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生酮饮食和低脂饮食对阿尔茨海默病高危成年人的代谢组、微生物组和食物组的影响。

Effects of a ketogenic and low-fat diet on the human metabolome, microbiome, and foodome in adults at risk for Alzheimer's disease.

机构信息

Department of Pediatrics, University of California San Diego, La Jolla, California, USA.

Biomedical Sciences Graduate Program, University of California San Diego, La Jolla, California, USA.

出版信息

Alzheimers Dement. 2023 Nov;19(11):4805-4816. doi: 10.1002/alz.13007. Epub 2023 Apr 5.

DOI:10.1002/alz.13007
PMID:37017243
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10551050/
Abstract

INTRODUCTION

The ketogenic diet (KD) is an intriguing therapeutic candidate for Alzheimer's disease (AD) given its protective effects against metabolic dysregulation and seizures. Gut microbiota are essential for KD-mediated neuroprotection against seizures as well as modulation of bile acids, which play a major role in cholesterol metabolism. These relationships motivated our analysis of gut microbiota and metabolites related to cognitive status following a controlled KD intervention compared with a low-fat-diet intervention.

METHODS

Prediabetic adults, either with mild cognitive impairment (MCI) or cognitively normal (CN), were placed on either a low-fat American Heart Association diet or high-fat modified Mediterranean KD (MMKD) for 6 weeks; then, after a 6-week washout period, they crossed over to the alternate diet. We collected stool samples for shotgun metagenomics and untargeted metabolomics at five time points to investigate individuals' microbiome and metabolome throughout the dietary interventions.

RESULTS

Participants with MCI on the MMKD had lower levels of GABA-producing microbes Alistipes sp. CAG:514 and GABA, and higher levels of GABA-regulating microbes Akkermansia muciniphila. MCI individuals with curcumin in their diet had lower levels of bile salt hydrolase-containing microbes and an altered bile acid pool, suggesting reduced gut motility.

DISCUSSION

Our results suggest that the MMKD may benefit adults with MCI through modulation of GABA levels and gut-transit time.

摘要

简介

鉴于生酮饮食 (KD) 对代谢失调和癫痫有保护作用,它是阿尔茨海默病 (AD) 的一种很有前途的治疗候选药物。肠道微生物群对于 KD 介导的抗癫痫作用以及胆汁酸的调节至关重要,胆汁酸在胆固醇代谢中起主要作用。这些关系促使我们分析了在与低脂饮食干预相比的受控 KD 干预后与认知状态相关的肠道微生物群和代谢物。

方法

患有前驱糖尿病的成年人,无论是有轻度认知障碍 (MCI) 还是认知正常 (CN),都接受低脂美国心脏协会饮食或高脂肪改良地中海 KD (MMKD) 治疗 6 周;然后,经过 6 周的洗脱期后,他们交叉到另一种饮食。我们在五个时间点收集粪便样本进行 shotgun 宏基因组学和非靶向代谢组学分析,以研究个体在整个饮食干预过程中的微生物组和代谢组。

结果

接受 MMKD 的 MCI 参与者的 GABA 产生菌 Alistipes sp. CAG:514 和 GABA 水平较低,而 GABA 调节菌 Akkermansia muciniphila 水平较高。饮食中含有姜黄素的 MCI 个体的胆汁盐水解酶含量较高的微生物和胆汁酸池发生改变,表明肠道蠕动减少。

讨论

我们的结果表明,MMKD 可能通过调节 GABA 水平和肠道转运时间使 MCI 成年人受益。

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