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Response to anti-seizure medications in children carrying novel or previously reported HCN1 gene variants
Marium N Khan1, Nicholas P Poolos1
1Department of Neurology and Regional Epilepsy Center, University of Washington, Seattle, WA, USA.
Insights
Mutations in the HCN1 gene cause a rare epilepsy syndrome. Valproate and clobazam improved seizures in affected children, while lamotrigine and oxcarbazepine worsened them, indicating specific anti-seizure medication (ASM) efficacy trends.
Area of Science:
- Genetics and Neurology
- Epilepsy Research
- Ion Channel Function
Background:
- HCN1 gene variants are associated with childhood epilepsy and developmental disability, often presenting as early infantile epileptic encephalopathy (EIEE).
- Seizures in this syndrome can be drug-resistant, with some anti-seizure medications (ASMs) potentially exacerbating symptoms.
Purpose of the Study:
- To investigate the efficacy of various ASMs in children with HCN1-related epilepsy.
- To identify novel HCN1 variants and characterize their phenotypic associations.
Main Methods:
- A registry of 10 children with HCN1 variants and refractory epilepsy was compiled through online parent groups and direct outreach.
- Parents completed detailed surveys on genetic testing, developmental status, and responses to ASMs, with medical records providing documentation.
Main Results:
- Five novel HCN1 variants were identified, with some mapping to the ion channel transmembrane domain correlating with more severe phenotypes.
- Valproate and clobazam improved seizure frequency in affected children, with two achieving seizure freedom.
- Lamotrigine and oxcarbazepine were associated with exacerbated seizure frequency.
Conclusions:
- This study identifies novel HCN1 variants and provides crucial data on ASM efficacy in HCN1-related epilepsy.
- The observed trends in ASM efficacy parallel those in Dravet syndrome, suggesting potential shared pathogenic mechanisms in EIEE.
- Valproate and clobazam show promise as effective treatments, while lamotrigine and oxcarbazepine should be used with caution.
Objective:
Variants in the HCN1 gene cause a syndrome of childhood epilepsy and developmental disability with a broad phenotypic range. Many affected children manifest with early infantile epileptic encephalopathy (EIEE) and highly drug-resistant epilepsy. There are anecdotal reports that seizures in this syndrome are exacerbated by some anti-seizure medications (ASMs), including lamotrigine and lacosamide. However, the efficacy of most ASMs in this disorder is unknown. We sought to understand which ASMs were most effective.
Methods:
We compiled a registry of 10 children with HCN1 variants and refractory epilepsy via outreach to parent members of an online social affinity group, and from unsolicited parent outreach to us. Parents filled out an eight-page survey detailing their child's and parents' genetic testing results, child's developmental status, and response to ASMs. Outside medical records were provided that documented genetic testing results.
Results:
Five of these variants had not been previously reported in the literature. Of these, there was phenotypic variability depending on where the variant mapped on the HCN1 ion channel structure, with variants mapping to an ion channel transmembrane domain causing more severe phenotypes. Subjects given lamotrigine or oxcarbazepine had exacerbated seizure frequency whereas those exposed to valproate or clobazam had improved seizure frequency, with two subjects becoming seizure-free.
Significance:
We report here five novel HCN1 variants. We also provide a novel survey of ASM efficacy. These trends in ASM efficacy are similar to what has been observed in Dravet syndrome, another EIEE, raising questions about potential common pathogenic mechanisms at a cellular level.
Plain Language Summary:
We surveyed families whose children had been diagnosed with a rare epilepsy syndrome due to mutations in the HCN1 gene. In reviewing their genetic testing results, we discovered five new gene mutations (variants) that had not been previously reported. We also asked which anti-seizure medications had been most effective: they cited valproate and clobazam as most effective, while lamotrigine and oxcarbazepine made seizures worse.
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