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K.Vita:一种中链甘油三酯混合物用于治疗耐药性癫痫的可行性研究。

K.Vita: a feasibility study of a blend of medium chain triglycerides to manage drug-resistant epilepsy.

作者信息

Schoeler Natasha E, Orford Michael, Vivekananda Umesh, Simpson Zoe, Van de Bor Baheerathi, Smith Hannah, Balestrini Simona, Rutherford Tricia, Brennan Erika, McKenna James, Lambert Bridget, Barker Tom, Jackson Richard, Williams Robin S B, Sisodiya Sanjay M, Eaton Simon, Heales Simon J R, Cross J Helen, Walker Matthew C

机构信息

UCL Great Ormond Street Institute of Child Health, London, UK.

Great Ormond Street Hospital for Children, London, UK.

出版信息

Brain Commun. 2021 Jul 23;3(4):fcab160. doi: 10.1093/braincomms/fcab160. eCollection 2021.

Abstract

This prospective open-label feasibility study aimed to evaluate acceptability, tolerability and compliance with dietary intervention with K.Vita, a medical food containing a unique ratio of decanoic acid to octanoic acid, in individuals with drug-resistant epilepsy. Adults and children aged 3-18 years with drug-resistant epilepsy took K.Vita daily whilst limiting high-refined sugar food and beverages. K.Vita was introduced incrementally with the aim of achieving ≤35% energy requirements for children or 240 ml for adults. Primary outcome measures were assessed by study completion, participant diary, acceptability questionnaire and K.Vita intake. Reduction in seizures or paroxysmal events was a secondary outcome. 23/35 (66%) children and 18/26 (69%) adults completed the study; completion rates were higher when K.Vita was introduced more gradually. Gastrointestinal disturbances were the primary reason for discontinuation, but symptoms were similar to those reported from ketogenic diets and incidence decreased over time. At least three-quarters of participants/caregivers reported favourably on sensory attributes of K.Vita, such as taste, texture and appearance, and ease of use. Adults achieved a median intake of 240 ml K.Vita, and children 120 ml (19% daily energy). Three children and one adult had ß-hydroxybutyrate >1 mmol/l. There was 50% (95% CI 39-61%) reduction in mean frequency of seizures/events. Reduction in seizures or paroxysmal events correlated significantly with blood concentrations of medium chain fatty acids (C10 and C8) but not ß-hydroxybutyrate. K.Vita was well accepted and tolerated. Side effects were mild and resolved with dietetic support. Individuals who completed the study complied with K.Vita and additional dietary modifications. Dietary intervention had a beneficial effect on frequency of seizures or paroxysmal events, despite absent or very low levels of ketosis. We suggest that K.Vita may be valuable to those with drug-resistant epilepsy, particularly those who cannot tolerate or do not have access to ketogenic diets, and may allow for more liberal dietary intake compared to ketogenic diets, with mechanisms of action perhaps unrelated to ketosis. Further studies of effectiveness of K.Vita are warranted.

摘要

这项前瞻性开放标签可行性研究旨在评估一种名为K.Vita的医用食品(其癸酸与辛酸比例独特)对耐药性癫痫患者进行饮食干预的可接受性、耐受性和依从性。3至18岁的耐药性癫痫成人和儿童每天服用K.Vita,同时限制高糖精制食品和饮料。K.Vita逐步引入,目标是满足儿童≤35%的能量需求或成人240毫升的摄入量。主要结局指标通过研究完成情况、参与者日记、可接受性问卷和K.Vita摄入量进行评估。癫痫发作或阵发性事件的减少是次要结局。23/35(66%)的儿童和18/26(69%)的成人完成了研究;K.Vita引入得越缓慢,完成率越高。胃肠道不适是停药的主要原因,但症状与生酮饮食报告的症状相似,且发生率随时间下降。至少四分之三的参与者/照顾者对K.Vita的感官属性(如味道、质地和外观)以及易用性给予了好评。成人K.Vita的摄入量中位数为240毫升,儿童为120毫升(占每日能量的19%)。三名儿童和一名成人的β-羟基丁酸>1毫摩尔/升。癫痫发作/事件的平均频率降低了50%(95%置信区间39 - 61%)。癫痫发作或阵发性事件的减少与中链脂肪酸(C10和C8)的血药浓度显著相关,但与β-羟基丁酸无关。K.Vita被很好地接受和耐受。副作用轻微,通过饮食支持得以缓解。完成研究的个体遵守了K.Vita及其他饮食调整。尽管酮症水平缺乏或极低,但饮食干预对癫痫发作或阵发性事件的频率有有益影响。我们认为,K.Vita可能对耐药性癫痫患者有价值,特别是那些不能耐受或无法采用生酮饮食的患者,并且与生酮饮食相比,可能允许更自由的饮食摄入,其作用机制可能与酮症无关。有必要对K.Vita的有效性进行进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8294/8557697/8ce5897428a9/fcab160f5.jpg

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