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Lysine-Restricted Diet as Adjunct Therapy for Pyridoxine-Dependent Epilepsy: The PDE Consortium Consensus Recommendations

机译:赖氨酸限制饮食作为吡P醇依赖性癫痫的辅助疗法:PDE联盟共识建议

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摘要

Background: Seventy-five percent of patients with pyridoxine-dependent epilepsy (PDE) due to Antiquitin (ATQ) deficiency suffer from developmental delay and/or intellectual disability (IQ < 70) despite seizure control. An observational study showed that adjunct treatment with a lysine-restricted diet is safe, results in partial normalization of lysine intermediates in body fluids, and may have beneficial effects on seizure control and psychomotor development.Methods: In analogy to the NICE guideline process, the international PDE Consortium, an open platform uniting scientists and clinicians working in the field of this metabolic epilepsy, during four workshops (2010–2013) developed a recommendation for a lysine-restricted diet in PDE, with the aim of standardizing its implementation and monitoring of patients. Additionally, a proposal for a further observational study is suggested.Results: (1) All patients with confirmed ATQ deficiency are eligible for adjunct treatment with lysine-restricted diet, unless treatment with pyridoxine alone has resulted in complete symptom resolution, including normal behavior and development. (2) Lysine restriction should be started as early as possible; the optimal duration remains undetermined. (3) The diet should be implemented and the patient be monitored according to these recommendations in order to assure best possible quality of care and safety.Discussion: The implementation of this recommendation will provide a unique and a much needed opportunity to gather data with which to refine the recommendation as well as improve our understanding of outcomes of individuals affected by this rare disease. We therefore propose an international observational study that would utilize freely accessible, online data sharing technologies to generate more evidence.Electronic supplementary materialThe online version of this chapter (doi:10.1007/8904_2014_296) contains supplementary material, which is available to authorized users.
机译:背景:尽管有癫痫发作控制,但由于抗quitinin(ATQ)缺乏导致的吡ido醇依赖性癫痫病(PDE)患者中有百分之七十五患有发育迟缓和/或智力障碍(IQ(<70)。一项观察性研究表明,限制赖氨酸饮食的辅助治疗是安全的,可导致体液中赖氨酸中间体的部分正常化,并可能对癫痫发作控制和精神运动发育产生有益作用。方法:类似于NICE指南过程,国际PDE联盟是一个开放平台,由从事代谢性癫痫领域工作的科学家和临床医生组成,在四个讲习班(2010-2013年)期间制定了关于PDE赖氨酸限制饮食的建议,旨在标准化其实施和监测耐心。此外,建议进行进一步的观察性研究。结果:(1)所有确诊为ATQ缺乏症的患者均符合接受赖氨酸限制性饮食的辅助治疗的条件,除非单独使用吡x醇治疗可完全缓解症状,包括正常行为和发展。 (2)应尽早开始限制赖氨酸;最佳持续时间尚未确定。 (3)饮食应按照这些建议进行,并应监测患者,以确保最佳的护理质量和安全性。讨论:实施该建议将提供一个独特且急需的机会来收集数据完善建议并增进我们对受这种罕见疾病影响的个体的预后的了解。因此,我们提出了一项国际观察性研究,该研究将利用可自由访问的在线数据共享技术来产生更多证据。电子补充材料本章的在线版本(doi:10.1007 / 8904_2014_296)包含补充材料,授权用户可以使用。

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