奎尼丁
癫痫
医学
发作性
病历
不利影响
生酮饮食
麻醉
内科学
药理学
精神科
作者
Zehong Lin,Tian Sang,Ying Yang,Yuan Wu,Yan Dong,Taoyun Ji,Yuehua Zhang,Ye Wu,Kai Gao,Yuwu Jiang
标识
DOI:10.3389/fneur.2021.834971
摘要
Aim To evaluate the efficacy of anti-seizure medications (ASMs), quinidine, and ketogenic diet therapy (KDT) for KCNT1 -related epilepsy and to explore genotype-efficacy correlations. Methods We 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. Results The 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). Interpretation KDT 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.
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