Evidence map›Paper›PMID 34899412›Full record

ArticleFrontiers in psychiatry2021

Neural Correlates of Infant Face Processing and Later Emerging Autism Symptoms in Fragile X Syndrome.

Maggie W Guy, John E Richards, Abigail L Hogan, Jane E Roberts

Open access · goldAbstract read
In one paragraph

Article in Frontiers in psychiatry, 2021. 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
0.2field-weighted citation impact, top 49% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

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

4 authors at 2 institutions in 1 country.

Maggie W GuyDepartment of Psychology, Loyola University Chicago, Chicago, IL, United States.
John E RichardsDepartment of Communication Sciences and Disorders, Arnold School of Public Health, University of South Carolina, Columbia, SC, United States.
Abigail L HoganDepartment of Communication Sciences and Disorders, Arnold School of Public Health, University of South Carolina, Columbia, SC, United States.
Jane E RobertsDepartment of Communication Sciences and Disorders, Arnold School of Public Health, University of South Carolina, Columbia, SC, United States.
University of South Carolina · USLoyola University Chicago · US

Funding

Supplement to The Emergence and Stability of Autism in Fragile X SyndromeR01MH090194 · NIMH · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI ROBERTS, JANE E · 2011 to 2020
$5.4M
The Development of Sustained Attention in InfantsR37HD018942 · NICHD · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI RICHARDS, JOHN E · 2007 to 2016
$4.5M
NICHD NIH HHS R37 HD018942NIMH NIH HHS R01 MH090194
6 · The paper itself

Abstract

Fragile X syndrome (FXS) is the leading known genetic cause of autism spectrum disorder (ASD) with 60-74% of males with FXS meeting diagnostic criteria for ASD. Infants with FXS have demonstrated atypical neural responses during face processing that are unique from both typically developing, low-risk infants and infants at high familial risk for ASD (i.e., infants siblings of children with ASD). In the current study, event-related potential (ERP) responses during face processing measured at 12 months of age were examined in relation to ASD symptoms measured at ~48 months of age in participants with FXS, as well as siblings of children with ASD and low-risk control participants. Results revealed that greater amplitude N290 responses in infancy were associated with more severe ASD symptoms in childhood in FXS and in siblings of children with ASD. This pattern of results was not observed for low-risk control participants. Reduced Nc amplitude was associated with more severe ASD symptoms in participants with FXS but was not observed in the other groups. This is the first study to examine ASD symptoms in childhood in relation to infant ERP responses in FXS. Results indicate that infant ERP responses may be predictive of later symptoms of ASD in FXS and the presence of both common and unique pathways to ASD in etiologically-distinct high-risk groups is supported (i.e., syndromic risk vs. familial risk).

Indexed as

autism spectrum disorderchildevent-related potentialsfragile X syndromeinfant

Identifiers

PMID34899412
PMCPMC8651978
OpenAlexW3216986402

What OpenQuestion holds

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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.