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author Poos, Jackie M.
Russell, Lucy L.
Peakman, Georgia
Bocchetta, Martina
Greaves, Caroline V.
Jiskoot, Lize C.
van der Ende, Emma L.
Seelaar, Harro
Papma, Janne M.
van den Berg, Esther
Pijnenburg, Yolande A.L.
Borroni, Barbara
Sanchez‐Valle, Raquel
Moreno, Fermin
Laforce, Robert
Graff, Caroline
Synofzik, Matthias
Galimberti, Daniela
Rowe, James B.
Masellis, Mario
Tartaglia, Carmela
Finger, Elizabeth
Vandenberghe, Rik
de 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
van Swieten, John C.
Rohrer, Jonathan D.
author_facet Poos, Jackie M.
Russell, Lucy L.
Peakman, Georgia
Bocchetta, Martina
Greaves, Caroline V.
Jiskoot, Lize C.
van der Ende, Emma L.
Seelaar, Harro
Papma, Janne M.
van den Berg, Esther
Pijnenburg, Yolande A.L.
Borroni, Barbara
Sanchez‐Valle, Raquel
Moreno, Fermin
Laforce, Robert
Graff, Caroline
Synofzik, Matthias
Galimberti, Daniela
Rowe, James B.
Masellis, Mario
Tartaglia, Carmela
Finger, Elizabeth
Vandenberghe, Rik
de 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
van Swieten, John C.
Rohrer, Jonathan D.
author_sort Poos, Jackie M.
collection PubMed
description 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.
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spelling pubmed-81168442021-05-20 Impairment of episodic memory in genetic frontotemporal dementia: A GENFI study Poos, Jackie M. Russell, Lucy L. Peakman, Georgia Bocchetta, Martina Greaves, Caroline V. Jiskoot, Lize C. van der Ende, Emma L. Seelaar, Harro Papma, Janne M. van den Berg, Esther Pijnenburg, Yolande A.L. Borroni, Barbara Sanchez‐Valle, Raquel Moreno, Fermin Laforce, Robert Graff, Caroline Synofzik, Matthias Galimberti, Daniela Rowe, James B. Masellis, Mario Tartaglia, Carmela Finger, Elizabeth Vandenberghe, Rik de 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 van Swieten, John C. Rohrer, Jonathan D. Alzheimers Dement (Amst) Cognitive & Behavioral Assessment 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. John Wiley and Sons Inc. 2021-05-13 /pmc/articles/PMC8116844/ /pubmed/34027016 http://dx.doi.org/10.1002/dad2.12185 Text en © 2021 The Authors. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring published by Wiley Periodicals, LLC on behalf of Alzheimer's Association https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Cognitive & Behavioral Assessment
Poos, Jackie M.
Russell, Lucy L.
Peakman, Georgia
Bocchetta, Martina
Greaves, Caroline V.
Jiskoot, Lize C.
van der Ende, Emma L.
Seelaar, Harro
Papma, Janne M.
van den Berg, Esther
Pijnenburg, Yolande A.L.
Borroni, Barbara
Sanchez‐Valle, Raquel
Moreno, Fermin
Laforce, Robert
Graff, Caroline
Synofzik, Matthias
Galimberti, Daniela
Rowe, James B.
Masellis, Mario
Tartaglia, Carmela
Finger, Elizabeth
Vandenberghe, Rik
de 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
van Swieten, John C.
Rohrer, Jonathan D.
Impairment of episodic memory in genetic frontotemporal dementia: A GENFI study
title Impairment of episodic memory in genetic frontotemporal dementia: A GENFI study
title_full Impairment of episodic memory in genetic frontotemporal dementia: A GENFI study
title_fullStr Impairment of episodic memory in genetic frontotemporal dementia: A GENFI study
title_full_unstemmed Impairment of episodic memory in genetic frontotemporal dementia: A GENFI study
title_short Impairment of episodic memory in genetic frontotemporal dementia: A GENFI study
title_sort impairment of episodic memory in genetic frontotemporal dementia: a genfi study
topic Cognitive & Behavioral Assessment
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8116844/
https://www.ncbi.nlm.nih.gov/pubmed/34027016
http://dx.doi.org/10.1002/dad2.12185
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