Abstract

AimTo evaluate the efficacy of anti-seizure medications (ASMs), quinidine, and ketogenic diet therapy (KDT) for KCNT1-related epilepsy and to explore genotype-efficacy correlations.MethodsWe collected the data for KCNT1-related epilepsy cases from our hospital's medical records and the literature. In total, 50 patients received quinidine, 23 received classical KDT, and 15 received ASMs; all ASM data were from our hospital owing to the lack of detailed ASM data in the literature. The efficacy rates (ERs) of the treatments were compared; an ER that reduced the number of seizures by ≥50% was considered positive. Efficacy according to genotype was also assessed.ResultsThe ERs for the 30 patients at our hospital were 40, 26.7, 30, and 44.4% for all treatments, ASMs, quinidine, and KDT, respectively. For all patients (ours and those in previous reports), the overall ERs for quinidine and KDT were 26.0 and 43.5%, respectively (P = 0.135). The ERs for quinidine and KDT in functional domain variant-related epilepsy differed significantly (20.6 vs. 53.8%; P = 0.037).InterpretationKDT may be better at treating KCNT1-related epilepsy than quinidine; ASMs were the least effective. KDT is a viable treatment option for functional domain variant-related epilepsy.

Highlights

  • KCNT1 encodes a Na+-activated K+ channel named Slo2.2, Slack, or KCa4.1

  • Interpretation: ketogenic diet therapy (KDT) may be better at treating KCNT1-related epilepsy than quinidine; anti-seizure medication (ASM) were the least effective

  • Data were collected from 30 patients treated for KCNT1-related epilepsy at our hospital [17 boys and 13 girls; age at onset, 1.25 (0.04–36) months]

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Summary

Introduction

Slo2.2 is the largest known K+ channel and is mainly distributed in the frontal cortex of the brain [1]. It consists of six transmembrane segments (S1–S6), with a pore domain between S5 and S6 and a cytoplasmic C-terminal domain [2, 3]. C>A, pAla259Asp c.808C>G, p.Gln270Glu. 1/1 0 0 1/1 1/5 0 2/3 0 0 regulators of K+ conductance (RCKs) and a nicotinamide adenine dinucleotide-binding domain. 1/1 0 0 1/1 1/5 0 2/3 0 0 regulators of K+ conductance (RCKs) and a nicotinamide adenine dinucleotide-binding domain These subunits exist in the form of tetramers and mediate the channel’s allosteric regulation by ligands [2, 3]

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