Supplementation of Diet With Galacto-oligosaccharides Increases Bifidobacteria, but Not Insulin Sensitivity, in Obese Prediabetic Individuals

被引:156
作者
Canfora, Emanuel E. [1 ,2 ]
van der Beek, Christina M. [1 ,3 ]
Hermes, Gerben D. A. [1 ,4 ]
Goossens, Gijs H. [1 ,2 ]
Jocken, Johan W. E. [1 ,2 ]
Holst, Jens J. [5 ,6 ]
van Eijk, Hans M. [3 ]
Venema, Koen [1 ,7 ]
Smidt, Hauke [1 ,4 ]
Zoetendal, Erwin G. [1 ,4 ]
Dejong, Cornelis H. C. [1 ,3 ,8 ]
Lenaerts, Kaatje [1 ,3 ]
Blaak, Ellen E. [1 ,2 ]
机构
[1] Top Inst Food & Nutr, Wageningen, Netherlands
[2] Maastricht Univ, Med Ctr, NUTRIM Sch Nutr & Translat Res Metab, Dept Human Biol, Maastricht, Netherlands
[3] Maastricht Univ, Med Ctr, NUTRIM Sch Nutr & Translat Res Metab, Dept Surg, Maastricht, Netherlands
[4] Wageningen Univ, Lab Microbiol, Wageningen, Netherlands
[5] Univ Copenhagen, Ctr Basic Metab Res, Novo Nordisk Fdn, Copenhagen, Denmark
[6] Univ Copenhagen, Panum Inst, Dept Biomed Sci, Copenhagen, Denmark
[7] Beneficial Microbes Consultancy, Wageningen, Netherlands
[8] Univ Klinikum Aachen, Dept Surg, Aachen, Germany
关键词
Short-Chain Fatty Acids; Prebiotics; Microbial Obesity; Metabolic Control; CHAIN FATTY-ACIDS; CHROMATOGRAPHY-MASS SPECTROMETRY; MIXTURE B-GOS; GUT-MICROBIOTA; FECAL MICROBIOTA; IMMUNE FUNCTION; DOUBLE-BLIND; BODY-WEIGHT; HEALTH; METABOLISM;
D O I
10.1053/j.gastro.2017.03.051
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: The gut microbiota affects host lipid and glucose metabolism, satiety, and chronic low-grade inflammation to contribute to obesity and type 2 diabetes. Fermentation end products, in particular the short-chain fatty acid (SCFA) acetate, are believed to be involved in these processes. We investigated the long-term effects of supplementation with galacto-oligosaccharides (GOS), an acetogenic fiber, on the composition of the human gut microbiota and human metabolism. METHODS: We performed a double-blinded, placebo- controlled, parallel intervention study of 44 overweight or obese (body mass index, 28-40 kg/m(2)) prediabetic men and women (ages, 45-70 y) from October 2014 through October 2015 in Maastricht, The Netherlands. The participants were assigned randomly to groups who ingested 15 g GOS or isocaloric placebo (maltodextrin) dailywith their regular meals for 12 weeks. Before and after this period, we collected data on peripheral and adipose tissue insulin sensitivity, fecal microbiota composition, plasma and fecal SCFA, energy expenditure and substrate oxidation, body composition, and hormonal and inflammatory responses. The primary outcome was the effect of GOS on peripheral insulin sensitivity, measured by the hyperinsulinemic-euglycemic clamp method. RESULTS: Supplementation of diets with GOS, but not placebo, increased the abundance of Bifidobacterium species in feces by 5-fold (P =.009; q = 0.144). Microbial richness or diversity in fecal samples were not affected. We did not observe any differences in fecal or fasting plasma SCFA concentrations or in systemic concentrations of gut-derived hormones, incretins, lipopolysaccharide-binding protein, or other markers of inflammation. In addition, no significant alterations in peripheral and adipose tissue insulin sensitivity, body composition, and energy and substrate metabolism were found. CONCLUSIONS: Twelve-week supplementation of GOS selectively increased fecal Bifidobacterium species abundance, but this did not produce significant changes in insulin sensitivity or related substrate and energy metabolism in overweight or obese prediabetic men and women. ClincialTrials.gov number, NCT02271776.
引用
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页码:87 / +
页数:14
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