一项随机、安慰剂对照、单中心、交叉研究,评估餐前乳清蛋白微凝胶对2型糖尿病和超重或肥胖患者餐后糖代谢和氨基酸反应的影响。

IF 3.7 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Metabolites Pub Date : 2025-01-16 DOI:10.3390/metabo15010061
Ian J Neeland, Luiz H de Gregório, Roberto Zagury, Bo Ahrén, Joel Neutel, Christian Darimont, John Corthesy, Yohan Grzywinski, Emilie Perrin, Maximilian von Eynatten, Odd Erik Johansen
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Effects on PPG (primary endpoint), insulin, GLP-1, and branched-chain amino acids (BCAAs) were evaluated with frequent blood sampling. Changes in incremental areas under the concentration curve (iAUC) were compared using a mixed model. <b>Results</b>: Twenty-six individuals (14 females, mean ± SD age 62.0 ± 8.3 years, HbA1c 58 ± 12 mmol/mol/7.5 ± 1.1%, BMI 29.2 ± 4.8 kg/m<sup>2</sup>) completed both tests. WPM significantly reduced PPG iAUC<sub>0-2h</sub> by 22% (<i>p</i> = 0.028), and iAUC<sub>0-3h</sub> numerically by -18% (<i>p</i> = 0.090) vs. placebo. WPM also increased insulin iAUC<sub>0-1h</sub> by 61% (<i>p</i> < 0.001), and iAUC<sub>0-3h</sub> by 30% (<i>p</i> = 0.004), respectively. Total GLP-1 iAUC<sub>0-2h</sub> was enhanced by 66% (<i>p</i> < 0.001). Postprandial plasma BCAA patterns were characterized by a rapid increase and larger iAUC<sub>0-2h</sub> (all <i>p</i> < 0.001) after WPM. 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引用次数: 0

摘要

目的:餐前摄入乳清蛋白(WP)通过刺激内源性GLP-1分泌和胰岛素来抑制食欲和降低餐后葡萄糖(PPG)。方法:我们使用一种新的胶束技术(WPM)评估了浓缩WP对2型糖尿病(T2D)和超重或肥胖(NCT04639726)患者的代谢影响。在随机交叉设计中,参与者间隔7±4天进行两次240分钟午餐(622千卡)测试。经过一夜禁食和标准化早餐后,在混合营养餐前15分钟饮用10克(125毫升)WPM(40千卡)或安慰剂(125毫升水,0千卡)。通过频繁采血评估对PPG(主要终点)、胰岛素、GLP-1和支链氨基酸(BCAAs)的影响。采用混合模型比较浓度曲线下增量面积的变化。结果:26例(女性14例,平均±SD年龄62.0±8.3岁,HbA1c 58±12 mmol/mol/7.5±1.1%,BMI 29.2±4.8 kg/m2)完成了两项检测。与安慰剂相比,WPM显著降低PPG iAUC0-2h 22% (p = 0.028), iAUC0-3h数值降低-18% (p = 0.090)。WPM组胰岛素iAUC0-1h升高61% (p < 0.001), iAUC0-3h升高30% (p = 0.004)。总GLP-1 iAUC0-2h升高66% (p < 0.001)。餐后血浆BCAA模式的特点是WPM后快速升高和较大的iAUC0-2h(均p < 0.001)。没有不良事件归因于食用WPM。结论:在混合餐前饮用125 mL含10 g WPM的餐前饮料可降低PPG并增加胰岛素、GLP-1和支链氨基酸。因此,WPM可能在伴有超重或肥胖的T2D患者中作为代谢调节剂。
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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A Randomized, Placebo-Controlled, Single-Center, Crossover Study to Evaluate the Effects of Pre-Meal Whey Protein Microgel on Post-Prandial Glucometabolic and Amino Acid Response in People with Type 2 Diabetes and Overweight or Obesity.

Purpose: Whey protein (WP) consumption prior to a meal curbs appetite and reduces postprandial glucose (PPG) through stimulating endogenous GLP-1 secretion and insulin. Methods: We assessed the metabolic effects of a concentrated WP, using a new micelle-technology (WPM), in people with type 2 diabetes (T2D) and overweight or obesity (NCT04639726). In a randomized-crossover design, participants performed two 240 min lunch meal (622 kcal) tests 7 ± 4 days apart. After an overnight fast and a standardized breakfast, 10 g (125 mL) WPM (40 kcal) or placebo (125 mL water, 0 kcal) was consumed 15 min ahead of the mixed-nutrient meal. Effects on PPG (primary endpoint), insulin, GLP-1, and branched-chain amino acids (BCAAs) were evaluated with frequent blood sampling. Changes in incremental areas under the concentration curve (iAUC) were compared using a mixed model. Results: Twenty-six individuals (14 females, mean ± SD age 62.0 ± 8.3 years, HbA1c 58 ± 12 mmol/mol/7.5 ± 1.1%, BMI 29.2 ± 4.8 kg/m2) completed both tests. WPM significantly reduced PPG iAUC0-2h by 22% (p = 0.028), and iAUC0-3h numerically by -18% (p = 0.090) vs. placebo. WPM also increased insulin iAUC0-1h by 61% (p < 0.001), and iAUC0-3h by 30% (p = 0.004), respectively. Total GLP-1 iAUC0-2h was enhanced by 66% (p < 0.001). Postprandial plasma BCAA patterns were characterized by a rapid increase and larger iAUC0-2h (all p < 0.001) after WPM. No adverse events were ascribed to consuming WPM. Conclusions: A 125 mL pre-meal drink containing just 10 g WPM before a mixed meal reduced PPG and increased insulin, GLP-1, and BCAAs. WPM may therefore serve as a metabolic modulator in people with T2D living with overweight or obesity.

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来源期刊
Metabolites
Metabolites Biochemistry, Genetics and Molecular Biology-Molecular Biology
CiteScore
5.70
自引率
7.30%
发文量
1070
审稿时长
17.17 days
期刊介绍: Metabolites (ISSN 2218-1989) is an international, peer-reviewed open access journal of metabolism and metabolomics. Metabolites publishes original research articles and review articles in all molecular aspects of metabolism relevant to the fields of metabolomics, metabolic biochemistry, computational and systems biology, biotechnology and medicine, with a particular focus on the biological roles of metabolites and small molecule biomarkers. Metabolites encourages scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on article length. Sufficient experimental details must be provided to enable the results to be accurately reproduced. Electronic material representing additional figures, materials and methods explanation, or supporting results and evidence can be submitted with the main manuscript as supplementary material.
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