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Epilepsy Behav Rep. 2019 Dec 19;13:100353. doi: 10.1016/j.ebr.2019.100353. eCollection 2020.
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Ketogenic Diet and Breast Cancer: Recent Findings and Therapeutic Approaches.生酮饮食与乳腺癌:最新研究发现与治疗方法。
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本文引用的文献

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Outpatient initiation of the ketogenic diet in children with pharmacoresistant epilepsy: An effectiveness, safety and economic perspective.门诊启动生酮饮食治疗儿童耐药性癫痫:有效性、安全性和经济学角度。
Eur J Paediatr Neurol. 2019 Sep;23(5):740-748. doi: 10.1016/j.ejpn.2019.06.001. Epub 2019 Jun 29.
2
Modified ketogenic diets in adults with refractory epilepsy: Efficacious improvements in seizure frequency, seizure severity, and quality of life.改良生酮饮食治疗成人耐药性癫痫:有效改善发作频率、发作严重程度和生活质量。
Epilepsy Behav. 2019 Apr;93:113-118. doi: 10.1016/j.yebeh.2018.12.010. Epub 2019 Mar 10.
3
Understanding the core principles of a 'modified ketogenic diet': a UK and Ireland perspective.了解“改良型生酮饮食”的核心原则:英国和爱尔兰的观点。
J Hum Nutr Diet. 2019 Jun;32(3):385-390. doi: 10.1111/jhn.12637. Epub 2019 Mar 11.
4
Overall cognitive profiles in patients with GLUT1 Deficiency Syndrome.GLUT1 缺乏综合征患者的整体认知特征。
Brain Behav. 2019 Mar;9(3):e01224. doi: 10.1002/brb3.1224. Epub 2019 Feb 4.
5
Use of the Modified Atkins Diet in Intractable Pediatric Epilepsy.改良阿特金斯饮食在难治性小儿癫痫中的应用。
J Epilepsy Res. 2018 Jun 30;8(1):20-26. doi: 10.14581/jer.18004. eCollection 2018 Jun.
6
Practice Paper of the Academy of Nutrition and Dietetics: Classic and Modified Ketogenic Diets for Treatment of Epilepsy.营养与饮食学会练习题:用于治疗癫痫的经典及改良生酮饮食
J Acad Nutr Diet. 2017 Aug;117(8):1279-1292. doi: 10.1016/j.jand.2017.06.006.
7
Use of dietary therapies amongst patients with GLUT1 deficiency syndrome.葡萄糖转运蛋白1缺乏综合征患者的饮食疗法应用
Seizure. 2016 Feb;35:83-7. doi: 10.1016/j.seizure.2016.01.011. Epub 2016 Jan 14.
8
The Effects of Ketogenic Diet on Seizures, Cognitive Functions, and Other Neurological Disorders in Classical Phenotype of Glucose Transporter 1 Deficiency Syndrome.生酮饮食对葡萄糖转运蛋白1缺乏综合征经典型患者癫痫发作、认知功能及其他神经系统疾病的影响
Neuropediatrics. 2015 Oct;46(5):313-20. doi: 10.1055/s-0035-1558435. Epub 2015 Aug 12.
9
Glucose transporter type 1 deficiency syndrome effectively treated with modified Atkins diet.1型葡萄糖转运体缺乏综合征经改良阿特金斯饮食有效治疗。
Neuropediatrics. 2014 Apr;45(2):117-9. doi: 10.1055/s-0033-1349225. Epub 2013 Jul 25.
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An update on diets in clinical practice.临床实践中饮食的最新情况。
J Child Neurol. 2013 Aug;28(8):1015-26. doi: 10.1177/0883073813487597. Epub 2013 May 14.

改良阿特金斯饮食法,碳水化合物缓慢减少。

Modified Atkins Diet with slow reduction of carbohydrate.

作者信息

Gauthier Amanda, Simic Nevena, Jones Kevin C, RamachandranNair Rajesh

机构信息

Niagara Health, Welland, Ontario, Canada.

Comprehensive Pediatric Epilepsy Program, McMaster Children's Hospital, Hamilton, Ontario, Canada.

出版信息

Epilepsy Behav Rep. 2019 Dec 19;13:100353. doi: 10.1016/j.ebr.2019.100353. eCollection 2020.

DOI:10.1016/j.ebr.2019.100353
PMID:32337504
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7176585/
Abstract

Typically, the amount of daily carbohydrate in the Modified Atkins diet (MAD) is restricted to 10-20 g from the beginning of the therapy. It is possible to gradually reduce the daily carbohydrate amount to this target to increase acceptability of the diet. We report the use of the MAD with slow carbohydrate reduction in a patient with Glucose Transporter 1 Deficiency, including results of neuropsychological assessments. Seizures were controlled at 45 g of carbohydrates daily. This case report illustrates that a liberalized form of MAD with slow reduction of carbohydrate may be a therapeutic option in some children with epilepsy. It is possible that other children with epilepsy could achieve seizure control at higher carbohydrate level than current MAD recommendations.

摘要

通常,改良阿特金斯饮食(MAD)从治疗开始时起,每日碳水化合物摄入量就限制在10 - 20克。可以逐渐将每日碳水化合物量减少至该目标,以提高饮食的可接受性。我们报告了在一名葡萄糖转运蛋白1缺乏症患者中使用缓慢减少碳水化合物的MAD,包括神经心理学评估结果。癫痫发作在每日45克碳水化合物时得到控制。本病例报告表明,一种碳水化合物缓慢减少的宽松形式的MAD可能是一些癫痫患儿的治疗选择。其他癫痫患儿有可能在高于当前MAD建议的碳水化合物水平时实现癫痫发作控制。