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生酮饮食疗法治疗阿尔茨海默病:最新综述。

Ketogenic diet therapy in Alzheimer's disease: an updated review.

机构信息

Université de Paris.

INSERM UMRS1144 Optimisation Thérapeutique en Neuropsychopharmacologie.

出版信息

Curr Opin Clin Nutr Metab Care. 2021 Jul 1;24(4):372-378. doi: 10.1097/MCO.0000000000000759.

Abstract

PURPOSE OF REVIEW

Ketogenic diets (KD) are validated treatments of pharmacoresistant epilepsy. Their interest in neurodegenerative diseases such as Alzheimer's disease (AD) has been suggested, because ketone bodies may reduce neuroinflammation, improve neurotransmitters transport pathway, synaptic maintenance, and reduce brain β-amyloid deposition. In this updated review, we aimed at critically examining the evidence of the past 2 years regarding KD or ketogenic supplements (KS) on cognitive and biological/neuropathological outcomes. We conducted our search in preclinical studies (animal models of AD) or in humans with or without cognitive impairment.

RECENT FINDINGS

Overall, 12 studies were included: four in animal models of AD and eight in humans. In preclinical studies, we found additional evidence for a decrease in cerebral inflammation as well as in specific features of AD: β-amyloid, aggregates of tau protein under KD/KS. Several AD mouse models experienced clinical improvements. Human studies reported significant cognitive benefits, improved brain metabolism and biomarkers change under KD/KS, despite rather short-term interventions. Adherence to KD or KS was acceptable with frequent, but minor gastrointestinal adverse effects.

SUMMARY

The present review gathered additional evidence for both pathophysiological and clinical benefits of KS/KD in AD. Further studies are warranted with a biomarker-based selection of AD participants and long-term follow-up.

摘要

目的综述

生酮饮食(KD)是治疗耐药性癫痫的有效方法。生酮饮食对神经退行性疾病(如阿尔茨海默病,AD)的作用已被证实,因为酮体可能减轻神经炎症、改善神经递质转运途径、突触维持并减少脑β-淀粉样蛋白沉积。在本次更新的综述中,我们旨在批判性地检查过去 2 年关于 KD 或生酮补充剂(KS)对认知和生物学/神经病理学结果的证据。我们的检索范围包括临床前研究(AD 动物模型)和有或没有认知障碍的人类研究。

最新发现

共纳入 12 项研究:4 项 AD 动物模型研究和 8 项人类研究。在临床前研究中,我们发现 KD/KS 可进一步减轻脑炎症以及 AD 的特定特征:β-淀粉样蛋白、tau 蛋白聚集。一些 AD 小鼠模型出现了临床改善。人类研究报告了 KD/KS 对认知的显著益处,改善了大脑代谢和生物标志物变化,尽管干预时间较短。KD 或 KS 具有良好的耐受性,仅有频繁但轻微的胃肠道不良反应。

总结

本综述为 KS/KD 在 AD 中的病理生理和临床益处提供了更多证据。需要进一步研究,包括基于生物标志物的 AD 患者选择和长期随访。

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