Titre :

Impairment of episodic memory in genetic frontotemporal dementia: A GENFI study.

Auteur(s) :

Poos, Jackie M. [Auteur]
Russell, Lucy L. [Auteur]
Peakman, Georgia [Auteur]
Bocchetta, Martina [Auteur]
Greaves, Caroline V. [Auteur]
Jiskoot, Lize C. [Auteur]
Van Der Ende, Emma L. [Auteur]
Seelaar, Harro [Auteur]
Papma, Janne M. [Auteur]
Pijnenburg, Yolande A. L. [Auteur]
Borroni, Barbara [Auteur]
Sanchez-Valle, Raquel [Auteur]
Moreno, Fermin [Auteur]
Laforce, Robert [Auteur]
Graff, Caroline [Auteur]
Synofzik, Matthias [Auteur]
Galimberti, Daniela [Auteur]
Rowe, James B. [Auteur]
Masellis, Mario [Auteur]
Tartaglia, Carmela [Auteur]
Finger, Elizabeth [Auteur]
Vandenberghe, Rik [Auteur]
De Medonça, Alexandre [Auteur]
Tagliavini, Fabrizio [Auteur]
Butler, Chris R. [Auteur]
Santana, Isabel [Auteur]
Ber, Isabelle Le [Auteur]
Institut du Cerveau = Paris Brain Institute [ICM]
Sorbonne Université [SU]
Gerhard, Alex [Auteur]
Ducharme, Simon [Auteur]
Levin, Johannes [Auteur]
Danek, Adrian [Auteur]
Otto, Markus [Auteur]
Sorbi, Sandro [Auteur]
Pasquier, Florence [Auteur]
Lille Neurosciences & Cognition (LilNCog) - U 1172
Van Swieten, John C. [Auteur]
Rohrer, Jonathan D. [Auteur]

Titre de la revue :

Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring

Numéro :

13

Pagination :

e12185

Date de publication :

2021-05-13

ISSN :

2352-8729

Mot(s)-clé(s) :

cognition
episodic memory
executive function
frontal lobe
frontotemporal dementia
genetic disorders
neuropsychology
temporal lobe
voxel-based morphometry

Discipline(s) HAL :

Sciences du Vivant [q-bio]

Résumé en anglais : [en]

Introduction We aimed to assess episodic memory in genetic frontotemporal dementia (FTD) with the Free and Cued Selective Reminding Test (FCSRT). Methods The FCSRT was administered in 417 presymptomatic and symptomatic ...
Lire la suite >Introduction We aimed to assess episodic memory in genetic frontotemporal dementia (FTD) with the Free and Cued Selective Reminding Test (FCSRT). Methods The FCSRT was administered in 417 presymptomatic and symptomatic mutation carriers (181 chromosome 9 open reading frame 72 [C9orf72], 163 progranulin [GRN], and 73 microtubule-associated protein tau [MAPT]) and 290 controls. Group differences and correlations with other neuropsychological tests were examined. We performed voxel-based morphometry to investigate the underlying neural substrates of the FCSRT. Results All symptomatic mutation carrier groups and presymptomatic MAPT mutation carriers performed significantly worse on all FCSRT scores compared to controls. In the presymptomatic C9orf72 group, deficits were found on all scores except for the delayed total recall task, while no deficits were found in presymptomatic GRN mutation carriers. Performance on the FCSRT correlated with executive function, particularly in C9orf72 mutation carriers, but also with memory and naming tasks in the MAPT group. FCSRT performance also correlated with gray matter volumes of frontal, temporal, and subcortical regions in C9orf72 and GRN, but mainly temporal areas in MAPT mutation carriers. Discussion The FCSRT detects presymptomatic deficits in C9orf72- and MAPT-associated FTD and provides important insight into the underlying cause of memory impairment in different forms of FTD.Lire moins >

Langue :

Anglais

Audience :

Internationale

Vulgarisation :

Non

Établissement(s) :

Université de Lille
Inserm
CHU Lille

Collections :

• Lille Neurosciences & Cognition (LilNCog) - U 1172

Date de dépôt :

2024-01-16T02:08:11Z
2024-11-25T13:26:59Z