# Oxcarbazepine may be an effective option for Chinese pediatric patients with self-limited focal epilepsy of neonatal/infantile onset: a retrospective cohort study

**Authors:** Na Sun, Xueying Wang, Shaoping Huang, Lin Yang, Dan Li

PMC · DOI: 10.3389/fped.2025.1509660 · Frontiers in Pediatrics · 2025-04-01

## TL;DR

This study found that oxcarbazepine can be an effective treatment for Chinese children with a specific type of early-onset epilepsy when initial medications fail.

## Contribution

The study identifies oxcarbazepine as a potentially effective second-line treatment for SeLFE in Chinese pediatric patients.

## Key findings

- Half of the children achieved complete seizure control with first-line monotherapy.
- Nine out of twelve children who failed initial treatment became seizure-free with oxcarbazepine.
- No pathogenic genetic abnormalities were found in 16 children, while PRRT2, SCN2A, and KCNQ2 were identified in others.

## Abstract

The aim of this study was to evaluate the long-term follow-up data of Chinese children with self-limited focal epilepsy with neonatal/infantile onset (SeLFE) and to investigate the clinical features, genetic background and treatment outcomes of this type of epileptic syndrome.

We conducted a retrospective cohort study of twenty-six children with SeLFE admitted to or followed by the Department of Pediatrics, Second Affiliated Hospital of Xi'an Jiaotong University from October 2011 to October 2021. Treatment decisions were based on the children's seizure semiology, frequency, economy, medication accessibility, allergies and other factors, and initial medications including levetiracetam, phenobarbital and oxcarbazepine. All children were followed up regularly in the outpatient clinic.

The 26 children, 13 male and 13 female, were followed for a mean of 54.0 (49.0, 58.5) months. Trio whole-exome sequencing (WES) revealed no pathogenic genetic abnormalities in 16 children, and known pathological genes including PRRT2, SCN2A and KCNQ2 were detected in 10 children. Thirteen children (50.0%) achieved complete seizure control after first-line monotherapy. Among the 12 patients who failed to respond to the first monotherapy, 9 patients achieved a seizure free status with oxcarbazepine, which was used as the second-line monotherapy or as add-on therapy. One patient recovered spontaneously without treatment.

Although SeLFE is often self-limited, this study showed that complete seizure control is not always achieved with initial medication therapy. Oxcarbazepine may be an effective option for the treatment of SeLFE.

## Linked entities

- **Genes:** PRRT2 (proline rich transmembrane protein 2) [NCBI Gene 112476], SCN2A (sodium voltage-gated channel alpha subunit 2) [NCBI Gene 6326], KCNQ2 (potassium voltage-gated channel subfamily Q member 2) [NCBI Gene 3785]
- **Chemicals:** oxcarbazepine (PubChem CID 34312), levetiracetam (PubChem CID 5284583), phenobarbital (PubChem CID 4763)

## Full-text entities

- **Genes:** KCNQ2 (potassium voltage-gated channel subfamily Q member 2) [NCBI Gene 3785] {aka BFNC, DEE7, EBN, EBN1, ENB1, HNSPC}, SCN2A (sodium voltage-gated channel alpha subunit 2) [NCBI Gene 6326] {aka BFIC3, BFIS3, BFNIS, DEE11, EA9, EIEE11}, PRRT2 (proline rich transmembrane protein 2) [NCBI Gene 112476] {aka BFIC2, BFIS2, DSPB3, DYT10, EKD1, FICCA}
- **Diseases:** seizure (MESH:D012640), genetic abnormalities (MESH:D030342), epileptic syndrome (MESH:D000073376), focal epilepsy (MESH:D004828), allergies (MESH:D004342)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC11998760/full.md

## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC11998760/full.md

---
Source: https://tomesphere.com/paper/PMC11998760