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Cognitive Reserve in Granulin-Related Frontotemporal Dementia: from Preclinical to Clinical Stages

OBJECTIVE: Consistent with the cognitive reserve hypothesis, higher education and occupation attainments may help persons with neurodegenerative dementias to better withstand neuropathology before developing cognitive impairment. We tested here the cognitive reserve hypothesis in patients with front...

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Autores principales: Premi, Enrico, Gazzina, Stefano, Bozzali, Marco, Archetti, Silvana, Alberici, Antonella, Cercignani, Mara, Bianchetti, Angelo, Gasparotti, Roberto, Turla, Marinella, Caltagirone, Carlo, Padovani, Alessandro, Borroni, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767639/
https://www.ncbi.nlm.nih.gov/pubmed/24040338
http://dx.doi.org/10.1371/journal.pone.0074762
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author Premi, Enrico
Gazzina, Stefano
Bozzali, Marco
Archetti, Silvana
Alberici, Antonella
Cercignani, Mara
Bianchetti, Angelo
Gasparotti, Roberto
Turla, Marinella
Caltagirone, Carlo
Padovani, Alessandro
Borroni, Barbara
author_facet Premi, Enrico
Gazzina, Stefano
Bozzali, Marco
Archetti, Silvana
Alberici, Antonella
Cercignani, Mara
Bianchetti, Angelo
Gasparotti, Roberto
Turla, Marinella
Caltagirone, Carlo
Padovani, Alessandro
Borroni, Barbara
author_sort Premi, Enrico
collection PubMed
description OBJECTIVE: Consistent with the cognitive reserve hypothesis, higher education and occupation attainments may help persons with neurodegenerative dementias to better withstand neuropathology before developing cognitive impairment. We tested here the cognitive reserve hypothesis in patients with frontotemporal dementia (FTD), with or without pathogenetic granulin mutations (GRN+ and GRN-), and in presymptomatic GRN mutation carriers (aGRN+). METHODS: Education and occupation attainments were assessed and combined to define Reserve Index (RI) in 32 FTD patients, i.e. 12 GRN+ and 20 GRN-, and in 17 aGRN+. Changes in functional connectivity were estimated by resting state fMRI, focusing on the salience network (SN), executive network (EN) and bilateral frontoparietal networks (FPNs). Cognitive status was measured by FTD-modified Clinical Dementia Rating Scale. RESULTS: In FTD patients higher level of premorbid cognitive reserve was associated with reduced connectivity within the SN and the EN. EN was more involved in FTD patients without GRN mutations, while SN was more affected in GRN pathology. In aGRN+, cognitive reserve was associated with reduced SN. CONCLUSIONS: This study suggests that cognitive reserve modulates functional connectivity in patients with FTD, even in monogenic disease. In GRN inherited FTD, cognitive reserve mechanisms operate even in presymptomatic to clinical stages.
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spelling pubmed-37676392013-09-13 Cognitive Reserve in Granulin-Related Frontotemporal Dementia: from Preclinical to Clinical Stages Premi, Enrico Gazzina, Stefano Bozzali, Marco Archetti, Silvana Alberici, Antonella Cercignani, Mara Bianchetti, Angelo Gasparotti, Roberto Turla, Marinella Caltagirone, Carlo Padovani, Alessandro Borroni, Barbara PLoS One Research Article OBJECTIVE: Consistent with the cognitive reserve hypothesis, higher education and occupation attainments may help persons with neurodegenerative dementias to better withstand neuropathology before developing cognitive impairment. We tested here the cognitive reserve hypothesis in patients with frontotemporal dementia (FTD), with or without pathogenetic granulin mutations (GRN+ and GRN-), and in presymptomatic GRN mutation carriers (aGRN+). METHODS: Education and occupation attainments were assessed and combined to define Reserve Index (RI) in 32 FTD patients, i.e. 12 GRN+ and 20 GRN-, and in 17 aGRN+. Changes in functional connectivity were estimated by resting state fMRI, focusing on the salience network (SN), executive network (EN) and bilateral frontoparietal networks (FPNs). Cognitive status was measured by FTD-modified Clinical Dementia Rating Scale. RESULTS: In FTD patients higher level of premorbid cognitive reserve was associated with reduced connectivity within the SN and the EN. EN was more involved in FTD patients without GRN mutations, while SN was more affected in GRN pathology. In aGRN+, cognitive reserve was associated with reduced SN. CONCLUSIONS: This study suggests that cognitive reserve modulates functional connectivity in patients with FTD, even in monogenic disease. In GRN inherited FTD, cognitive reserve mechanisms operate even in presymptomatic to clinical stages. Public Library of Science 2013-09-09 /pmc/articles/PMC3767639/ /pubmed/24040338 http://dx.doi.org/10.1371/journal.pone.0074762 Text en © 2013 Premi et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Premi, Enrico
Gazzina, Stefano
Bozzali, Marco
Archetti, Silvana
Alberici, Antonella
Cercignani, Mara
Bianchetti, Angelo
Gasparotti, Roberto
Turla, Marinella
Caltagirone, Carlo
Padovani, Alessandro
Borroni, Barbara
Cognitive Reserve in Granulin-Related Frontotemporal Dementia: from Preclinical to Clinical Stages
title Cognitive Reserve in Granulin-Related Frontotemporal Dementia: from Preclinical to Clinical Stages
title_full Cognitive Reserve in Granulin-Related Frontotemporal Dementia: from Preclinical to Clinical Stages
title_fullStr Cognitive Reserve in Granulin-Related Frontotemporal Dementia: from Preclinical to Clinical Stages
title_full_unstemmed Cognitive Reserve in Granulin-Related Frontotemporal Dementia: from Preclinical to Clinical Stages
title_short Cognitive Reserve in Granulin-Related Frontotemporal Dementia: from Preclinical to Clinical Stages
title_sort cognitive reserve in granulin-related frontotemporal dementia: from preclinical to clinical stages
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767639/
https://www.ncbi.nlm.nih.gov/pubmed/24040338
http://dx.doi.org/10.1371/journal.pone.0074762
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