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Neural Correlates of Anosognosia in Alzheimer's Disease and Mild Cognitive Impairment: A Multi-Method Assessment

Patients with Alzheimer's Disease (AD) and Mild Cognitive Impairment (MCI) may present anosognosia for their cognitive deficits. Three different methods have been usually used to measure anosognosia in patients with AD and MCI, but no studies have established if they share similar neuroanatomic...

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Autores principales: Tondelli, Manuela, Barbarulo, Anna M., Vinceti, Giulia, Vincenzi, Chiara, Chiari, Annalisa, Nichelli, Paolo F., Zamboni, Giovanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5966556/
https://www.ncbi.nlm.nih.gov/pubmed/29867398
http://dx.doi.org/10.3389/fnbeh.2018.00100
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author Tondelli, Manuela
Barbarulo, Anna M.
Vinceti, Giulia
Vincenzi, Chiara
Chiari, Annalisa
Nichelli, Paolo F.
Zamboni, Giovanna
author_facet Tondelli, Manuela
Barbarulo, Anna M.
Vinceti, Giulia
Vincenzi, Chiara
Chiari, Annalisa
Nichelli, Paolo F.
Zamboni, Giovanna
author_sort Tondelli, Manuela
collection PubMed
description Patients with Alzheimer's Disease (AD) and Mild Cognitive Impairment (MCI) may present anosognosia for their cognitive deficits. Three different methods have been usually used to measure anosognosia in patients with AD and MCI, but no studies have established if they share similar neuroanatomical correlates. The purpose of this study was to investigate if anosognosia scores obtained with the three most commonly used methods to assess anosognosia relate to focal atrophy in AD and MCI patients, in order to improve understanding of the neural basis of anosognosia in dementia. Anosognosia was evaluated in 27 patients (15 MCI and 12 AD) through clinical rating (Clinical Insight Rating Scale, CIRS), patient-informant discrepancy (Anosognosia Questionnaire Dementia, AQ-D), and performance discrepancy on different cognitive domains (self-appraisal discrepancies, SADs). Voxel-based morphometry correlational analyses were performed on magnetic resonance imaging (MRI) data with each anosognosia score. Increasing anosognosia on any anosognosia measurement (CIRS, AQ-D, SADs) was associated with increasing gray matter atrophy in the medial temporal lobe including the right hippocampus. Our results support a unitary mechanism of anosognosia in AD and MCI, in which medial temporal lobes play a key role, irrespectively of the assessment method used. This is in accordance with models suggesting that anosognosia in AD is primarily caused by a decline in mnemonic processes.
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spelling pubmed-59665562018-06-04 Neural Correlates of Anosognosia in Alzheimer's Disease and Mild Cognitive Impairment: A Multi-Method Assessment Tondelli, Manuela Barbarulo, Anna M. Vinceti, Giulia Vincenzi, Chiara Chiari, Annalisa Nichelli, Paolo F. Zamboni, Giovanna Front Behav Neurosci Neuroscience Patients with Alzheimer's Disease (AD) and Mild Cognitive Impairment (MCI) may present anosognosia for their cognitive deficits. Three different methods have been usually used to measure anosognosia in patients with AD and MCI, but no studies have established if they share similar neuroanatomical correlates. The purpose of this study was to investigate if anosognosia scores obtained with the three most commonly used methods to assess anosognosia relate to focal atrophy in AD and MCI patients, in order to improve understanding of the neural basis of anosognosia in dementia. Anosognosia was evaluated in 27 patients (15 MCI and 12 AD) through clinical rating (Clinical Insight Rating Scale, CIRS), patient-informant discrepancy (Anosognosia Questionnaire Dementia, AQ-D), and performance discrepancy on different cognitive domains (self-appraisal discrepancies, SADs). Voxel-based morphometry correlational analyses were performed on magnetic resonance imaging (MRI) data with each anosognosia score. Increasing anosognosia on any anosognosia measurement (CIRS, AQ-D, SADs) was associated with increasing gray matter atrophy in the medial temporal lobe including the right hippocampus. Our results support a unitary mechanism of anosognosia in AD and MCI, in which medial temporal lobes play a key role, irrespectively of the assessment method used. This is in accordance with models suggesting that anosognosia in AD is primarily caused by a decline in mnemonic processes. Frontiers Media S.A. 2018-05-17 /pmc/articles/PMC5966556/ /pubmed/29867398 http://dx.doi.org/10.3389/fnbeh.2018.00100 Text en Copyright © 2018 Tondelli, Barbarulo, Vinceti, Vincenzi, Chiari, Nichelli and Zamboni. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Tondelli, Manuela
Barbarulo, Anna M.
Vinceti, Giulia
Vincenzi, Chiara
Chiari, Annalisa
Nichelli, Paolo F.
Zamboni, Giovanna
Neural Correlates of Anosognosia in Alzheimer's Disease and Mild Cognitive Impairment: A Multi-Method Assessment
title Neural Correlates of Anosognosia in Alzheimer's Disease and Mild Cognitive Impairment: A Multi-Method Assessment
title_full Neural Correlates of Anosognosia in Alzheimer's Disease and Mild Cognitive Impairment: A Multi-Method Assessment
title_fullStr Neural Correlates of Anosognosia in Alzheimer's Disease and Mild Cognitive Impairment: A Multi-Method Assessment
title_full_unstemmed Neural Correlates of Anosognosia in Alzheimer's Disease and Mild Cognitive Impairment: A Multi-Method Assessment
title_short Neural Correlates of Anosognosia in Alzheimer's Disease and Mild Cognitive Impairment: A Multi-Method Assessment
title_sort neural correlates of anosognosia in alzheimer's disease and mild cognitive impairment: a multi-method assessment
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5966556/
https://www.ncbi.nlm.nih.gov/pubmed/29867398
http://dx.doi.org/10.3389/fnbeh.2018.00100
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