Evidence map›Paper›PMID 42293086›Full record

ArticleFrontiers in neurology

Electroencephalographic abnormalities and clinical phenotypes in children with autism spectrum disorder: a single center cohort study.

Natalia Wizner, Michał Wizner, Julia Rokosz, Magdalena Matlakiewicz, Magdalena Hankus, Justyna Paprocka

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Article in Frontiers in neurology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Natalia Wizner *Department of Pediatric Neurology, Faculty of Medical Sciences, Students' Scientific Society, Medical University of Silesia, Katowice, Poland.
Michał Wizner *Department of Pediatric Neurology, Faculty of Medical Sciences, Students' Scientific Society, Medical University of Silesia, Katowice, Poland.
Julia RokoszDepartment of Pediatric Neurology, Faculty of Medical Sciences, Students' Scientific Society, Medical University of Silesia, Katowice, Poland.
Magdalena MatlakiewiczDepartment of Pediatric Neurology, Faculty of Medical Sciences, Students' Scientific Society, Medical University of Silesia, Katowice, Poland.
Magdalena HankusDepartment of Pediatric Neurology, Faculty of Medical Sciences, Medical University of Silesia, Katowice, Poland.
Justyna PaprockaDepartment of Pediatric Neurology, Faculty of Medical Sciences, Medical University of Silesia, Katowice, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Electroencephalographic (EEG) abnormalities are frequently observed in children with autism spectrum disorder (ASD), even in the absence of clinical seizures. However, the clinical significance of different EEG patterns in ASD remains incompletely understood. Objective: To investigate associations between EEG abnormalities and selected clinical characteristics in children with ASD. Methods: This study analyzed medical records of 180 children with ASD hospitalized at the Pediatric Neurology Department at the Upper Silesian Child Health Center in Katowice. Patients were stratified by epilepsy diagnosis and EEG characteristics (normal, non-paroxysmal changes, paroxysmal changes). Clinical variables analyzed included developmental milestones, intellectual disability severity, sleep disturbances, hyperactivity, sensory integration disorders, aggressive behaviors, and motor deficits. Statistical analysis employed Mann-Whitney Results: Sleep disorders showed significant association with EEG pattern type ( Conclusion: Non-paroxysmal EEG abnormalities may represent a distinct neurophysiological correlate of sleep disorders in children with ASD. Comorbid epilepsy is strongly associated with intellectual disability severity, supporting the need for comprehensive neurological evaluation in this population. While broad categorical EEG patterns did not reveal significant associations with most clinical manifestations in our sample, more granular EEG analysis may detect subtle correlations not apparent with our simplified classification approach.

Indexed as

ASDchildrenEEGepilepsyintellectual disabilitysleep disorders

Identifiers

PMID42293086
PMCPMC13259911

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