Cognitive profile of patients with facioscapulohumeral muscular dystrophy

Detalhes bibliográficos
Autor(a) principal: Santos,Vanessa Brzoskowski dos
Data de Publicação: 2021
Outros Autores: Saute,Jonas Alex Morales, Jacinto-Scudeiro,Laís Alves, Ayres,Annelise, Rech,Rafaela Soares, Oliveira,Alcyr Alves de, Olchik,Maira Rozenfeld
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Dementia & Neuropsychologia
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1980-57642021000400541
Resumo: ABSTRACT Although it is predominantly a muscular disease, impairments in the central nervous system in patients with facioscapulohumeral muscular dystrophy (FSHD) have been described in the literature. Objective: To describe the cognitive profile of patients with FSHD and to correlate the impairments found with clinical variables and quality of life. Methods: Cross-sectional and case–control study that evaluated FSHD patients using a series of cognitive assessments (Mini-Mental State Examination — MMSE, Montreal Cognitive Assessment — MoCA, verbal fluency with phonological restriction — FAS, categorical verbal fluency — FAS-cat, trail-making test — TMT, and Rey’s Verbal Auditory Learning Test); a neurological severity scale (Gardner–Medwin–Walton — GMWS); and a quality of life measurement tool (Medical Outcomes Study 36-Item Short-Form Health Survey). Results: Individuals with FSHD (13) and healthy controls (26) were paired by gender and age. Significant differences between case and control groups were found in MMSE, TMT A, and A7 (p≤0.05) and MOCA (p≤0.001) performances. A positive correlation was verified in long-term memory impairments and the age in which symptoms appear (r=-0.593, p=0.033). Regarding quality of life assessment, the emotional domain correlated to MEEM (r=0.657, p=0.015), TMT A (r=-0.601, p=0.030), and A7 (r=0.617, p=0.025) performances. Conclusions: Individuals with FSHD presented mild impairments in the performance of tasks that involve attention, planning, and long-term memory functions. Those impairments were associated neither with the disease duration nor with its neurological severity.
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spelling Cognitive profile of patients with facioscapulohumeral muscular dystrophymuscular dystrophiesneuromuscular diseasescognitionquality of lifeABSTRACT Although it is predominantly a muscular disease, impairments in the central nervous system in patients with facioscapulohumeral muscular dystrophy (FSHD) have been described in the literature. Objective: To describe the cognitive profile of patients with FSHD and to correlate the impairments found with clinical variables and quality of life. Methods: Cross-sectional and case–control study that evaluated FSHD patients using a series of cognitive assessments (Mini-Mental State Examination — MMSE, Montreal Cognitive Assessment — MoCA, verbal fluency with phonological restriction — FAS, categorical verbal fluency — FAS-cat, trail-making test — TMT, and Rey’s Verbal Auditory Learning Test); a neurological severity scale (Gardner–Medwin–Walton — GMWS); and a quality of life measurement tool (Medical Outcomes Study 36-Item Short-Form Health Survey). Results: Individuals with FSHD (13) and healthy controls (26) were paired by gender and age. Significant differences between case and control groups were found in MMSE, TMT A, and A7 (p≤0.05) and MOCA (p≤0.001) performances. A positive correlation was verified in long-term memory impairments and the age in which symptoms appear (r=-0.593, p=0.033). Regarding quality of life assessment, the emotional domain correlated to MEEM (r=0.657, p=0.015), TMT A (r=-0.601, p=0.030), and A7 (r=0.617, p=0.025) performances. Conclusions: Individuals with FSHD presented mild impairments in the performance of tasks that involve attention, planning, and long-term memory functions. Those impairments were associated neither with the disease duration nor with its neurological severity.Academia Brasileira de Neurologia, Departamento de Neurologia Cognitiva e Envelhecimento2021-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1980-57642021000400541Dementia & Neuropsychologia v.15 n.4 2021reponame:Dementia & Neuropsychologiainstname:Associação de Neurologia Cognitiva e do Comportamento (ANCC)instacron:ANCC10.1590/1980-57642021dn15-040015info:eu-repo/semantics/openAccessSantos,Vanessa Brzoskowski dosSaute,Jonas Alex MoralesJacinto-Scudeiro,Laís AlvesAyres,AnneliseRech,Rafaela SoaresOliveira,Alcyr Alves deOlchik,Maira Rozenfeldeng2021-12-01T00:00:00Zoai:scielo:S1980-57642021000400541Revistahttp://www.demneuropsy.com.br/ONGhttps://old.scielo.br/oai/scielo-oai.php||demneuropsy@uol.com.br1980-57641980-5764opendoar:2021-12-01T00:00Dementia & Neuropsychologia - Associação de Neurologia Cognitiva e do Comportamento (ANCC)false
dc.title.none.fl_str_mv Cognitive profile of patients with facioscapulohumeral muscular dystrophy
title Cognitive profile of patients with facioscapulohumeral muscular dystrophy
spellingShingle Cognitive profile of patients with facioscapulohumeral muscular dystrophy
Santos,Vanessa Brzoskowski dos
muscular dystrophies
neuromuscular diseases
cognition
quality of life
title_short Cognitive profile of patients with facioscapulohumeral muscular dystrophy
title_full Cognitive profile of patients with facioscapulohumeral muscular dystrophy
title_fullStr Cognitive profile of patients with facioscapulohumeral muscular dystrophy
title_full_unstemmed Cognitive profile of patients with facioscapulohumeral muscular dystrophy
title_sort Cognitive profile of patients with facioscapulohumeral muscular dystrophy
author Santos,Vanessa Brzoskowski dos
author_facet Santos,Vanessa Brzoskowski dos
Saute,Jonas Alex Morales
Jacinto-Scudeiro,Laís Alves
Ayres,Annelise
Rech,Rafaela Soares
Oliveira,Alcyr Alves de
Olchik,Maira Rozenfeld
author_role author
author2 Saute,Jonas Alex Morales
Jacinto-Scudeiro,Laís Alves
Ayres,Annelise
Rech,Rafaela Soares
Oliveira,Alcyr Alves de
Olchik,Maira Rozenfeld
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Santos,Vanessa Brzoskowski dos
Saute,Jonas Alex Morales
Jacinto-Scudeiro,Laís Alves
Ayres,Annelise
Rech,Rafaela Soares
Oliveira,Alcyr Alves de
Olchik,Maira Rozenfeld
dc.subject.por.fl_str_mv muscular dystrophies
neuromuscular diseases
cognition
quality of life
topic muscular dystrophies
neuromuscular diseases
cognition
quality of life
description ABSTRACT Although it is predominantly a muscular disease, impairments in the central nervous system in patients with facioscapulohumeral muscular dystrophy (FSHD) have been described in the literature. Objective: To describe the cognitive profile of patients with FSHD and to correlate the impairments found with clinical variables and quality of life. Methods: Cross-sectional and case–control study that evaluated FSHD patients using a series of cognitive assessments (Mini-Mental State Examination — MMSE, Montreal Cognitive Assessment — MoCA, verbal fluency with phonological restriction — FAS, categorical verbal fluency — FAS-cat, trail-making test — TMT, and Rey’s Verbal Auditory Learning Test); a neurological severity scale (Gardner–Medwin–Walton — GMWS); and a quality of life measurement tool (Medical Outcomes Study 36-Item Short-Form Health Survey). Results: Individuals with FSHD (13) and healthy controls (26) were paired by gender and age. Significant differences between case and control groups were found in MMSE, TMT A, and A7 (p≤0.05) and MOCA (p≤0.001) performances. A positive correlation was verified in long-term memory impairments and the age in which symptoms appear (r=-0.593, p=0.033). Regarding quality of life assessment, the emotional domain correlated to MEEM (r=0.657, p=0.015), TMT A (r=-0.601, p=0.030), and A7 (r=0.617, p=0.025) performances. Conclusions: Individuals with FSHD presented mild impairments in the performance of tasks that involve attention, planning, and long-term memory functions. Those impairments were associated neither with the disease duration nor with its neurological severity.
publishDate 2021
dc.date.none.fl_str_mv 2021-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1980-57642021000400541
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1980-57642021000400541
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1980-57642021dn15-040015
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Academia Brasileira de Neurologia, Departamento de Neurologia Cognitiva e Envelhecimento
publisher.none.fl_str_mv Academia Brasileira de Neurologia, Departamento de Neurologia Cognitiva e Envelhecimento
dc.source.none.fl_str_mv Dementia & Neuropsychologia v.15 n.4 2021
reponame:Dementia & Neuropsychologia
instname:Associação de Neurologia Cognitiva e do Comportamento (ANCC)
instacron:ANCC
instname_str Associação de Neurologia Cognitiva e do Comportamento (ANCC)
instacron_str ANCC
institution ANCC
reponame_str Dementia & Neuropsychologia
collection Dementia & Neuropsychologia
repository.name.fl_str_mv Dementia & Neuropsychologia - Associação de Neurologia Cognitiva e do Comportamento (ANCC)
repository.mail.fl_str_mv ||demneuropsy@uol.com.br
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