Evidence map›Paper›PMID 37705680›Full record

ArticleBrain communications2023

Elevated representational similarity of voluntary action and inhibition in Tourette syndrome.

Charlotte L Rae, Petar Raykov, Eleanor M Ambridge, Lincoln J Colling, Cassandra D Gould van Praag, Samira Bouyagoub, Liliana Polanski, Dennis E O Larsson, Hugo D Critchley

Abstract read
In one paragraph

Article in Brain communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  4. 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

9 authors.

Charlotte L RaeSchool of Psychology, University of Sussex, Brighton BN1 9QH, UK.ORCID https://orcid.org/0000-0002-4503-4971
Petar RaykovSchool of Psychology, University of Sussex, Brighton BN1 9QH, UK.
Eleanor M AmbridgeSchool of Psychology, University of Sussex, Brighton BN1 9QH, UK.
Lincoln J CollingSchool of Psychology, University of Sussex, Brighton BN1 9QH, UK.
Cassandra D Gould van PraagWellcome Centre for Integrative Neuroimaging, University of Oxford, Oxford OX3 7JX, UK.
Samira BouyagoubDepartment of Neuroscience, Brighton & Sussex Medical School, Brighton BN1 9RY, UK.
Liliana PolanskiCenter for Lifespan Psychology, Max Planck Institute for Human Development, Berlin 14195, Germany.
Dennis E O LarssonSchool of Psychology, University of Sussex, Brighton BN1 9QH, UK.ORCID https://orcid.org/0000-0002-8931-6065
Hugo D CritchleyDepartment of Neuroscience, Brighton & Sussex Medical School, Brighton BN1 9RY, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many people with Tourette syndrome are able to volitionally suppress tics, under certain circumstances. To understand better the neural mechanisms that underlie this ability, we used functional magnetic resonance neuroimaging to track regional brain activity during performance of an intentional inhibition task. On some trials, Tourette syndrome and comparison participants internally chose to make or withhold a motor action (a button press), while on other trials, they followed 'Go' and 'NoGo' instructions to make or withhold the same action. Using representational similarity analysis, a functional magnetic resonance neuroimaging multivariate pattern analysis technique, we assessed how Tourette syndrome and comparison participants differed in neural activity when choosing to make or to withhold an action, relative to externally cued responses on Go and NoGo trials. Analyses were pre-registered, and the data and code are publicly available. We considered similarity of action representations within regions implicated as critical to motor action release or inhibition and to symptom expression in Tourette syndrome, namely the pre-supplementary motor area, inferior frontal gyrus, insula, caudate nucleus and primary motor cortex. Strikingly, in the Tourette syndrome compared to the comparison group, neural activity within the pre-supplementary motor area displayed greater representational similarity across all action types. Within the pre-supplementary motor area, there was lower response-specific differentiation of activity relating to action and inhibition plans and to internally chosen and externally cued actions, implicating the region as a functional nexus in the symptomatology of Tourette syndrome. Correspondingly, patients with Tourette syndrome may experience volitional tic suppression as an effortful and tiring process because, at the top of the putative motor decision hierarchy, activity within the population of neurons facilitating action is overly similar to activity within the population of neurons promoting inhibition. However, not all pre-supplementary motor area group differences survived correction for multiple comparisons. Group differences in representational similarity were also present in the primary motor cortex. Here, representations of internally chosen and externally cued inhibition were more differentiated in the Tourette syndrome group than in the comparison group, potentially a consequence of a weaker voluntary capacity earlier in the motor hierarchy to suppress actions proactively. Tic severity and premonitory sensations correlated with primary motor cortex and caudate nucleus representational similarity, but these effects did not survive correction for multiple comparisons. In summary, more rigid pre-supplementary motor area neural coding across action categories may constitute a central feature of Tourette syndrome, which can account for patients' experience of 'unvoluntary' tics and effortful tic suppression.

Indexed as

basal gangliaintentional inhibitionpre-supplementary motor areaTourette syndromevoluntary action

Identifiers

PMID37705680
PMCPMC10497185

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Registered trials

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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.