Evidence map›Paper›PMID 34439617›Full record

ArticleBrain sciences2021

Anhedonia in Semantic Dementia-Exploring Right Hemispheric Contributions to the Loss of Pleasure.

Siobhán R Shaw, Hashim El-Omar, Siddharth Ramanan, Olivier Piguet, Rebekah M Ahmed, Alexis E Whitton, Muireann Irish

Abstract read
In one paragraph

Article in Brain sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

14 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Observational
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Anhedonia in Neurodegenerative Diseases.Current topics in behavioral neurosciences · 2022
    Review
  12. Article
  13. Article
  14. 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

7 authors.

Siobhán R ShawBrain and Mind Centre, The University of Sydney, 94 Mallett Street, Sydney, NSW 2050, Australia.
Hashim El-OmarBrain and Mind Centre, The University of Sydney, 94 Mallett Street, Sydney, NSW 2050, Australia.ORCID 0000-0003-2304-7277
Siddharth RamananBrain and Mind Centre, The University of Sydney, 94 Mallett Street, Sydney, NSW 2050, Australia.ORCID 0000-0002-8591-042X
Olivier PiguetBrain and Mind Centre, The University of Sydney, 94 Mallett Street, Sydney, NSW 2050, Australia.ORCID 0000-0002-6696-1440
Rebekah M AhmedBrain and Mind Centre, The University of Sydney, 94 Mallett Street, Sydney, NSW 2050, Australia.
Alexis E WhittonBlack Dog Institute, University of New South Wales, Sydney, NSW 2031, Australia.ORCID 0000-0002-7944-2172
Muireann IrishBrain and Mind Centre, The University of Sydney, 94 Mallett Street, Sydney, NSW 2050, Australia.ORCID 0000-0002-4950-8169

Funding

Australian Research Council FT160100096Centre of Excellence in Cognition and its Disorders, Australian Research Council CE11000102National Health and Medical Research Council 1103258National Health and Medical Research Council 1110773National Health and Medical Research Council Dementia Research Team Grant 1095127National Health and Medical Research Council Program Grant 1132524National Health and Medical Research Council Project Grant 1121791
6 · The paper itself

Abstract

Semantic dementia (SD) is a younger-onset neurodegenerative disease characterised by progressive deterioration of the semantic knowledge base in the context of predominantly left-lateralised anterior temporal lobe (ATL) atrophy. Mounting evidence indicates the emergence of florid socioemotional changes in SD as atrophy encroaches into right temporal regions. How lateralisation of temporal lobe pathology impacts the hedonic experience in SD remains largely unknown yet has important implications for understanding socioemotional and functional impairments in this syndrome. Here, we explored how lateralisation of temporal lobe atrophy impacts anhedonia severity on the Snaith-Hamilton Pleasure Scale in 28 SD patients presenting with variable right- (SD-R) and left-predominant (SD-L) profiles of temporal lobe atrophy compared to that of 30 participants with Alzheimer's disease and 30 healthy older Control participants. Relative to Controls, SD-R but not SD-L or Alzheimer's patients showed clinically significant anhedonia, representing a clear departure from premorbid levels. Overall, anhedonia was more strongly associated with functional impairment on the Frontotemporal Dementia Functional Rating Scale and motivational changes on the Cambridge Behavioural Inventory in SD than in Alzheimer's disease patients. Voxel-based morphometry analyses revealed that anhedonia severity correlated with reduced grey matter intensity in a restricted set of regions centred on right orbitofrontal and temporopolar cortices, bilateral posterior temporal cortices, as well as the anterior cingulate gyrus and parahippocampal gyrus, bilaterally. Finally, regression and mediation analysis indicated a unique role for right temporal lobe structures in modulating anhedonia in SD. Our findings suggest that degeneration of predominantly right-hemisphere structures deleteriously impacts the capacity to experience pleasure in SD. These findings offer important insights into hemispheric lateralisation of motivational disturbances in dementia and suggest that anhedonia may emerge at different timescales in the SD disease trajectory depending on the integrity of the right hemisphere.

Indexed as

Alzheimer’s diseasedepressionfrontotemporal dementiamotivationneuroimagingstriatum

Identifiers

PMID34439617
PMCPMC8392684

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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.