Pyridoxine‐responsive KCNQ2 epileptic encephalopathy: Additional cases and literature review

Abstract

Abstract Background Typical patients with KCNQ2 (OMIM# 602235) epileptic encephalopathy present early neonatal‐onset intractable seizures with a burst suppression EEG pattern and severe developmental delay or regression, and those patients always fail first‐line treatment with sodium channel blockers. Vitamin B6, either pyridoxine or pyridoxal 50‐phosphate, has been demonstrated to improve seizure control in intractable epilepsy. Methods Here, we collected and summarized the clinical data for four independent cases diagnosed with pyridoxine‐responsive epileptic encephalopathy, and their exome sequencing data. Moreover, we reviewed all published cases and summarized the clinical features, genetic variants, and treatment of pyridoxine‐responsive KCNQ2 epileptic encephalopathy. Results All four cases showed refractory seizures during the neonatal period or infancy, accompanied by global development delay. Four pathogenetic variants of KCNQ2 were uncovered and confirmed by Sanger sequencing: KCNQ2 [NM_172107.4: c.2312C > T (p.Thr771Ile), c.873G > C (p.Arg291Ser), c.652 T > A (p.Trp218Arg) and c.913‐915del (p. Phe305del)]. Sodium channel blockers and other anti‐seizure medications failed to control their seizures. The frequency of seizures gradually decreased after treatment with high‐dose pyridoxine. In case 1, case 2, and case 4, clinical seizures relapsed when pyridoxine was withdrawn, and seizures were controlled again when pyridoxine treatment was resumed. Conclusion Our study suggests that pyridoxine may be a promising adjunctive treatment option for patients with KCNQ2 epileptic encephalopathy.

Keywords

• epileptic encephalopathy
• gene mutation
• KCNQ2
• pyridoxine
• pyridoxine‐responsive