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Comparative Study of Subcortical Atrophy in Patients with Frontotemporal Dementia and Dementia with Extrapyramidal Signs

Objectives : To investigate the severity of subcortical atrophy in frontotemporal dementia (FTD) without extrapyramidal symptoms (EPS) and dementia with EPS. In addition, we aim to verify if there is correlation between demographic and clinical characteristics and subcortical atrophy in the groups....

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Autores principales: Caixeta, Leonardo, Vieira, Renata Teles, Paes, Flávia, Carta, Mauro Giovanni, Nardi, Antonio Egidio, Arias-Carrión, Oscar, Rocha, Nuno B. F, Budde, Henning, Machado, Sergio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391205/
https://www.ncbi.nlm.nih.gov/pubmed/25870648
http://dx.doi.org/10.2174/1745017901511010125
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author Caixeta, Leonardo
Vieira, Renata Teles
Paes, Flávia
Carta, Mauro Giovanni
Nardi, Antonio Egidio
Arias-Carrión, Oscar
Rocha, Nuno B. F
Budde, Henning
Machado, Sergio
author_facet Caixeta, Leonardo
Vieira, Renata Teles
Paes, Flávia
Carta, Mauro Giovanni
Nardi, Antonio Egidio
Arias-Carrión, Oscar
Rocha, Nuno B. F
Budde, Henning
Machado, Sergio
author_sort Caixeta, Leonardo
collection PubMed
description Objectives : To investigate the severity of subcortical atrophy in frontotemporal dementia (FTD) without extrapyramidal symptoms (EPS) and dementia with EPS. In addition, we aim to verify if there is correlation between demographic and clinical characteristics and subcortical atrophy in the groups. Methodology : The sample was composed of 21 patients with dementia and EPS as well as 19 patients with FTD without EPS. A linear assessment was conducted in order to identify the degree of subcortical atrophy (i.e., bifrontal index - BFI) using MRI. Moreover, the Mini-Mental State Examination (MMSE), Pfeffer Functional Activities Questionnaire (FAQ) and the Clinical Dementia Rating (CDR) were used to investigate clinical aspects. Results : It was verified that patients with dementia and EPS was older than the patients with FTD (p=0.01). The severity of cognitive deficits was associated with BFI, as well as the dementia severity in the EPS group. Conclusion : FTD group presented mean BFI scores above the cutoff for normal elderly population, indicating the presence of subcortical atrophy in this group. Mean BFI was higher (although not statistically significant) in FTD group than in dementia with EPS, which can suggest at least that subcortical pathology in FTD may be as important as in the dementia with EPS group. Subcortical atrophy is a good biological marker for cognitive deterioration in FTD and in dementia with EPS.
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spelling pubmed-43912052015-04-13 Comparative Study of Subcortical Atrophy in Patients with Frontotemporal Dementia and Dementia with Extrapyramidal Signs Caixeta, Leonardo Vieira, Renata Teles Paes, Flávia Carta, Mauro Giovanni Nardi, Antonio Egidio Arias-Carrión, Oscar Rocha, Nuno B. F Budde, Henning Machado, Sergio Clin Pract Epidemiol Ment Health Article Objectives : To investigate the severity of subcortical atrophy in frontotemporal dementia (FTD) without extrapyramidal symptoms (EPS) and dementia with EPS. In addition, we aim to verify if there is correlation between demographic and clinical characteristics and subcortical atrophy in the groups. Methodology : The sample was composed of 21 patients with dementia and EPS as well as 19 patients with FTD without EPS. A linear assessment was conducted in order to identify the degree of subcortical atrophy (i.e., bifrontal index - BFI) using MRI. Moreover, the Mini-Mental State Examination (MMSE), Pfeffer Functional Activities Questionnaire (FAQ) and the Clinical Dementia Rating (CDR) were used to investigate clinical aspects. Results : It was verified that patients with dementia and EPS was older than the patients with FTD (p=0.01). The severity of cognitive deficits was associated with BFI, as well as the dementia severity in the EPS group. Conclusion : FTD group presented mean BFI scores above the cutoff for normal elderly population, indicating the presence of subcortical atrophy in this group. Mean BFI was higher (although not statistically significant) in FTD group than in dementia with EPS, which can suggest at least that subcortical pathology in FTD may be as important as in the dementia with EPS group. Subcortical atrophy is a good biological marker for cognitive deterioration in FTD and in dementia with EPS. Bentham Open 2015-03-31 /pmc/articles/PMC4391205/ /pubmed/25870648 http://dx.doi.org/10.2174/1745017901511010125 Text en © Caixeta et al.; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Caixeta, Leonardo
Vieira, Renata Teles
Paes, Flávia
Carta, Mauro Giovanni
Nardi, Antonio Egidio
Arias-Carrión, Oscar
Rocha, Nuno B. F
Budde, Henning
Machado, Sergio
Comparative Study of Subcortical Atrophy in Patients with Frontotemporal Dementia and Dementia with Extrapyramidal Signs
title Comparative Study of Subcortical Atrophy in Patients with Frontotemporal Dementia and Dementia with Extrapyramidal Signs
title_full Comparative Study of Subcortical Atrophy in Patients with Frontotemporal Dementia and Dementia with Extrapyramidal Signs
title_fullStr Comparative Study of Subcortical Atrophy in Patients with Frontotemporal Dementia and Dementia with Extrapyramidal Signs
title_full_unstemmed Comparative Study of Subcortical Atrophy in Patients with Frontotemporal Dementia and Dementia with Extrapyramidal Signs
title_short Comparative Study of Subcortical Atrophy in Patients with Frontotemporal Dementia and Dementia with Extrapyramidal Signs
title_sort comparative study of subcortical atrophy in patients with frontotemporal dementia and dementia with extrapyramidal signs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391205/
https://www.ncbi.nlm.nih.gov/pubmed/25870648
http://dx.doi.org/10.2174/1745017901511010125
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