# Genetic susceptibility for neurodevelopmental disorders in children born to women with epilepsy

**Authors:** Mathilde Kinge-Rasmussen, Emilie Willoch Olstad, Marte-Helene Bjørk, Hedvig Marie Egeland Nordeng, Manuela M X Tan, Kristina Gervin, Kaja Kristine Selmer

PMC · DOI: 10.1093/braincomms/fcag078 · Brain Communications · 2026-03-16

## TL;DR

Children of mothers with epilepsy may have higher genetic risk for ADHD-related traits, but not for ASD, compared to the general population.

## Contribution

The study evaluates genetic susceptibility for ADHD and ASD in children of mothers with epilepsy using polygenic risk scores.

## Key findings

- Children of mothers with epilepsy had higher ADHD polygenic risk scores compared to the general population.
- ADHD polygenic risk scores were more strongly associated with hyperactivity and inattention in these children.
- ASD polygenic risk scores showed stronger associations with motor and language difficulties in children of mothers with epilepsy.

## Abstract

Children of women with epilepsy have higher rates of neurodevelopmental disorders including attention-deficit/hyperactivity disorder (ADHD) and autism spectrum disorder (ASD), than the general population. This likely reflects a complex gene-environment interplay, but the specific contribution of genetic susceptibility, independent of in utero antiseizure medication exposure, remains unclear. The objective of this study was to evaluate whether polygenic risk scores (PRSs) for ADHD and ASD are elevated in these children compared to the general population and to assess associations with childhood neurodevelopmental traits. We analysed genetic and questionnaire data from the Norwegian Mother, Father and Child Cohort Study (MoBa). We included children born to women with epilepsy (n = 422) and children of mothers without epilepsy (n = 73 300). The parent-reported neurodevelopmental traits hyperactivity, inattention, social difficulties, language difficulties, repetitive behaviour and motor difficulties were measured using z scores at ages 0.5, 1.5, 3, 5 and 8 years. The genetic susceptibility was calculated as PRSs for ADHD and ASD. Children born to women with epilepsy had higher PRSs for ADHD (mean difference = 0.09, P = 0.07), not ASD (mean difference = 0.014, P = 0.78), compared to those without epilepsy. In these children, we observed stronger associations between the ADHD PRSs and neurodevelopmental traits closely linked to ADHD, specifically hyperactivity and inattention for all ages examined with the strongest association at 8 years. For the ASD PRSs, we observed stronger associations with motor development and language difficulties particularly at 5 years in children born to women with epilepsy. Although these associations were in the same direction and statistically significant for all ages in the general population, they did not reach statistical significance in children born to women with epilepsy. Findings from this study show that the ADHD and ASD PRSs were more strongly associated with hyperactivity/inattention, and with language/motor difficulties respectively in children born to women with epilepsy, compared to the general population. However, statistical significance was not reached likely due to limited sample size. These findings underscore the importance of considering genetic predisposition when assessing neurodevelopmental risks in this population.

Kinge-Rasmussen et al. found that associations between polygenic risk scores for attention-deficit/hyperactivity disorder and autism spectrum disorder and corresponding neurodevelopmental traits were stronger—but not statistically significant—among children of mothers with epilepsy compared with those in the general population.

Graphical AbstractFor image description, please refer to the figure legend and surrounding text.

## Linked entities

- **Diseases:** epilepsy (MONDO:0005027), attention-deficit/hyperactivity disorder (MONDO:0007743), autism spectrum disorder (MONDO:0005258)

## Full-text entities

- **Diseases:** hyperactivity (MESH:D006948), inattention (MESH:D001308), neurodevelopmental disorders (MESH:D002658), epilepsy (MESH:D004827), motor difficulties (MESH:D051346), ADHD (MESH:D001289), language difficulties (MESH:D007806), ASD (MESH:D000067877), repetitive behaviour (MESH:D012090)
- **Chemicals:** antiseizure (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC13022828/full.md

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Source: https://tomesphere.com/paper/PMC13022828