Evidence map›Paper›PMID 42282790›Full record

ArticlebioRxiv : the preprint server for biology2026

Asymmetric neural dynamics of visuospatial attention in autism spectrum disorder.

Megan Darrell, Theo Vanneau, Chloe Brittenham, John J Foxe, Sophie Molholm

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

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.

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

5 authors.

Megan DarrellMedical Scientist Training Program, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0001-6498-9442
Theo VanneauThe Cognitive Neurophysiology Laboratory, Department of Pediatrics, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0002-5750-7051
Chloe BrittenhamThe Cognitive Neurophysiology Laboratory, Department of Pediatrics, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0002-1867-2660
John J FoxeDominic P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0002-4300-3098
Sophie MolholmDominic P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0003-1870-7306

Funding

University of Rochester Intellectual and Developmental Disabilities Research CenterP50HD103536 · NICHD · UNIVERSITY OF ROCHESTER · PI JOHN J FOXE, Anna K Majewska · 2020 to 2026
$9.8M
Medical Scientist Training ProgramT32GM149364 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI Myles H. Akabas · 2023 to 2026
$7.5M
SUPPORT FOR THE ROSE F KENNEDY IDDRC P50P50HD105352 · NICHD · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SOPHIE MOLHOLM, Steven Upshaw Walkley · 2021 to 2026
$7.0M
NICHD NIH HHS P50 HD103536NICHD NIH HHS P50 HD105352NIGMS NIH HHS T32 GM149364
6 · The paper itself

Abstract

Background: Selective attention enables the prioritization of behaviorally relevant information in complex sensory environments. Despite substantial evidence for altered attention in autism spectrum disorder (ASD), the neurophysiological mechanisms underlying these differences remain poorly understood. Methods: Here, we integrate high-density electroencephalography (EEG), pupillometry, and behavioral measures collected during a cued covert visuospatial selective attention task to characterize mechanisms of spatial attention in children and adolescents with ASD (n = 18; 13.4 ± 3.0 YO), and how they differ from age- and IQ- matched individuals with typical-development (TD) (n = 21; 14.7 ± 3.8 YO). Results: Both groups demonstrated high target detection accuracy and comparable response times, with no significant between-group differences in behavioral performance. Furthermore, neurophysiological measures demonstrated that during leftward attention, both TD and ASD participants exhibited canonical attentional processes, including lateralized anticipatory parieto-occipital alpha modulation and enhanced P1 sensory responses to attended stimuli. Additionally, across both groups, trial-level analyses revealed that decreased anticipatory alpha power and increased P1 amplitude contralateral to the attended hemifield were associated with faster reaction times. In contrast, there were notable group differences in the neural dynamics supporting rightward spatial attention. TD participants showed early sensory gain (P1 modulation) without alpha-band modulation, whereas ASD participants exhibited modulation of posterior alpha power without effective sensory gain. Interestingly, for rightward attention, only P1 amplitude predicted reaction time, and this was the case for both groups. Resting-state alpha dynamics did not differ between groups, indicating that the attended hemifield differences reflect task-dependent differences in attentional control rather than baseline oscillatory differences. Limitations: Limitations include modest sample size and restriction to autistic individuals with relatively low support needs, which may limit the generalizability of these findings to the broader autism spectrum. Conclusions: The similarity of leftward attention mechanisms across groups, which includes intact recruitment of anticipatory alpha modulation, argues against a global disruption of basic visuo-spatial attentional function in autistic individuals with low support needs. However, group differences emerged specifically during rightward attention, where ASD participants showed a more uniform pattern of oscillatory modulation, warranting further investigation. Collectively, these findings provide novel insight into the neural architecture of visuospatial attention in ASD, revealing how preparatory oscillatory activity shapes early sensory responses and behavior during selective attention.

Indexed as

autism spectrum disorderEEGpseudoneglectvisuospatial attention

Identifiers

PMID42282790
PMCPMC13251917

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.