specific correlates were evaluated via voxel-based morphometry, spatial (fMRI), and temporal (hd-EEG) functional connectivity. PD patients presented action-text deficits related to the volume of action-observation regions, connectivity across motor-related and multimodal-semantic hubs, and frontal hd-EEG hypoconnectivity. BvFTD patients exhibited social-text deficits, associated with atrophy and spatial connectivity patterns along social-network hubs, alongside right frontotemporal hd-EEG hypoconnectivity. Alzheimer's disease patients showed impairments in all stories, widespread atrophy and spatial connectivity patterns, and heightened occipitotemporal hd-EEG connectivity. Our framework revealed disease-specific signatures across behavioral, neuroanatomical, and neurofunctional dimensions, highlighting the sensitivity and specificity of a single naturalistic task. This investigation opens a translational agenda combining ecological approaches and multimodal cognitive neuroscience for the study of neurodegeneration.
KW - embodied cognition
KW - fMRI/hd-EEG functional connectivity
KW - naturalistic texts
KW - neurodegeneration
KW - voxel-based morphometry
UR - http://www.scopus.com/inward/record.url?scp=85121227733&partnerID=8YFLogxK
U2 - 10.1093/cercor/bhab421
DO - 10.1093/cercor/bhab421
M3 - Article
C2 - 34875690
AN - SCOPUS:85121227733
SN - 1047-3211
VL - 32
SP - 3377
EP - 3391
JO - Cerebral Cortex
JF - Cerebral Cortex
IS - 16
ER -