TY - JOUR
T1 - Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort
AU - Genetic FTD Initiative (GENFI)
AU - Russell, Lucy L.
AU - Greaves, Caroline V.
AU - Bocchetta, Martina
AU - Nicholas, Jennifer
AU - Convery, Rhian S.
AU - Moore, Katrina
AU - Cash, David M.
AU - van Swieten, John
AU - Jiskoot, Lize
AU - Moreno, Fermin
AU - Sanchez-Valle, Raquel
AU - Borroni, Barbara
AU - Laforce, Robert
AU - Masellis, Mario
AU - Tartaglia, Maria Carmela
AU - Graff, Caroline
AU - Rotondo, Emanuela
AU - Galimberti, Daniela
AU - Rowe, James B.
AU - Finger, Elizabeth
AU - Synofzik, Matthis
AU - Vandenberghe, Rik
AU - de Mendonça, Alexandre
AU - Tagliavini, Fabrizio
AU - Santana, Isabel
AU - Ducharme, Simon
AU - Gerhard, Alex
AU - Levin, Johannes
AU - Danek, Adrian
AU - Otto, Markus
AU - Warren, Jason D.
AU - Rohrer, Jonathan D.
AU - Rossor, Martin N.
AU - Fox, Nick C.
AU - Woollacott, Ione O.C.
AU - Shafei, Rachelle
AU - Heller, Carolin
AU - Guerreiro, Rita
AU - Bras, Jose
AU - Mead, Simon
AU - Meeter, Lieke
AU - Panman, Jessica
AU - Papma, Janne
AU - Poos, Jackie
AU - van Minkelen, Rick
AU - Pijnenburg, Yolanda
AU - Barandiaran, Myriam
AU - Indakoetxea, Begoña
AU - Thompson, Paul
AU - Langheinrich, Tobias
N1 - Funding Information:
We thank the research participants for their contribution to the study. The Dementia Research Centre is supported by Alzheimer's Research UK, Alzheimer's Society, Brain Research UK, and The Wolfson Foundation. This work was supported by the NIHR UCLH Biomedical Research Centre, the Leonard Wolfson Experimental Neurology Centre (LWENC) Clinical Research Facility, and the UK Dementia Research Institute, which receives its funding from UK DRI Ltd. , funded by the UK Medical Research Council , Alzheimer's Society and Alzheimer's Research UK . JDR is supported by an MRC Clinician Scientist Fellowship ( MR/M008525/1 ) and has received funding from the NIHR Rare Disease Translational Research Collaboration ( BRC149/NS/MH ), the Bluefield Project and the Association for Frontotemporal Degeneration. This work was also supported by the MRC UK GENFI grant ( MR/M023664/1 ). MB is supported by a Fellowship award from the Alzheimer's Society, UK (AS-JF-19a-004-517). Several authors of this publication are members of the European Reference Network for Rare Neurological Diseases - Project ID No 739510. RS-V is supported by an Alzheimer’s Research UK Clinical Research Training Fellowship ( ARUK-CRF2017B-2 ). JCVS was supported by the Dioraphte Foundation grant 09-02-03-00 , the Association for Frontotemporal Dementias Research Grant 2009 , The Netherlands Organization for Scientific Research (NWO) grant HCMI 056-13-018 , ZonMw Memorabel (Deltaplan Dementie, project number 733 051 042), Alzheimer Nederland and the Bluefield project. CG received funding from JPND-Prefrontals VR Dnr 529-2014-7504 , VR 2015-02926 and 2018-02754 , the Swedish FTD Initiative-Schörling Foundation, Alzheimer Foundation, Brain Foundation and Stockholm County Council ALF. DG received support from the EU Joint Programme - Neurodegenerative Disease Research (JPND) and the Italian Ministry of Health (PreFrontALS) grant 733051042. RS-V has received funding from Fundació Marató de TV3 , Spain (grant no. 20143810 ). FM received funding from the Tau Consortium and the Center for Networked Biomedical Research on Neurodegenerative Disease (CIBERNED). JBR has received funding from the Wellcome Trust ( 103838 ) and the National Institute for Health Research (NIHR) Bambridge Biomedical Research Centre. MO has received funding from BMBF (FTLDc) . MM has received funding from a Canadian Institute of Health Research operating grant and the Weston Brain institute and Ontario Brain Institute . RV has received funding from the Mady Browaeys Fund for Research into Frontotemporal Dementia. EF has received funding from a Canadian Institute of Health Research grant # 327387 .
Publisher Copyright:
© 2020 The Author(s)
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/12/1
Y1 - 2020/12/1
N2 - A key symptom of frontotemporal dementia (FTD) is difficulty interacting socially with others. Social cognition problems in FTD include impaired emotion processing and theory of mind difficulties, and whilst these have been studied extensively in sporadic FTD, few studies have investigated them in familial FTD. Facial Emotion Recognition (FER) and Faux Pas (FP) recognition tests were used to study social cognition within the Genetic Frontotemporal Dementia Initiative (GENFI), a large familial FTD cohort of C9orf72, GRN, and MAPT mutation carriers. 627 participants undertook at least one of the tasks, and were separated into mutation-negative healthy controls, presymptomatic mutation carriers (split into early and late groups) and symptomatic mutation carriers. Groups were compared using a linear regression model with bootstrapping, adjusting for age, sex, education, and for the FP recognition test, language. Neural correlates of social cognition deficits were explored using a voxel-based morphometry (VBM) study. All three of the symptomatic genetic groups were impaired on both tasks with no significant difference between them. However, prior to onset, only the late presymptomatic C9orf72 mutation carriers on the FER test were impaired compared to the control group, with a subanalysis showing differences particularly in fear and sadness. The VBM analysis revealed that impaired social cognition was mainly associated with a left hemisphere predominant network of regions involving particularly the striatum, orbitofrontal cortex and insula, and to a lesser extent the inferomedial temporal lobe and other areas of the frontal lobe. In conclusion, theory of mind and emotion processing abilities are impaired in familial FTD, with early changes occurring prior to symptom onset in C9orf72 presymptomatic mutation carriers. Future work should investigate how performance changes over time, in order to gain a clearer insight into social cognitive impairment over the course of the disease.
AB - A key symptom of frontotemporal dementia (FTD) is difficulty interacting socially with others. Social cognition problems in FTD include impaired emotion processing and theory of mind difficulties, and whilst these have been studied extensively in sporadic FTD, few studies have investigated them in familial FTD. Facial Emotion Recognition (FER) and Faux Pas (FP) recognition tests were used to study social cognition within the Genetic Frontotemporal Dementia Initiative (GENFI), a large familial FTD cohort of C9orf72, GRN, and MAPT mutation carriers. 627 participants undertook at least one of the tasks, and were separated into mutation-negative healthy controls, presymptomatic mutation carriers (split into early and late groups) and symptomatic mutation carriers. Groups were compared using a linear regression model with bootstrapping, adjusting for age, sex, education, and for the FP recognition test, language. Neural correlates of social cognition deficits were explored using a voxel-based morphometry (VBM) study. All three of the symptomatic genetic groups were impaired on both tasks with no significant difference between them. However, prior to onset, only the late presymptomatic C9orf72 mutation carriers on the FER test were impaired compared to the control group, with a subanalysis showing differences particularly in fear and sadness. The VBM analysis revealed that impaired social cognition was mainly associated with a left hemisphere predominant network of regions involving particularly the striatum, orbitofrontal cortex and insula, and to a lesser extent the inferomedial temporal lobe and other areas of the frontal lobe. In conclusion, theory of mind and emotion processing abilities are impaired in familial FTD, with early changes occurring prior to symptom onset in C9orf72 presymptomatic mutation carriers. Future work should investigate how performance changes over time, in order to gain a clearer insight into social cognitive impairment over the course of the disease.
KW - C9orf72
KW - Emotion processing
KW - Facial emotion recognition
KW - Faux pas
KW - Frontotemporal dementia
KW - MAPT
KW - Progranulin
KW - Theory of mind
U2 - 10.1016/j.cortex.2020.08.023
DO - 10.1016/j.cortex.2020.08.023
M3 - Article
C2 - 33221702
AN - SCOPUS:85096395411
SN - 0010-9452
VL - 133
SP - 384
EP - 398
JO - Cortex
JF - Cortex
ER -