Evidence map›Paper›PMID 35733166›Full record

ArticleOrphanet journal of rare diseases2022

Dissociation of early and late face-related processes in autism spectrum disorder and Williams syndrome.

Alice Gomez, Guillaume Lio, Manuela Costa, Angela Sirigu, Caroline Demily

Open access · goldAbstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2022. 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
0.4field-weighted citation impact, top 42% of its field
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, 3 citations in OpenAlex.

  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

5 authors at 2 institutions in 3 countries.

Alice Gomez *Institut Des Sciences, Cognitives Marc Jeannerod, Centre National de La Recherche Scientifique, 67 boulevard Pinel, 69500, Bron, France. alice.gomez@univ-lyon1.fr.ORCID 0000-0003-4804-4419
Guillaume Lio *Institut Des Sciences, Cognitives Marc Jeannerod, Centre National de La Recherche Scientifique, 67 boulevard Pinel, 69500, Bron, France.
Manuela CostaInstitut Des Sciences, Cognitives Marc Jeannerod, Centre National de La Recherche Scientifique, 67 boulevard Pinel, 69500, Bron, France.
Angela Sirigu *Institut Des Sciences, Cognitives Marc Jeannerod, Centre National de La Recherche Scientifique, 67 boulevard Pinel, 69500, Bron, France.
Caroline DemilyInstitut Des Sciences, Cognitives Marc Jeannerod, Centre National de La Recherche Scientifique, 67 boulevard Pinel, 69500, Bron, France. Caroline.DEMILY@ch-le-vinatier.fr.
Université Claude Bernard Lyon 1 · FRInstitut des Sciences Cognitives · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWilliams syndrome (WS) and Autism Spectrum Disorders (ASD) are neurodevelopmental conditions associated with atypical but opposite face-to-face interactions patterns: WS patients overly stare at others, ASD individuals escape eye contact. Whether these behaviors result from dissociable visual processes within the occipito-temporal pathways is unknown. Using high-density electroencephalography, multivariate signal processing algorithms and a protocol designed to identify and extract evoked activities sensitive to facial cues, we investigated how WS (N = 14), ASD (N = 14) and neurotypical subjects (N = 14) decode the information content of a face stimulus.

resultsWe found two neural components in neurotypical participants, both strongest when the eye region was projected onto the subject's fovea, simulating a direct eye contact situation, and weakest over more distant regions, reaching a minimum when the focused region was outside the stimulus face. The first component peaks at 170 ms, an early signal known to be implicated in low-level face features. The second is identified later, 260 ms post-stimulus onset and is implicated in decoding salient face social cues. Remarkably, both components were found distinctly impaired and preserved in WS and ASD. In WS, we could weakly decode the 170 ms signal based on our regressor relative to facial features, probably due to their relatively poor ability to process faces' morphology, while the late 260 ms component was highly significant. The reverse pattern was observed in ASD participants who showed neurotypical like early 170 ms evoked activity but impaired late evoked 260 ms signal.

conclusionsOur study reveals a dissociation between WS and ASD patients and points at different neural origins for their social impairments.

Indexed as

Autism Spectrum DisorderNeurodevelopmental DisordersWilliams SyndromeElectroencephalographyHumansEye sensitiveFacial featuresFusiform face areaSocial brainSuperior Temporal Sulcus

Identifiers

PMID35733166
PMCPMC9215067
OpenAlexW4283363075

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.