Evidence map›Paper›PMID 42141758›Full record

ArticleThe European journal of neuroscience2026

Conscious Tactile Perception Depends on Early Processing in Primary Somatosensory Cortex.

Louisa Gwynne, Luigi Tamè

Abstract read
In one paragraph

Article in The European journal of neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

2 authors.

Louisa GwynneSchool of Psychology, University of Kent, Canterbury, UK.ORCID 0009-0009-1594-8420
Luigi TamèSchool of Psychology, University of Kent, Canterbury, UK.

Funding

Economic and Social Research Council ES/P00072X/1
6 · The paper itself

Abstract

The primary somatosensory cortex (S1) has long been implicated in tactile perception, yet its precise role in conscious tactile detection remains uncertain. The current study investigated the causal and time-specific involvement of S1 in tactile detection using single-pulse transcranial magnetic stimulation (spTMS). In two experiments, spTMS was applied over contralateral S1, an active control site (inferior parietal lobe; IPL), or under a sham condition at short (25 and 75 ms; Experiment 1) or longer (130 ms; Experiment 2) intervals following electrotactile stimulation of the finger. Participants performed a go/no-go detection task at sensory threshold. In Experiment 1, tactile sensitivity was significantly reduced following early S1 stimulation compared with both active control and sham conditions. In contrast, no such effect was observed at a later timepoint in Experiment 2. Self-reported TMS-related distraction ratings did not account for the observed sensitivity differences, suggesting sensitivity-specific modulation by early TMS rather than general task disruption. Together, these findings support a causal role for early S1 activity in conscious tactile detection. We propose that disruption at this early stage impairs initial encoding of tactile input, thereby attenuating subsequent perceptual awareness. Overall, the results underscore the critical contribution of S1 in conscious tactile detection and are compatible with recent accounts in which conscious tactile perception emerges from processing within a distributed neural network.

Indexed as

ConsciousnessSomatosensory CortexTouch PerceptionAdultFemaleHumansMaleSensory ThresholdsTranscranial Magnetic StimulationYoung Adultconscious perceptionsomatosensory cortextactile detectiontemporal processingtranscranial magnetic stimulation

Identifiers

PMID42141758
PMCPMC13179477

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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.