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Anosognosia and default mode subnetwork dysfunction in Alzheimer's disease

Research on the neural correlates of anosognosia in Alzheimer's disease varied according to methods and objectives: they compared different measures, used diverse neuroimaging modalities, explored connectivity between brain networks, addressed the role of specific brain regions or tried to give...

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Autores principales: Antoine, Nicolas, Bahri, Mohamed A., Bastin, Christine, Collette, Fabienne, Phillips, Christophe, Balteau, Evelyne, Genon, Sarah, Salmon, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864891/
https://www.ncbi.nlm.nih.gov/pubmed/31444942
http://dx.doi.org/10.1002/hbm.24775
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author Antoine, Nicolas
Bahri, Mohamed A.
Bastin, Christine
Collette, Fabienne
Phillips, Christophe
Balteau, Evelyne
Genon, Sarah
Salmon, Eric
author_facet Antoine, Nicolas
Bahri, Mohamed A.
Bastin, Christine
Collette, Fabienne
Phillips, Christophe
Balteau, Evelyne
Genon, Sarah
Salmon, Eric
author_sort Antoine, Nicolas
collection PubMed
description Research on the neural correlates of anosognosia in Alzheimer's disease varied according to methods and objectives: they compared different measures, used diverse neuroimaging modalities, explored connectivity between brain networks, addressed the role of specific brain regions or tried to give support to theoretical models of unawareness. We used resting‐state fMRI connectivity with two different seed regions and two measures of anosognosia in different patient samples to investigate consistent modifications of default mode subnetworks and we aligned the results with the Cognitive Awareness Model. In a first study, patients and their relatives were presented with the Memory Awareness Rating Scale. Anosognosia was measured as a patient‐relative discrepancy score and connectivity was investigated with a parahippocampal seed. In a second study, anosognosia was measured in patients with brain amyloid (taken as a disease biomarker) by comparing self‐reported rating with memory performance, and connectivity was examined with a hippocampal seed. In both studies, anosognosia was consistently related to disconnection within the medial temporal subsystem of the default mode network, subserving episodic memory processes. Importantly, scores were also related to disconnection between the medial temporal and both the core subsystem (participating to self‐reflection) and the dorsomedial subsystem of the default mode network (the middle temporal gyrus that might subserve a personal database in the second study). We suggest that disparity in connectivity within and between subsystems of the default mode network may reflect impaired functioning of pathways in cognitive models of awareness.
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spelling pubmed-68648912020-06-12 Anosognosia and default mode subnetwork dysfunction in Alzheimer's disease Antoine, Nicolas Bahri, Mohamed A. Bastin, Christine Collette, Fabienne Phillips, Christophe Balteau, Evelyne Genon, Sarah Salmon, Eric Hum Brain Mapp Research Articles Research on the neural correlates of anosognosia in Alzheimer's disease varied according to methods and objectives: they compared different measures, used diverse neuroimaging modalities, explored connectivity between brain networks, addressed the role of specific brain regions or tried to give support to theoretical models of unawareness. We used resting‐state fMRI connectivity with two different seed regions and two measures of anosognosia in different patient samples to investigate consistent modifications of default mode subnetworks and we aligned the results with the Cognitive Awareness Model. In a first study, patients and their relatives were presented with the Memory Awareness Rating Scale. Anosognosia was measured as a patient‐relative discrepancy score and connectivity was investigated with a parahippocampal seed. In a second study, anosognosia was measured in patients with brain amyloid (taken as a disease biomarker) by comparing self‐reported rating with memory performance, and connectivity was examined with a hippocampal seed. In both studies, anosognosia was consistently related to disconnection within the medial temporal subsystem of the default mode network, subserving episodic memory processes. Importantly, scores were also related to disconnection between the medial temporal and both the core subsystem (participating to self‐reflection) and the dorsomedial subsystem of the default mode network (the middle temporal gyrus that might subserve a personal database in the second study). We suggest that disparity in connectivity within and between subsystems of the default mode network may reflect impaired functioning of pathways in cognitive models of awareness. John Wiley & Sons, Inc. 2019-08-24 /pmc/articles/PMC6864891/ /pubmed/31444942 http://dx.doi.org/10.1002/hbm.24775 Text en © 2019 The Authors. Human Brain Mapping published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Antoine, Nicolas
Bahri, Mohamed A.
Bastin, Christine
Collette, Fabienne
Phillips, Christophe
Balteau, Evelyne
Genon, Sarah
Salmon, Eric
Anosognosia and default mode subnetwork dysfunction in Alzheimer's disease
title Anosognosia and default mode subnetwork dysfunction in Alzheimer's disease
title_full Anosognosia and default mode subnetwork dysfunction in Alzheimer's disease
title_fullStr Anosognosia and default mode subnetwork dysfunction in Alzheimer's disease
title_full_unstemmed Anosognosia and default mode subnetwork dysfunction in Alzheimer's disease
title_short Anosognosia and default mode subnetwork dysfunction in Alzheimer's disease
title_sort anosognosia and default mode subnetwork dysfunction in alzheimer's disease
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6864891/
https://www.ncbi.nlm.nih.gov/pubmed/31444942
http://dx.doi.org/10.1002/hbm.24775
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