Evidence map›Paper›PMID 42842340›Full record

ArticlePsychophysiology2026

Altered Interoceptive Predictive Coding in Functional Neurological Disorders.

Natascha Stoffel, Michaël Mouthon, Andria Pelentritou, Laure von der Weid, Cristina Concetti, Marzia De Lucia, Selma Aybek

Abstract read
In one paragraph

Article in Psychophysiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Natascha StoffelDepartment of Neurology, Faculty of Science and Medicine, University of Fribourg, Fribourg, Switzerland.ORCID https://orcid.org/0009-0000-4198-4921
Michaël MouthonDepartment of Neurology, Faculty of Science and Medicine, University of Fribourg, Fribourg, Switzerland.
Andria PelentritouBrain-Body and Consciousness Laboratory, Department of Clinical Neuroscience, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.ORCID https://orcid.org/0009-0007-1323-2803
Laure von der WeidDepartment of Neurology, Faculty of Science and Medicine, University of Fribourg, Fribourg, Switzerland.
Cristina ConcettiDepartment of Neurology, Faculty of Science and Medicine, University of Fribourg, Fribourg, Switzerland.ORCID https://orcid.org/0000-0002-9755-3298
Marzia De LuciaBrain-Body and Consciousness Laboratory, Department of Clinical Neuroscience, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.ORCID https://orcid.org/0000-0001-8792-7885
Selma AybekDepartment of Neurology, Faculty of Science and Medicine, University of Fribourg, Fribourg, Switzerland.ORCID https://orcid.org/0000-0002-7877-6760

Funding

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung PP00P3_176985
6 · The paper itself

Abstract

Interoception, the processing of internal bodily signals, has been linked to the pathophysiology of Functional Neurological Disorder (FND), along with the theoretical concept of altered predictive coding (PC). FND symptoms such as sensory-motor dysfunction may arise from disrupted integration of sensory input and predictions. However, PC in the modality of interoception has not yet been investigated in FND. Using a PC paradigm, the cardio-audio synchronization task measured electrophysiological responses to the heartbeat during omitted sounds that were temporally locked to the heartbeat (synchronous condition) or not (asynchronous control condition). Patients with mixed FND symptoms (N = 36) were compared to sex- and age-matched healthy controls (HC: N = 42) by contrasting synchronous and asynchronous heartbeat-evoked potentials during omissions using cluster-based permutation statistics. We further tested associations with self-reported interoceptive variables and assessed whole-scalp main and interaction effects in global field power (GFP) and topography. Patients with FND showed no cluster-level differences between conditions, whereas we identified a central cluster difference in HCs. The interoceptive-specific contrast (synch-asynch difference waves) differed between groups and correlated with interoceptive self-report but only when tested across groups (r = -0.33, p = 0.012). In this paradigm, group-by-condition interactions in topography identified the insula as the most probable source of differences. These interactions occurred before those identified in GFP analyses, suggesting that differential networks emerge first, followed by changes in overall activity strength. These results indicate that patients with FND use different neural mechanisms for interoceptive PC (i.e., precision-weighted prediction errors in interoception-guided predictions) than HCs. Patients with FND showed no difference in interoceptive PC, suggesting a dysfunctional interoceptive system. Together, these findings suggest that interoceptive-cued regularity processing in FND is characterized by altered early network recruitment, followed by differences in overall signal strength, potentially reflecting a disrupted progression of interoceptive PC.

Indexed as

Cerebral CortexEvoked PotentialsHeart RateInteroceptionNervous System DiseasesAdultElectroencephalographyFemaleHumansMaleMiddle AgedYoung Adultconversion disorderEEGheartbeat‐evoked potentialsInteroceptionpredictive coding

Identifiers

PMID42842340
PMCPMC13644901

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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.