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Updated: Apr 6, 2026

A Behavioral Screen for Heat-Induced Seizures in Mouse Models of Epilepsy
Published on: July 12, 2021
No association between ApoE polymorphism and febrile seizures
Pierre Lavenex1,2, Pamela Banta Lavenex3, François Cachat4
1Laboratory for Experimental Research on Behavior, Institute of Psychology, University of Lausanne, 1015, Lausanne, Switzerland. pierre.lavenex@unil.ch.
Insights
Simple febrile seizures in children are not linked to specific apolipoprotein E (ApoE) gene variants. This study found no association between ApoE alleles and the occurrence of simple febrile seizures in early childhood.
Area of Science:
- Genetics
- Pediatrics
- Neurology
Background:
- Febrile seizures affect 2-7% of children aged 3 months to 5 years.
- Differentiating febrile seizures from other seizure types is crucial for appropriate care.
- The apolipoprotein E (ApoE) gene's role in neurological conditions is under investigation.
Purpose of the Study:
- To investigate the hypothesis that the ApoE2 allele is preferentially carried by children with simple febrile seizures who do not develop epilepsy later.
- To determine if ApoE gene polymorphism is associated with simple febrile seizures.
Main Methods:
- Genotyping of ApoE alleles in children with simple febrile seizures (n=93) and typically developing controls (n=80).
- Analysis of allele and genotype frequencies.
- Assessment for Hardy-Weinberg equilibrium.
Main Results:
- No significant differences in ApoE allele or genotype distribution were found between the simple febrile seizure group and the control group.
- Observed allele frequencies were ApoE2 (0.064), ApoE3 (0.829), and ApoE4 (0.107).
- Frequencies were consistent with Hardy-Weinberg equilibrium, indicating population stability.
Conclusions:
- The study did not find an association between ApoE gene alleles and the occurrence of simple febrile seizures.
- ApoE polymorphism does not appear to be a risk factor for simple febrile seizures in the studied population.
Abstract:
Seizures associated with fever are a common pediatric problem, affecting about 2-7 % of children between 3 months and 5 years of age. Differentiation of febrile seizures from acute symptomatic seizures secondary to central nervous system infections or seizures associated with fever in children with epilepsy is essential to provide appropriate treatment and follow-up care. Here, we tested the hypothesis that children who exhibit simple febrile seizures during early childhood, but do not develop epileptic seizures later in life, might preferentially carry the ApoE2 allele of the gene coding for the apolipoprotein E. We did not find any differences in the distribution of ApoE alleles or genotypes between individuals who exhibited simple febrile seizures (n = 93) and age-matched, typically developing subjects (n = 80). We found that the observed allele and genotype frequencies did not deviate from Hardy-Weinberg equilibrium, which suggests that the frequencies of ApoE alleles and genotypes are stable in the Swiss population from which our samples were derived. Across both groups of subjects (n = 173), we found an ApoE2 allele frequency of 0.064, an ApoE3 frequency of 0.829 and an ApoE4 frequency of 0.107. Our findings are consistent with previous reports of the distribution of ApoE polymorphism for European subjects free of any neurological disorders, and show that the different alleles of the gene coding for the apolipoprotein E are not associated with the occurrence of simple febrile seizures.
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