接受生酮饮食的难治性癫痫患者脑内谷胱甘肽增加,癫痫发作负担减轻。

Saman Hazany, Brittany DeClouette, Jessica Lowe, Darryl H Hwang, Paul E Kim, Stefan Bluml, Arthur Partikian
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摘要

背景和目的:生酮饮食(KD)可改善耐药性癫痫患者的癫痫发作控制。由于线粒体谷胱甘肽(GSH)水平的增加可能会导致癫痫发作易感性的改变,我们通过体内 1H 磁共振波谱(1H MRS)量化了大脑中 GSH 绝对水平的变化,并将其与 KD 患者癫痫发作控制程度相关联:最初纳入了五名认知正常的成年耐药性癫痫患者,其中两人完成了研究。神经科医生和注册营养师分别在基线、1 个月、3 个月和 6 个月时对每位患者的癫痫发作状况和开始改良阿特金斯饮食后的饮食依从性进行了评估。在开始生酮饮食之前和6个月时,使用LCModel(6.3-1P版;Stephen Provencher, Oakville, ON, CA)在3特斯拉通用电气磁铁上对顶叶/枕叶灰质和顶叶白质进行短回波时间单象素1H MRS分析,对包括GSH在内的多种代谢物进行量化:两名患者(男性 42 岁,女性 35 岁)的灰质(0.12 至 1.40 和 0.10 至 0.70 国际单位 [IU])和白质(0.65 至 1.50 和 0.80 至 2.00 国际单位)的绝对 GSH 水平都有显著提高,癫痫发作持续时间和频率也改善了 50%。包括酮体在内的其他代谢物未显示出一致的变化:结论:在对两名成年难治性癫痫患者进行的纵向前瞻性研究中观察到,在开始摄入生酮饮食后,患者体内的 GSH 水平明显提高(分别为 7 倍和 14 倍),癫痫发作改善了 50%。这项试验研究支持 GSH 在大脑中可能发挥的抗惊厥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Brain Glutathione Increase and Seizure Burden Decrease in Patients with Intractable Epilepsy on Ketogenic Diet.

Background and purpose: Ketogenic diet (KD) improves seizure control in patients with drug-resistant epilepsy. As increased mitochondrial levels of glutathione (GSH) might contribute to a change in seizure susceptibility, we quantified changes of absolute GSH levels in the brain by in vivo 1H magnetic resonance spectroscopy (1H MRS) and correlate that with degree of seizure control in patients on KD.

Methods: Five cognitively normal adult patients with drug-resistant epilepsy were initially included and 2 completed the study. Each patient was evaluated by a neurologist and registered dietitian at baseline, 1, 3, and 6 months for seizure status and diet adherence after initiation of a modified atkins diet. Multiple metabolites including GSH were quantified using LCModel (version 6.3-1P; Stephen Provencher, Oakville, ON, CA) on a short echo time single-voxel 1H MRS in parieto/occipital grey matter and parietal white matter on a 3 Tesla General Electric magnet prior to starting the ketogenic diet and at 6 months.

Results: Both patients (42-years-old male and 35-years-old female) demonstrated marked increases in absolute GSH level in both gray matter (0.12 to 1.40 and 0.10 to 0.70 international unit [IU]) and white matter (0.65 to 1.50 and 0.80 to 2.00 IU), as well as 50% improvements in seizure duration and frequency. Other metabolites including ketone bodies did not demonstrate consistent changes.

Conclusions: Markedly increased levels of GSH (7-fold and 14-fold) were observed in longitudinal prospective study of two adult patients with intractable epilepsy with 50% seizure improvement after initiation of ketogenic diets. This pilot study supports the possible anticonvulsant role of GSH in the brain.

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