Evidence map›Paper›PMID 41708484›Full record

Trial reportHuman brain mapping2026

Emotion Processing in Schizophrenia: Insights From a Brain Imaging Study Comparing Patients, Siblings, and Healthy Controls.

Anna M Fiorito, Ayman Kheireddine, Hyemin Han, Colas Morel-Prieur, Nicolas Oriol, Fabien C Schneider, Guillaume Sescousse, Eric Fakra

Registry-linked trialAbstract readClinical Trial
In one paragraph

Trial report in Human brain mapping, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02834208 (Neurofunctional Basis of Emotion Processing), which is not on this 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

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.

NCT02834208 naunknown statusnot on this map

Neurofunctional Basis of Emotion Processing: Clinical, Genetic, Biological and Imaging Study in Patients With Schizophrenia and Healthy Relatives of Patients in Comparison With a Control Group

TypeinterventionalSponsorAssistance Publique Hopitaux De MarseilleRan2015 to 2019Enrolled105ConditionsSchizophreniaArmsMRI (Magnetic resonance imaging), Polymorphism (SNP in DNA), quantitative measures of mRNA, Neuropsychological assessment
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

8 authors.

Anna M FioritoUniversité Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, PSYR2, Bron, France.ORCID https://orcid.org/0000-0001-9339-3541
Ayman KheireddineDepartment of Psychiatry, University Hospital of Saint-Etienne, Saint-Etienne, France.
Hyemin HanEducational Psychology Program, University of Alabama, Tuscaloosa, Alabama, USA.
Colas Morel-PrieurDepartment of Psychiatry, University Hospital of Saint-Etienne, Saint-Etienne, France.
Nicolas OriolDepartment of Psychiatry, University Hospital of Saint-Etienne, Saint-Etienne, France.
Fabien C SchneiderUniversité Jean Monnet Saint-Etienne, CHU Saint-Etienne, Unité de Recherche TAPE, Saint-Etienne, France.
Guillaume SescousseUniversité Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, PSYR2, Bron, France.ORCID https://orcid.org/0000-0002-8556-3755
Eric FakraUniversité Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, PSYR2, Bron, France.

Funding

Agence Nationale de la Recherche ANR-19-CE37-0012-01Centre Hospitalier Le VinatierFondation de FranceFondation NeurodisFondation NRJ-Institut de FranceFondation Pierre Deniker pour la Recherche et la Prévention en Santé MentaleUniversity Hospital of Saint-Etienne
6 · The paper itself

Abstract

Abnormal facial emotion recognition has been proposed as a potential endophenotype for schizophrenia, as both patients with schizophrenia and their healthy relatives show difficulties in recognizing negative facial emotions. In psychiatric disorders, brain functioning is considered highly informative for endophenotype research. However, recent studies have raised questions about our current understanding of the neural correlates of emotion recognition across the schizophrenia spectrum, pointing out two major limitations in previous research. First, individual fMRI studies and meta-analyses have predominantly used neutral stimuli as a comparator in emotional tasks. Yet, recent evidence indicates that neutral stimuli are not perceived as truly neutral by patients with schizophrenia or their first-degree relatives, thereby calling into question the interpretability of earlier findings. Second, few studies have explored brain connectivity in response to negative emotional faces in healthy relatives of patients, even though emotions are processed by a complex network of interconnected brain structures. This study aims to investigate the neural mechanisms underlying emotion processing in patients with schizophrenia and their siblings, focusing on brain activation and functional connectivity during the perception of negatively valenced facial expressions. We employed a more ecologically valid task compared with previous studies, incorporating emotional faces within an emotionally charged context. By employing a well-matched control condition and examining connectivity patterns within emotion-processing networks, we seek to address the limitations of prior research. 118 participants (37 patients with schizophrenia, 39 siblings, and 42 healthy controls) underwent functional magnetic resonance imaging (fMRI) scanning while performing an emotional task involving negatively valenced faces and control conditions. Behavioral performance was assessed using the Balanced Integration Score (BIS) to evaluate speed-accuracy tradeoffs. fMRI data were analyzed for brain activation, using a complementary approach based on frequentist and Bayesian statistics, as well as for functional connectivity, using generalized psychophysiological interaction (gPPI) analysis with the right and left amygdala as seed regions. Behavioral analyses revealed significant group differences, with both patients and their siblings displaying lower BIS scores compared with controls. Exploratory between-group fMRI analyses revealed that, compared with controls, siblings exhibited decreased brain responses to negative faces in a cluster encompassing the right superior temporal gyrus and the right postcentral gyrus. Bayesian analyses showed that, as compared with controls, patients seem to display similarly impaired activation in the right postcentral gyrus. In most of the rest of the brain, including the amygdala, Bayesian analyses indicated an absence of group differences for both patients and siblings compared with controls. Functional connectivity analyses revealed that siblings had stronger task-related connectivity between the right amygdala and the right cuneus compared with controls. Our findings provide evidence that while the amygdala appears to respond to negative faces similarly among controls, siblings, and patients, an endophenotypic pattern may be present in the right postcentral gyrus. Furthermore, these results suggest that activation-based analyses may not fully capture the neural abnormalities associated with emotion processing in relatives of patients with schizophrenia. We hypothesize that the increased connectivity between the right amygdala and the right cuneus may reflect a compensatory mechanism in siblings. CLINICAL REGISTRATION: https://clinicaltrials.gov/study/NCT02834208?term=schizoimagen&rank=1.

Indexed as

BrainConnectomeEmotionsFacial RecognitionSchizophreniaSchizophrenic PsychologySiblingsAdultBrain MappingEndophenotypesFacial ExpressionFemaleHumansMagnetic Resonance ImagingMaleYoung AdultconnectivityemotionendophenotypefMRIschizophreniasiblings

Identifiers

PMID41708484
PMCPMC12916247

What Socratic holds

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LicenceCC BY
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Registered trials

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 Socratic graph.