Evidence map›Paper›PMID 42116138›Full record

ArticleBMC psychology2026

Heterogeneous neurocognitive signatures in early childhood autism: a combined analysis of pharmacological treatment and gender.

Öznur Özge Özcan, Burcu Çevreli, Mehmet Kamali, Türker Tekin Ergüzel

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Article in BMC psychology, 2026. 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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Öznur Özge ÖzcanMolecular Biology and Genetics, Faculty of Engineering and Natural Sciences, Üsküdar University, Altunizade Neighborhood, University Street No: 14, Üsküdar, Istanbul, 34662, Turkey. oznurozge.ozcan@uskudar.edu.tr.ORCID http://orcid.org/0000-0001-8992-0556
Burcu ÇevreliDepartment of Physiology, Faculty of Medicine, Üsküdar University, İstanbul, Turkey.
Mehmet KamaliNeuroscience, Health Sciences Institute, Üsküdar University, Istanbul, Turkey.
Türker Tekin ErgüzelDepartment of Software Engineering, Faculty of Engineering and Natural Sciences, Üsküdar University, Istanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAutism spectrum disorder (ASD) is characterized by marked heterogeneity in sensory processing, self-regulation, and executive functioning during early childhood. Pharmacological treatments are widely used to manage behavioral symptoms; however, their role in shaping multidomain neurocognitive profiles remains unclear. This study aimed to determine whether neurocognitive profiles differ as a function of pharmacological treatment type (antipsychotic, ADHD medication, or no medication) and gender children with ASD in early childhood.

methodsThis cross-sectional study included 350 children aged 4-6 years diagnosed with ASD. Participants were stratified into three groups based on current pharmacological treatment: antipsychotic-treated (n = 115), ADHD-medicated (n = 110), and medication-free (n = 125), with balanced gender distribution. Parents completed the Parent-Rated Sensory Reactivity Scale (ESRS), the Self-Regulation Skills Scale-Parent Form (SRSS-P), and the Childhood Executive Functioning Inventory-Parent Form (CEFI-P). Autism severity was assessed using the Childhood Autism Rating Scale (CARS). Group differences were examined using ANOVA, followed by correlation and multiple regression analyses.

resultsNeurocognitive profiles differed significantly across pharmacological treatment groups (p < 0.01). Children receiving antipsychotic medication exhibited higher sensory reactivity and greater autism severity, whereas those receiving ADHD medication showed greater impairments in executive functioning and self-regulation. Medication-free children consistently demonstrated the lowest levels of impairment. Gender showed a limited moderating effect, with some domain-specific differences observed across treatment groups. Correlation and regression analyses indicated that pharmacological treatment and gender were associated with variability in neurocognitive domains and overall autism severity (R² = 0.46).

conclusionsPharmacological treatment type and gender are important factors associated with heterogeneity in neurocognitive profiles in early childhood (4-6 years) ASD. These findings suggest that medication-related differences extend beyond behavioral symptom control and are linked to distinct sensory, regulatory, and executive functioning patterns. Clinically, this highlights the importance of considering treatment type and gender when interpreting neurodevelopmental profiles and when planning individualized, multidomain interventions.

Indexed as

Antipsychotic AgentsAutism Spectrum DisorderExecutive FunctionAttention Deficit Disorder with HyperactivityChildChild, PreschoolCross-Sectional StudiesFemaleHumansMaleSelf-ControlSeverity of Illness IndexSex FactorsAntipsychotic Agentsautism spectrum disorderearly childhoodexecutive functioninggenderindividual differencespharmacological interventionsself-regulationsensory processing

Identifiers

PMID42116138
PMCPMC13330274

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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.