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

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Bryan J Neth, Kevin Huynh, Corey Giles, Tingting Wang, Natalie A Mellett, Thy Duong, Colette Blach, Leyla Schimmel, Thomas C Register, Kaj Blennow, Henrik Zetterberg, Richa Batra, Annalise Schweickart, Amanda Hazel Dilmore, Cameron Martino, Matthias Arnold, Jan Krumsiek, Xianlin Han, Pieter C Dorrestein, Rob Knight, Peter J Meikle, Suzanne Craft, Rima Kaddurah-Daouk
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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.

食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。
背景:阿尔茨海默病(AD)是一种主要的神经退行性疾病,饮食和生活方式等环境因素对其发病和进展有重要影响。尽管先前的研究表明,某些饮食可能会降低AD的发病率,但其潜在机制尚不清楚。方法:在这项随机交叉研究的20名老年人的事后分析中,我们研究了改良的地中海生酮饮食(MMKD)对AD生物标志物背景下血浆脂质组的影响,使用靶向脂质组学平台分析了47类784种脂质。结果:在这里,我们发现了对MMKD干预的实质性变化,除了与生酮饮食相关的代谢变化外,我们还发现了所有浆蛋白基和浆蛋白基醚类脂质的全球升高,其中许多变化与AD的临床和生化标志物有关。我们进一步验证了我们的发现,利用我们之前的临床研究脂质与AD相关的变化(n = 1912),发现MMKD的脂质组学特征与流行和偶发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。由于其低风险和低成本,MMKD可能是一种有希望的预防或早期对症治疗AD的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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