Evidence map›Paper›PMID 39709442›Full record

Trial reportMolecular autism2024

Impact of chronic intranasal oxytocin administration on face expression processing in autistic children: a randomized controlled trial using fMRI.

Matthijs Moerkerke, Nicky Daniels, Stephanie Van der Donck, Tiffany Tang, Jellina Prinsen, Elahe' Yargholi, Jean Steyaert, Kaat Alaerts, Bart Boets

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Molecular autism, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Neuropeptidergic systems in psychiatric disorders.Frontiers in endocrinology · 2025
    Review
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.

Matthijs Moerkerke *Department of Neurosciences, Center for Developmental Psychiatry, KU Leuven, Leuven, Belgium. matthijs.moerkerke@kuleuven.be.
Nicky Daniels *Leuven Autism Research (LAuRes), KU Leuven, Leuven, Belgium.
Stephanie Van der DonckDepartment of Neurosciences, Center for Developmental Psychiatry, KU Leuven, Leuven, Belgium.
Tiffany TangDepartment of Neurosciences, Center for Developmental Psychiatry, KU Leuven, Leuven, Belgium.
Jellina PrinsenLeuven Autism Research (LAuRes), KU Leuven, Leuven, Belgium.
Elahe' YargholiDepartment of Brain and Cognition, Faculty of Psychology & Educational Sciences, KU Leuven, Leuven, Belgium.
Jean SteyaertDepartment of Neurosciences, Center for Developmental Psychiatry, KU Leuven, Leuven, Belgium.
Kaat Alaerts *Leuven Autism Research (LAuRes), KU Leuven, Leuven, Belgium.
Bart Boets *Department of Neurosciences, Center for Developmental Psychiatry, KU Leuven, Leuven, Belgium.

Funding

Excellence of Science grant EOS; G0E8718N; HUMVISCATFonds Wetenschappelijk Onderzoek FWO; 1257621NFonds Wetenschappelijk Onderzoek FWO; 12C9723NFonds Wetenschappelijk Onderzoek FWO-TBM T001821NKoning Boudewijnstichting 2019-J1811190-212989KU Leuven C14/17/102KU Leuven PDM/20/170KU Leuven PDM/22/065
6 · The paper itself

Abstract

backgroundDifficulties with (non-verbal) social communication, including facial expression processing, constitute a hallmark of autism. Intranasal administration of oxytocin has been considered a potential therapeutic option for improving social difficulties in autism, either by enhancing the salience of social cues or by reducing the social stress and anxiety experienced in social encounters.

methodsWe recorded fMRI brain activity while presenting neutral, fearful and scrambled faces, to compare the neural face processing signature of autistic children (n = 58) with that of matched non-autistic controls (n = 38). Next, in the autistic children group, we implemented this fMRI face processing task in a double-blind, placebo-controlled, multiple-dose oxytocin clinical trial, to evaluate the impact of four-week repeated oxytocin administration (24 IU daily dose) on brain activity in face processing regions.

resultsNo significant diagnostic-group differences were identified between autistic versus non-autistic children with regard to neural face processing. Furthermore, no significant treatment effects were found in the oxytocin clinical trial. However, exploratory analyses (uncorrected for multiple comparisons) demonstrated decreases in brain activity in the left superior temporal sulcus (STS) and inferior frontal region in the oxytocin compared to the placebo group, and change-from-baseline analyses in the oxytocin group revealed significantly reduced neural activity in the core face-processing network (STS, inferior occipital, and posterior fusiform), as well as in amygdala and inferior frontal region.

conclusionThese findings suggest an attenuating effect of multiple-dose oxytocin administration on neural face processing, potentially supporting the anxiolytic account of oxytocin.

Indexed as

Administration, IntranasalAutistic DisorderFacial ExpressionMagnetic Resonance ImagingOxytocinAdolescentBrainChildDouble-Blind MethodFacial RecognitionFemaleHumansMaleOxytocinAutismChronic oxytocin administrationExpressive facesFace processingfMRI

Identifiers

PMID39709442
PMCPMC11662540

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.