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Metabolic Effects of a 24-Week Energy-Restricted Intervention Combined with Low or High Dairy Intake in Overweight Women: An NMR-Based Metabolomics Investigation

机译:超重女性的24周能量受限干预与低或高乳制品摄入量相结合的代谢影响:基于NMR的代谢组学研究

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摘要

We investigated the effect of a 24-week energy-restricted intervention with low or high dairy intake (LD or HD) on the metabolic profiles of urine, blood and feces in overweight/obese women by NMR spectroscopy combined with ANOVA-simultaneous component analysis (ASCA). A significant effect of dairy intake was found on the urine metabolome. HD intake increased urinary citrate, creatinine and urea excretion, and decreased urinary excretion of trimethylamine-N-oxide (TMAO) and hippurate relative to the LD intake, suggesting that HD intake was associated with alterations in protein catabolism, energy metabolism and gut microbial activity. In addition, a significant time effect on the blood metabolome was attributed to a decrease in blood lipid and lipoprotein levels due to the energy restriction. For the fecal metabolome, a trend for a diet effect was found and a series of metabolites, such as acetate, butyrate, propionate, malonate, cholesterol and glycerol tended to be affected. Overall, even though these effects were not accompanied by a higher weight loss, the present metabolomics data reveal that a high dairy intake is associated with endogenous metabolic effects and effects on gut microbial activity that potentially impact body weight regulation and health. Moreover, ASCA has a great potential for exploring the effect of intervention factors and identifying altered metabolites in a multi-factorial metabolomic study.
机译:我们通过NMR光谱法与ANOVA同时成分分析相结合,研究了低或高乳制品摄入量(LD或HD)的24周能量受限干预对超重/肥胖女性尿液,血液和粪便代谢谱的影响( ASCA)。发现摄入乳制品对尿液代谢组有显着影响。相对于LD摄入量,HD摄入量增加了柠檬酸,肌酐和尿素的排泄,降低了三甲胺-N-氧化物(TMAO)和马尿酸盐的尿排泄,这表明HD摄入量与蛋白质分解代谢,能量代谢和肠道微生物活性的改变有关。 。另外,对血液代谢组的显着时间影响归因于由于能量限制而使血脂和脂蛋白水平降低。对于粪便代谢组,发现了饮食效应的趋势,并且一系列代谢产物,例如乙酸盐,丁酸盐,丙酸盐,丙二酸盐,胆固醇和甘油趋向于受到影响。总体而言,即使这些影响并没有带来更高的体重减轻,目前的代谢组学数据显示,高乳制品摄入量与内源性代谢作用以及对肠道微生物活动的影响有关,这可能会影响体重调节和健康。此外,在多因素代谢组学研究中,ASCA在探索干预因素的作用和鉴定改变的代谢产物方面具有巨大潜力。

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