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从改良阿特金斯饮食切换到传统生酮饮食是否会改善癫痫发作控制?

Will seizure control improve by switching from the modified Atkins diet to the traditional ketogenic diet?

机构信息

Neurology, The Johns Hopkins University, Baltimore, Maryland, USA.

出版信息

Epilepsia. 2010 Dec;51(12):2496-9. doi: 10.1111/j.1528-1167.2010.02774.x. Epub 2010 Nov 10.

Abstract

It has been reported that children can maintain seizure control when the ketogenic diet (KD) is transitioned to the less-restrictive modified Atkins diet (MAD). What is unknown, however, is the likelihood of additional seizure control from a switch from the MAD to the KD. Retrospective information was obtained from 27 patients who made this dietary change from four different institutions. Ten (37%) patients had ≥10% additional seizure reduction with the KD over the MAD, of which five became seizure-free. The five children who did not improve on the MAD failed to improve when transitioned to the KD. A higher incidence of improvement with the KD occurred for those with myoclonic-astatic epilepsy (70% vs. 12% for all other etiologies, p = 0.004), including all who became seizure-free. These results suggest that the KD probably represents a "higher dose" of dietary therapy than the MAD, which may particularly benefit those with myoclonic-astatic epilepsy.

摘要

据报道,当酮饮食(KD)转换为限制较少的改良阿特金斯饮食(MAD)时,儿童可以维持癫痫发作控制。然而,尚不清楚从 MAD 转换为 KD 是否会有更多的癫痫发作控制。从四个不同机构的 27 名患者那里获得了回顾性信息,这些患者进行了这种饮食改变。在 KD 中,有 10 名(37%)患者的癫痫发作减少了≥10%,其中 5 名患者癫痫发作停止。在 MAD 上没有改善的 5 名儿童在转换为 KD 时也没有改善。KD 改善的发生率更高,见于肌阵挛-站立性癫痫(70%,而所有其他病因的为 12%,p=0.004),包括所有癫痫发作停止的患者。这些结果表明,KD 可能代表比 MAD 更高剂量的饮食治疗,这可能特别有益于肌阵挛-站立性癫痫患者。

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