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Cognitive development in children with new onset epilepsy
Paul J Rathouz1, Qianqian Zhao, Jana E Jones
1Department of Biostatistics & Medical Informatics, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA.
Insights
Cognitive deficits in children with epilepsy are present at diagnosis and remain stable, not worsening over time. Early intervention is crucial for these children who show developmental lags compared to peers.
Area of Science:
- Pediatric Neurology
- Neurodevelopmental Disorders
- Epilepsy Research
Background:
- Epilepsy is a common neurological disorder in children.
- Cognitive development in pediatric epilepsy is a significant concern.
- Longitudinal data on cognitive trajectories in pediatric epilepsy are limited.
Purpose of the Study:
- To track cognitive development in children with new or recent onset epilepsy.
- To compare cognitive trajectories between epilepsy subtypes and typical development.
- To determine if cognitive deficits in pediatric epilepsy worsen, improve, or remain stable over 5-6 years.
Main Methods:
- Neuropsychological assessments were conducted on 69 children with epilepsy (aged 8-18) at diagnosis, 2 years, and 5-6 years post-diagnosis.
- A comparison group of 62 typically developing children was assessed at each time point.
- Cognitive domains evaluated included intelligence, academic achievement, language, executive function, and psychomotor speed.
- Data were analyzed using mixed-effects regression models, stratified by epilepsy syndrome (localization-related epilepsy [LRE] and idiopathic generalized epilepsy [IGE]).
Main Results:
- Cognitive abnormalities in arithmetic, response inhibition, attention, fine motor dexterity, and psychomotor speed were evident at diagnosis (p < 0.001).
- These deficits remained largely stable over the 5-6 year follow-up period, with no significant worsening or recovery.
- Children with LRE generally performed better than those with IGE on specific measures (arithmetic, response inhibition, psychomotor speed).
Conclusions:
- Cognitive development in children with LRE and IGE does not show progressive decline but rather a persistent lag compared to typically developing children.
- Identified cognitive abnormalities are present early and persist over time.
- Early detection and intervention are essential for managing cognitive deficits in pediatric epilepsy.
Aim:
To characterize the prospective trajectory of cognitive development in children with new or recent onset epilepsy from baseline to 5 to 6 years after diagnosis.
Method:
Sixty-nine children (40 males, 29 females; age 8-18y), with new or recent onset epilepsies underwent neuropsychological assessment shortly after diagnosis (Wave 1), 2 years (Wave 2), and 5 to 6 years after diagnosis (Wave 3). Intelligence, academic achievement, language, executive function, and psychomotor speed were evaluated. Sixty-two children (28 males, 34 females; age 8-18) with typical development served as a comparison group at each time point. The cognitive data were examined by syndrome (localization-related epilepsy [LRE]; idiopathic generalized epilepsy [IGE]; comparison group). Mixed effect regression models compared trajectories among groups with respect to time since diagnosis.
Results:
Cognitive abnormalities exhibited by children with epilepsy in arithmetic computation, response inhibition, attention, fine motor dexterity, and psychomotor speed (all p values <0.001), are detectable at or near the time of diagnosis and largely remain stable over the ensuing 5 to 6 years without evidence of progressive worsening or recovery. This course is evident across both LRE and IGE groups, with the LRE group performing better for some outcomes (arithmetic, response inhibition, psychomotor speed) and never worse than the IGE group.
Interpretation:
Cognitive development in children with LRE and IGE is not characterized by progressive deterioration or lack of age-appropriate development; rather, development lags behind that of children with typical development. Cognitive abnormalities, when detected, are present near the time of diagnosis, persist over time, and require early intervention.
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