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Diets high in resistant starch increase plasma levels of trimethylamine-N-oxide a gut microbiome metabolite associated with CVD risk

机译:高抗性淀粉饮食会增加血浆三甲胺-N-氧化物的水平这是一种与CVD风险相关的肠道微生物组代谢产物

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摘要

Production of trimethylamine-N-oxide (TMAO), a biomarker of CVD risk, is dependent on intestinal microbiota, but little is known of dietary conditions promoting changes in gut microbial communities. Resistant starches (RS) alter the human microbiota. We sought to determine whether diets varying in RS and carbohydrate (CHO) content affect plasma TMAO levels. We also assessed postprandial glucose and insulin responses and plasma lipid changes to diets high and low in RS. In a cross-over trial, fifty-two men and women consumed a 2-week baseline diet (41 percentage of energy (%E) CHO, 40% fat, 19% protein), followed by 2-week high- and low-RS diets separated by 2-week washouts. RS diets were assigned at random within the context of higher (51–53 %E) v. lower CHO (39–40 %E) intake. Measurements were obtained in the fasting state and, for glucose and insulin, during a meal test matching the composition of the assigned diet. With lower CHO intake, plasma TMAO, carnitine, betaine and γ-butyrobetaine concentrations were higher after the high- v. low-RS diet (P< 0·01 each). These metabolites were not differentially affected by high v. low RS when CHO intake was high. Although the high-RS meal reduced postprandial insulin and glucose responses when CHO intake was low (P<0·01 each), RS did not affect fasting lipids, lipoproteins, glucose or insulin irrespective of dietary CHO content. In conclusion, a lower-CHO diet high in RS was associated with higher plasma TMAO levels. These findings, together with the absence of change in fasting lipids, suggest that short-term high-RS diets do not improve markers of cardiometabolic health.
机译:CVD风险的生物标志物三甲胺-N-氧化物(TMAO)的产生依赖于肠道菌群,但对于促进肠道微生物群落变化的饮食条件知之甚少。抗性淀粉(RS)会改变人类微生物群。我们试图确定饮食中RS和碳水化合物(CHO)含量的变化是否会影响血浆TMAO水平。我们还评估了高和低RS饮食的餐后葡萄糖和胰岛素反应以及血浆脂质变化。在一项交叉试验中,五十二名男性和女性食用了2周的基线饮食(41%的能量(%E)CHO,40%的脂肪,19%的蛋白质),然后是2周的高,低RS饮食被2周的冲洗分开。在较高(51–53%E)对较低CHO(39–40%E)摄入量的情况下,随机分配RS饮食。在空腹状态下进行测量,并在与指定饮食组成相匹配的进餐测试中获取葡萄糖和胰岛素。 CHO摄入量较低时,高v。低RS饮食后血浆TMAO,肉碱,甜菜碱和γ-丁甜菜碱的浓度较高(每个P <0·01)。当CHO摄入量高时,这些代谢物不受高v。低RS的差异影响。尽管当CHO摄入量低(每次P <0·01)时,高RS餐可降低餐后胰岛素和葡萄糖反应,但无论饮食中的CHO含量如何,RS都不会影响空腹脂质,脂蛋白,葡萄糖或胰岛素。总之,高RS的低CHO饮食与较高的血浆TMAO水平相关。这些发现以及空腹血脂没有变化,表明短期的高RS饮食不能改善心脏代谢健康的指标。

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