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采用改良的地中海生酮饮食可逆转人类阿尔茨海默病的外周脂质特征。

Consuming a modified Mediterranean ketogenic diet reverses the peripheral lipid signature of Alzheimer's disease in humans.

作者信息

Neth Bryan J, Huynh Kevin, Giles Corey, Wang Tingting, Mellett Natalie A, Duong Thy, Blach Colette, Schimmel Leyla, Register Thomas C, Blennow Kaj, Zetterberg Henrik, Batra Richa, Schweickart Annalise, Dilmore Amanda Hazel, Martino Cameron, Arnold Matthias, Krumsiek Jan, Han Xianlin, Dorrestein Pieter C, Knight Rob, Meikle Peter J, Craft Suzanne, Kaddurah-Daouk Rima

机构信息

Department of Neurology, Mayo Clinic, Rochester, MN, USA.

Baker Heart and Diabetes Institute, 75 Commercial Road, Melbourne, VIC, Australia.

出版信息

Commun Med (Lond). 2025 Jan 9;5(1):11. doi: 10.1038/s43856-024-00682-w.

Abstract

BACKGROUND

Alzheimer's disease (AD) is a major neurodegenerative disorder with significant environmental factors, including diet and lifestyle, influencing its onset and progression. Although previous studies have suggested that certain diets may reduce the incidence of AD, the underlying mechanisms remain unclear.

METHOD

In this post-hoc analysis of a randomized crossover study of 20 elderly adults, we investigated the effects of a modified Mediterranean ketogenic diet (MMKD) on the plasma lipidome in the context of AD biomarkers, analyzing 784 lipid species across 47 classes using a targeted lipidomics platform.

RESULTS

Here we identified substantial changes in response to MMKD intervention, aside from metabolic changes associated with a ketogenic diet, we identified a a global elevation across all plasmanyl and plasmenyl ether lipid species, with many changes linked to clinical and biochemical markers of AD. We further validated our findings by leveraging our prior clinical studies into lipid related changeswith AD (n = 1912), and found that the lipidomic signature with MMKD was inversely associated with the lipidomic signature of prevalent and incident AD.

CONCLUSIONS

Intervention with a MMKD was able to alter the plasma lipidome in ways that contrast with AD-associated patterns. Given its low risk and cost, MMKD could be a promising approach for prevention or early symptomatic treatment of AD.

摘要

背景

阿尔茨海默病(AD)是一种主要的神经退行性疾病,饮食和生活方式等重要环境因素会影响其发病和进展。尽管先前的研究表明某些饮食可能降低AD的发病率,但其潜在机制仍不清楚。

方法

在对20名老年人进行的随机交叉研究的事后分析中,我们在AD生物标志物的背景下研究了改良地中海生酮饮食(MMKD)对血浆脂质组的影响,使用靶向脂质组学平台分析了47类中的784种脂质。

结果

在此我们发现,除了与生酮饮食相关的代谢变化外,MMKD干预还引起了显著变化,我们发现所有缩醛磷脂和缩醛磷脂醚脂质种类均出现整体升高,且许多变化与AD的临床和生化标志物相关。我们通过利用之前关于AD脂质相关变化的临床研究(n = 1912)进一步验证了我们的发现,发现MMKD的脂质组学特征与现患和新发AD的脂质组学特征呈负相关。

结论

MMKD干预能够以与AD相关模式相反的方式改变血浆脂质组。鉴于其低风险和低成本,MMKD可能是预防或早期对症治疗AD的一种有前景的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/116a/11711287/398c6d7d20cf/43856_2024_682_Fig1_HTML.jpg

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