
Impairment of episodic memory in genetic frontotemporal dementia: A GENFI study
Author(s) -
Poos Jackie M.,
Russell Lucy L.,
Peakman Georgia,
Bocchetta Martina,
Greaves Caroline V.,
Jiskoot Lize C.,
Ende Emma L.,
Seelaar Harro,
Papma Janne M.,
den Berg Esther,
Pijnenburg Yolande A.L.,
Borroni Barbara,
SanchezValle Raquel,
Moreno Fermin,
Laforce Robert,
Graff Caroline,
Synofzik Matthias,
Galimberti Daniela,
Rowe James B.,
Masellis Mario,
Tartaglia Carmela,
Finger Elizabeth,
Vandenberghe Rik,
Medonça Alexandre,
Tagliavini Fabrizio,
Butler Chris R.,
Santana Isabel,
Ber Isabelle Le,
Gerhard Alex,
Ducharme Simon,
Levin Johannes,
Danek Adrian,
Otto Markus,
Sorbi Sandro,
Pasquier Florence,
Swieten John C.,
Rohrer Jonathan D.
Publication year - 2021
Publication title -
alzheimer's and dementia: diagnosis, assessment and disease monitoring
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.497
H-Index - 37
ISSN - 2352-8729
DOI - 10.1002/dad2.12185
Subject(s) - frontotemporal dementia , c9orf72 , psychology , episodic memory , neuropsychology , dementia , neuroscience , medicine , cognition , disease
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.