FIBFLO——一项比较饮食对微生物组及其代谢影响的研究设计:是否为β-葡聚糖?

E. Norin, L. Engstrand, P. Hellström, L. Martin Marais, T. Midtvedt, R. Möllby, I. Ernberg
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引用次数: 0

摘要

已经证实,人类肠道微生物组是共生的,有助于消化我们的食物,并参与肠道的代谢过程以及免疫系统的发育和维持。[1] 微生物组及其基因处理我们吃的主要未消化的食物,并传递代谢产物,这些代谢产物经常被我们的血液和微生物群吸收。据估计,我们血浆中10%的小代谢产物来自微生物代谢。然而,直到最近,人们才普遍接受它对人类健康和疾病发展的重要性。这在很大程度上取决于高通量测序方法的可用性,该方法允许使用高效且具有成本效益的工具来识别肠道微生物组成员的部分,以及它们可能如何受到环境扰动的影响。[2-4]人类微生物组是一种很有前途的资产,是疾病风险的早期生物标志物,也是饮食和非侵入性治疗干预的目标。在生理条件下可能影响肠道微生物群(GM)组成和功能的所有因素中,饮食是迄今为止最重要的,也是最容易用来操纵GM的因素。[5-7]在这种情况下,燕麦是一种独特且具有挑战性的饮食成分。β-葡聚糖是一种线性混合葡萄糖聚合物,其葡萄糖残基通过β-1–3(约30%)和β-1–4键(约70%)连接。[8] 体外发酵研究[8,9]以及体内动物研究的结果证明了燕麦对转基因的影响。[8-12]尽管食用燕麦对健康有很好的促进作用,但可以合理地假设,对人类的多方面研究可能会揭示食用燕麦对人类健康的新益处,可能也会在个体层面上。本研究被设计为建立多学科方法的试点研究,包括拟人化、微生物组、代谢组学的收集和评估,在一项双盲交叉研究中,一组健康成年志愿者在规定的时间内每天接受含或不含燕麦β-葡聚糖的预制餐,其免疫学和肠道相关功能数据。[13,14]目的是评估肠道微生物、生化和免疫参数的测试系统,以确定β-葡聚糖纤维对健康志愿者肠道微生物群组成和功能的影响。通过广告招募了20名男性。研究中只包括男性的原因是在第一次筛查中尽量避免激素影响和其他外部因素。这项研究是一项双盲调查,每组包括10名志愿者。最初,他们由临床医生(PH)检查健康状况,包括是否存在可能影响微生物群功能的因素,如抗菌药物。在饮食干预之前、期间和之后,收集血液、尿液和粪便进行分析,同时,参与者吞下一粒“智能药丸”。[15] 此外,参与者还填写了关于饥饿和饱腹感、布里斯托尔量表、胃肠道症状和健康状况的问卷。每个研究周期持续两周。
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FIBFLO – a study design for comparing the effects of diets on the microbiome and its metabolism: β-glucan or not?
It has been established that the human gut microbiome is commensal, helps to digest our food, and is involved in metabolic processes in the gut and in the development and maintenance of our immune systems.[1] The microbiome and its genes process the primarily indigested food we eat and deliver metabolites, which frequently are taken up in our blood and by our microbiota. An estimated 10% of the small metabolites in our blood plasma are derived from microbial metabolism. However, only recently there has been a general acceptance of its importance for human development in health and disease. This depends largely on the availability of high-throughput sequencing methods which allows efficient and cost-effective tools to identify parts of the members of the gut microbiome and how they might be affected by environmental perturbations.[2–4] The human microbiome is a promising asset as an early biomarker for disease risks and a target for dietary and non-invasive therapeutic interventions. Among all factors which, under physiological conditions, might affect the composition and function of gut microbiota (GM), diet is by far the most important and is also the easiest factor to use in order to manipulate the GM.[5–7] In this context, oats represent a unique and challenging dietary ingredient. Much attentions have been focused on its content of β-glucan which is a linear mixed glucose polymer with glucose residues linked via beta-1–3 (about 30%) and beta-1–4 linkages (around 70%).[8] Results from in vitro fermentation studies [8,9] as well as in vivo animal studies demonstrate effects of oats on GM. [8–12] In spite of all the promising health-promoting effect of oats consumption, it is reasonable to assume that multifaceted studies in humans may uncover new human-health benefits of oats consumption, maybe also on an individual level. The present investigation was designed as a pilot study for establishing a multi-disciplinary approach, including collection and evaluation of anthropomorphic, microbiomic, metabolomics, immunological and gut-related functional data in a cohort of healthy adult volunteers daily receiving a pre-made meal with or without oat β-glucan for a defined period of time in a double-blinded cross-over study.[13,14] The aim was to evaluate a test system of intestinal microbiological, biochemical and immunological parameters to determine the effects of β-glucan fiber on composition and function of human intestinal microbiota in healthy volunteers. Twenty males were recruited by advertisement. The reason for including only men in the study was to try to avoid hormone influences and other external factors in this first screening. The study was a double blinded investigation including 10 volunteers per group. Initially, they were examined by a clinician (PH) for health status including absence of factors that could influence microbiota functions, e.g. antimicrobials. Before, during and after the dietary intervention, blood, urine and feces were collected for analyses and at the same time, the participants swallowed a ‘smart pill’.[15] Moreover, the participants filled in questionnaires regarding hunger and satiety, Bristol scale, gastrointestinal symptoms and wellbeing. Each study period lasted for two weeks.
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