Evidence map›Paper›PMID 34273798›Full record

ArticleCortex; a journal devoted to the study of the nervous system and behavior2021

Laughter as a paradigm of socio-emotional signal processing in dementia.

Harri Sivasathiaseelan, Charles R Marshall, Elia Benhamou, Janneke E P van Leeuwen, Rebecca L Bond, Lucy L Russell, Caroline Greaves, Katrina M Moore, Chris J D Hardy, Chris Frost and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Cortex; a journal devoted to the study of the nervous system and behavior, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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

13 authors at 4 institutions in 1 country.

Harri SivasathiaseelanDementia Research Centre, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom. Electronic address: harri.sivasathiaseelan@ucl.ac.uk.
Charles R MarshallDementia Research Centre, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom; Preventive Neurology Unit, Wolfson Institute of Preventive Medicine, Queen Mary University of London, London, United Kingdom.
Elia BenhamouDementia Research Centre, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.
Janneke E P van LeeuwenDementia Research Centre, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.
Rebecca L BondDementia Research Centre, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.
Lucy L RussellDementia Research Centre, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.
Caroline GreavesDementia Research Centre, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.
Katrina M MooreDementia Research Centre, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.
Chris J D HardyDementia Research Centre, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.
Chris FrostDementia Research Centre, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom; Department of Medical Statistics, Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Jonathan D RohrerDementia Research Centre, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.
Sophie K ScottInstitute of Cognitive Neuroscience, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.
Jason D WarrenDementia Research Centre, UCL Queen Square Institute of Neurology, University College London, London, United Kingdom.
UK Dementia Research Institute · GBNational Hospital for Neurology and Neurosurgery · GBQueen Mary University of London · GBUniversity of London · GB

Funding

Medical Research Council MR/M008525/1
6 · The paper itself

Abstract

Laughter is a fundamental communicative signal in our relations with other people and is used to convey a diverse repertoire of social and emotional information. It is therefore potentially a useful probe of impaired socio-emotional signal processing in neurodegenerative diseases. Here we investigated the cognitive and affective processing of laughter in forty-seven patients representing all major syndromes of frontotemporal dementia, a disease spectrum characterised by severe socio-emotional dysfunction (twenty-two with behavioural variant frontotemporal dementia, twelve with semantic variant primary progressive aphasia, thirteen with nonfluent-agrammatic variant primary progressive aphasia), in relation to fifteen patients with typical amnestic Alzheimer's disease and twenty healthy age-matched individuals. We assessed cognitive labelling (identification) and valence rating (affective evaluation) of samples of spontaneous (mirthful and hostile) and volitional (posed) laughter versus two auditory control conditions (a synthetic laughter-like stimulus and spoken numbers). Neuroanatomical associations of laughter processing were assessed using voxel-based morphometry of patients' brain MR images. While all dementia syndromes were associated with impaired identification of laughter subtypes relative to healthy controls, this was significantly more severe overall in frontotemporal dementia than in Alzheimer's disease and particularly in the behavioural and semantic variants, which also showed abnormal affective evaluation of laughter. Over the patient cohort, laughter identification accuracy was correlated with measures of daily-life socio-emotional functioning. Certain striking syndromic signatures emerged, including enhanced liking for hostile laughter in behavioural variant frontotemporal dementia, impaired processing of synthetic laughter in the nonfluent-agrammatic variant (consistent with a generic complex auditory perceptual deficit) and enhanced liking for numbers ('numerophilia') in the semantic variant. Across the patient cohort, overall laughter identification accuracy correlated with regional grey matter in a core network encompassing inferior frontal and cingulo-insular cortices; and more specific correlates of laughter identification accuracy were delineated in cortical regions mediating affective disambiguation (identification of hostile and posed laughter in orbitofrontal cortex) and authenticity (social intent) decoding (identification of mirthful and posed laughter in anteromedial prefrontal cortex) (all p < .05 after correction for multiple voxel-wise comparisons over the whole brain). These findings reveal a rich diversity of cognitive and affective laughter phenotypes in canonical dementia syndromes and suggest that laughter is an informative probe of neural mechanisms underpinning socio-emotional dysfunction in neurodegenerative disease.

Indexed as

Frontotemporal DementiaLaughterNeurodegenerative DiseasesPrimary Progressive Nonfluent AphasiaEmotionsHumansMagnetic Resonance ImagingNeuropsychological TestsAlzheimer's diseaseAuthenticityFrontotemporal dementiaLaughterNumerophiliaProgressive aphasiaSocial cognitionVocal emotion

Identifiers

PMID34273798
PMCPMC8438290
OpenAlexW3177147968

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.