Evidence map›Paper›PMID 39513090›Full record

ArticleBrain communications2024

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

Matthew A Rouse, Ajay D Halai, Siddharth Ramanan, Timothy T Rogers, Peter Garrard, Karalyn Patterson, James B Rowe, Matthew A Lambon Ralph

Abstract read
In one paragraph

Article in Brain communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. The Role of the Anterior Temporal Lobe in Reading: An HD-tDCS Study.Neurobiology of language (Cambridge, Mass.) · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Matthew A RouseMRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge CB2 7EF, UK.ORCID https://orcid.org/0000-0002-3157-4301
Ajay D HalaiMRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge CB2 7EF, UK.ORCID https://orcid.org/0000-0003-1725-7948
Siddharth RamananMRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge CB2 7EF, UK.
Timothy T RogersDepartment of Psychology, University of Wisconsin-Madison, Madison, WI 53706, USA.
Peter GarrardMolecular and Clinical Sciences Research Institute, St George's, University of London, London SW17 0RE, UK.ORCID https://orcid.org/0000-0001-8268-9718
Karalyn PattersonMRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge CB2 7EF, UK.ORCID https://orcid.org/0000-0003-1927-7424
James B RoweMRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge CB2 7EF, UK.
Matthew A Lambon RalphMRC Cognition and Brain Sciences Unit, University of Cambridge, Cambridge CB2 7EF, UK.ORCID https://orcid.org/0000-0001-5907-2488

Funding

Wellcome Trust
6 · The paper itself

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.

Indexed as

behavioural variant frontotemporal dementiasemantic dementiasocial concepttemporal lobe epilepsytrans-diagnostic

Identifiers

PMID39513090
PMCPMC11542483

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.