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Neuropsychological features of progranulin-associated frontotemporal dementia: a nested case-control study

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Resumo:The distinction between sporadic and genetic behavioural-variant frontotemporal dementia (bvFTD) regarding some neuropsychological (NP) features remains challenging. Specifically, progranulin (GRN)-associated bvFTD frequently presents with early episodic memory impairment and some degree of parietal dysfunction which are supporters of Alzheimer's disease (AD) diagnosis. In this context, we aimed to characterize the NP profile of GRN-bvFTD as compared to sporadic-bvFTD and AD in patients with mild dementia (Mini-Mental State Examination score ≥ 17 and Clinical Dementia Rating Scale score ≤ 1. We identified 21 patients at Centro Hospitalar e Universitário de Coimbra, Portugal with GRN mutations belonging to fifteen different families. As our focus was bvFTD variants, FTD-related aphasic forms (3 patients) were excluded. The remaining 18 GRN-bvFTD were further matched with 18 sporadic-bvFTD and 18 AD patients according to disease staging, age and education. All patients completed the Mini-Mental State Examination, Montreal Cognitive Assessment (MoCA) and a comprehensive NP assessment battery. Results were converted into z-scores. Differences between groups in individual NP measures and NP domains were assessed through non-parametric tests (Kruskal-Wallis test analysis) and eta squared (ŋ2) was calculated as a measure of effect size. Group comparisons show that GRN patients have worse performances on verbal retrieval processes (P = 0.039, ŋ2 = 0.110) and visuoconstructive abilities (P = 0.039, ŋ2 = 0.190) than sporadic bvFTD forms. When compared to AD, GRN patients present a higher impairment in frontal (P = 0.001, ŋ2 = 0.211) and parietal (P = 0.041, ŋ2 = 0.129) measures and a better performance in memory tasks (P = 0.020, ŋ2 = 0.120). Sporadic-bvFTD forms are worse than AD in frontal measures (P = 0.032, ŋ2 = 0.200), being better in both memory (P = 0.010, ŋ2 = 0.131) and visuospatial skills (P = 0.023, ŋ2 = 0.231). Considering these results, we conclude that GRN-bvFTD patients present a NP profile that associates the typical patterns of FTD and AD deficits. This is particularly expressive in visuoconstructive abilities, which was the more discriminative feature between groups, followed by episodic verbal memory. This study was approved by the Institutional Ethics Committee of Centro Hospitalar e Universitário de Coimbra, Portugal (CE-029/2019) on June 24, 2019.
Autores principais:Lima, Marisa
Outros Autores:Lima, Marisa; Lima, Marisa; Lima, M.; Center for Research in Neuropsychology and Cognitive Behavioral Intervention (CINEICC); Center for Research in Neuropsychology and Cognitive Behavioral Intervention (CINEICC); Rijo, Daniel; Rijo, Daniel; Rijo, Daniel Maria Bugalho; CINEICC – Center for Research in Neuropsychology and Cognitive and Behavioural Intervention; drijo@fpce.uc.pt; 0000-0002-5368-0770; 41361723000; V-7419-2017; staff; Faculty of Psychology and Educational Sciences; Faculty of Psychology and Educational Sciences; organization; Ferreira, Cláudia; Ferreira, Cláudia; Ferreira, Cláudia Rute Carlos; Center for Research in Neuropsychology and Cognitive Behavioral Intervention (CINEICC); claudiaferreira@fpce.uc.pt; 0000-0002-7020-9606; 55971706100; staff; Cláudia Ferreira. Concluiu o Doutoramento em Psicologia em 2012 pela Universidade de Coimbra Faculdade de Psicologia e de Ciências da Educação. É Professor Auxiliar na Faculdade de Psicologia e de Ciências da Educação da Universidade de Coimbra. Publicou 90 artigos em revistas especializadas. Possui 1 capítulo(s) de livros. Coorientou 4 tese(s) de doutoramento. Orientou 30 dissertação(ões) de mestrado e coorientou 20. Participa e/ou participou como Investigador em 5 projeto(s) e Investigador responsável em 1 projeto. Nas suas atividades profissionais interagiu com 116 colaborador(es) em coautorias de trabalhos científicos.; Fonseca, A.; Fonseca, A.; Fonseca, A.; PT; 0000-0003-4200-9284; staff; Tábuas-Pereira, Miguel; Tábuas-Pereira, Miguel; Duro, Diana; Duro, Diana; Duro, Diana; Center for Research in Neuropsychology and Cognitive Behavioral Intervention (CINEICC); Center for Research in Neuropsychology and Cognitive Behavioral Intervention (CINEICC); Rijo, Daniel; Rijo, Daniel; Rijo, Daniel Maria Bugalho; CINEICC – Center for Research in Neuropsychology and Cognitive and Behavioural Intervention; drijo@fpce.uc.pt; 0000-0002-5368-0770; 41361723000; V-7419-2017; staff; Faculty of Psychology and Educational Sciences; Faculty of Psychology and Educational Sciences; organization; Ferreira, Cláudia; Ferreira, Cláudia; Ferreira, Cláudia Rute Carlos; Center for Research in Neuropsychology and Cognitive Behavioral Intervention (CINEICC); claudiaferreira@fpce.uc.pt; 0000-0002-7020-9606; 55971706100; staff; Cláudia Ferreira. Concluiu o Doutoramento em Psicologia em 2012 pela Universidade de Coimbra Faculdade de Psicologia e de Ciências da Educação. É Professor Auxiliar na Faculdade de Psicologia e de Ciências da Educação da Universidade de Coimbra. Publicou 90 artigos em revistas especializadas. Possui 1 capítulo(s) de livros. Coorientou 4 tese(s) de doutoramento. Orientou 30 dissertação(ões) de mestrado e coorientou 20. Participa e/ou participou como Investigador em 5 projeto(s) e Investigador responsável em 1 projeto. Nas suas atividades profissionais interagiu com 116 colaborador(es) em coautorias de trabalhos científicos.; Fonseca, A.; Fonseca, A.; Fonseca, A.; PT; 0000-0002-9818-9862; 24922627100; C-1588-2015; staff; Durães, João; Durães, João; Vieira, Daniela; Vieira, Daniela; Baldeiras, Inês; Baldeiras, Inês; Baldeiras, Inês E.; Baldeiras, I.; Baldeiras, Inês E.; CNC - Center for Neuroscience and Cell Biology; CNC - Center for Neuroscience and Cell Biology; Almeida, Luís P. de; Almeida, Luís Pereira de; Almeida, Luís P. de; Almeida, Luís; Almeida, Luís Pereira de; Almeida, Luís; Almeida, L. P.; Almeida, Luís Fernando Morgado Pereira de; CIBB - Center for Innovative Biomedicine and Biotechnology; GeneT- Centro de Excelência em Terapia Génica em Portugal; CNC - Center for Neuroscience and Cell Biology; luispa@ci.uc.pt; luispa@ff.uc.pt; luispa@cnc.uc.pt; lpereiradealmeida@gmail.com; 0000-0001-5831-3307; 5911-1D34-FB6B; A-4605-2009; staff; research; Coimbra; PT; 0000-0002-8106-7308; 15065184000; staff; Almeida, Maria do Rosário; Almeida, Maria R.; Almeida, Maria do Rosário; 0000-0002-1889-5469; 511D-162F-AE5C; staff; Santana, Isabel; Santana, Isabel; Santana, Isabel; Santana, Isabel; Santana, I.; CNC - Center for Neuroscience and Cell Biology; CNC - Center for Neuroscience and Cell Biology; Almeida, Luís P. de; Almeida, Luís Pereira de; Almeida, Luís P. de; Almeida, Luís; Almeida, Luís Pereira de; Almeida, Luís; Almeida, L. P.; Almeida, Luís Fernando Morgado Pereira de; GeneT- Centro de Excelência em Terapia Génica em Portugal; CNC - Center for Neuroscience and Cell Biology; CIBB - Center for Innovative Biomedicine and Biotechnology; luispa@ci.uc.pt; luispa@ff.uc.pt; luispa@cnc.uc.pt; lpereiradealmeida@gmail.com; 0000-0001-5831-3307; 5911-1D34-FB6B; A-4605-2009; staff; research; Coimbra; PT; 0000-0002-8114-9434; C114-9E4C-3B3D; 6603922366; staff; Maria Isabel Jacinto Santana graduated in Medicine at the University of Coimbra in 1984, completed is PhD in Neurology (Alzheimer's Disease) in 1999 and is Full Professor of Neurology at the Faculty of Medicine of the University of Coimbra and co-coordinator of the Neurosciences and Mental Health Group since 2019. She is the director of the Neurology Department at the Centro Hospitalar e Universitário de Coimbra, being head of the Memory/Dementia Clinic and the Neuropsychological Unit and coordinator of the Coimbra Center at the European Alzheimers disease Consortium (EADC). Her main areas of expertise are neurodegenerative diseases in both clinical practise and translational investigation, including 20 years of experience in clinical trials and is a member of the National Ethics Committee for Clinical Investigation (CEIC) since 2017. As an integrated Member of the Center for Neuroscience and Cell Biology (CNC-UC) and head of the clinical/translational research group "Biomarkers in Neuropsychiatric Disorders: from Molecules to Diagnosis and Intervention" of the Center for Innovative Biomedicine and Biotechnology. She participates and/or has participated as Principal investigator in 13 project(s) and as Researcher in 26 project(s) with competitive financial support, received 26 awards and/or honors, is author/co-author of over 250 papers (6492 citations/h factor: 41), 31 books/section(s) of books and of more than 500 oral presentations in national and/or international scientific meetings. She has supervised/co-supervised 10 PhD thesis and 51 MSc dissertations.
Assunto:Alzheimer’s disease behavioral variant frontotemporal dementia cognitive profile frontotemporal dementia genetics memory neuropsychology progranulin visuoconstructive ability
Ano:2021
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso aberto
Instituição associada:Universidade de Coimbra
Idioma:inglês
Origem:Estudo Geral - Universidade de Coimbra
Descrição
Resumo:The distinction between sporadic and genetic behavioural-variant frontotemporal dementia (bvFTD) regarding some neuropsychological (NP) features remains challenging. Specifically, progranulin (GRN)-associated bvFTD frequently presents with early episodic memory impairment and some degree of parietal dysfunction which are supporters of Alzheimer's disease (AD) diagnosis. In this context, we aimed to characterize the NP profile of GRN-bvFTD as compared to sporadic-bvFTD and AD in patients with mild dementia (Mini-Mental State Examination score ≥ 17 and Clinical Dementia Rating Scale score ≤ 1. We identified 21 patients at Centro Hospitalar e Universitário de Coimbra, Portugal with GRN mutations belonging to fifteen different families. As our focus was bvFTD variants, FTD-related aphasic forms (3 patients) were excluded. The remaining 18 GRN-bvFTD were further matched with 18 sporadic-bvFTD and 18 AD patients according to disease staging, age and education. All patients completed the Mini-Mental State Examination, Montreal Cognitive Assessment (MoCA) and a comprehensive NP assessment battery. Results were converted into z-scores. Differences between groups in individual NP measures and NP domains were assessed through non-parametric tests (Kruskal-Wallis test analysis) and eta squared (ŋ2) was calculated as a measure of effect size. Group comparisons show that GRN patients have worse performances on verbal retrieval processes (P = 0.039, ŋ2 = 0.110) and visuoconstructive abilities (P = 0.039, ŋ2 = 0.190) than sporadic bvFTD forms. When compared to AD, GRN patients present a higher impairment in frontal (P = 0.001, ŋ2 = 0.211) and parietal (P = 0.041, ŋ2 = 0.129) measures and a better performance in memory tasks (P = 0.020, ŋ2 = 0.120). Sporadic-bvFTD forms are worse than AD in frontal measures (P = 0.032, ŋ2 = 0.200), being better in both memory (P = 0.010, ŋ2 = 0.131) and visuospatial skills (P = 0.023, ŋ2 = 0.231). Considering these results, we conclude that GRN-bvFTD patients present a NP profile that associates the typical patterns of FTD and AD deficits. This is particularly expressive in visuoconstructive abilities, which was the more discriminative feature between groups, followed by episodic verbal memory. This study was approved by the Institutional Ethics Committee of Centro Hospitalar e Universitário de Coimbra, Portugal (CE-029/2019) on June 24, 2019.