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Social-semantic knowledge in frontotemporal dementia and after anterior temporal lobe resection

Rouse, MA; Halai, AD; Ramanan, S; Rogers, TT; Garrard, P; Patterson, K; Rowe, JB; Lambon Ralph, MA (2024) Social-semantic knowledge in frontotemporal dementia and after anterior temporal lobe resection. BRAIN COMMUNICATIONS, 6 (6). fcae378. ISSN 2632-1297 https://doi.org/10.1093/braincomms/fcae378
SGUL Authors: Garrard, Peter

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Abstract

Degraded semantic memory is a prominent feature of frontotemporal dementia (FTD). It is classically associated with semantic dementia and anterior temporal lobe (ATL) atrophy, but semantic knowledge can also be compromised in behavioural variant FTD. Motivated by understanding behavioural change in FTD, recent research has focused selectively on social-semantic knowledge, with proposals that the right ATL is specialized for social concepts. Previous studies have assessed very different types of social concepts and have not compared performance with that of matched non-social concepts. Consequently, it remains unclear to what extent various social concepts are (i) concurrently impaired in FTD, (ii) distinct from general semantic memory and (iii) differentially supported by the left and right ATL. This study assessed multiple aspects of social-semantic knowledge and general conceptual knowledge across cohorts with ATL damage arising from either neurodegeneration or resection. We assembled a test battery measuring knowledge of multiple types of social concept. Performance was compared with non-social general conceptual knowledge, measured using the Cambridge Semantic Memory Test Battery and other matched non–social-semantic tests. Our trans-diagnostic approach included behavioural variant FTD, semantic dementia and ‘mixed’ intermediate cases to capture the FTD clinical spectrum, as well as age-matched healthy controls. People with unilateral left or right ATL resection for temporal lobe epilepsy were also recruited to assess how selective damage to the left or right ATL impacts social- and non–social-semantic knowledge. Social- and non–social-semantic deficits were severe and highly correlated in FTD. Much milder impairments were found after unilateral ATL resection, with no left versus right differences in social-semantic knowledge or general semantic processing and with only naming showing a greater deficit following left versus right damage. A principal component analysis of all behavioural measures in the FTD cohort extracted three components, interpreted as capturing (i) FTD severity, (ii) semantic memory and (iii) executive function. Social and non-social measures both loaded heavily on the same semantic memory component, and scores on this factor were uniquely associated with bilateral ATL grey matter volume but not with the degree of ATL asymmetry. Together, these findings demonstrate that both social- and non–social-semantic knowledge degrade in FTD (semantic dementia and behavioural variant FTD) following bilateral ATL atrophy. We propose that social-semantic knowledge is part of a broader conceptual system underpinned by a bilaterally implemented, functionally unitary semantic hub in the ATLs. Our results also highlight the value of a trans-diagnostic approach for investigating the neuroanatomical underpinnings of cognitive deficits in FTD.

Item Type: Article
Additional Information: © The Author(s) 2024. Published by Oxford University Press on behalf of the Guarantors of Brain. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords: behavioural variant frontotemporal dementia, semantic dementia, social concept, temporal lobe epilepsy, trans-diagnostic
SGUL Research Institute / Research Centre: Academic Structure > Neuroscience & Cell Biology Research Institute
Academic Structure > Neuroscience & Cell Biology Research Institute > Neurological Disorders & Imaging
Journal or Publication Title: BRAIN COMMUNICATIONS
ISSN: 2632-1297
Dates:
DateEvent
28 October 2024Published
25 October 2024Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
SUAG/096 G116768Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MR/V031481/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MC_UU_00030/14Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MR/T033371,1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
220258Wellcome Trusthttp://dx.doi.org/10.13039/100004440
NIHR203312NIHR Cambridge Biomedical Research Centrehttp://dx.doi.org/10.13039/501100018956
MR/R023883/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MC_UU_00005/18Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
Web of Science ID: WOS:001350669600001
URI: https://openaccess.sgul.ac.uk/id/eprint/116958
Publisher's version: https://doi.org/10.1093/braincomms/fcae378

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