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临床试验/NCT05260762
NCT05260762已完成不适用

Personalized Obesity Management - Matching Dietary Fibers and Microbial Enterotype (POMFAME)

University of Copenhagen2 个研究点 分布在 1 个国家目标入组 95 人开始时间: 2022年4月13日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
95
试验地点
2
主要终点
Body weight change

研究概览

简要总结

The overall aim of this 12-week randomized controlled trial is to investigate if a dietary fiber supplement rich in arabinoxylans (AX) affects weight loss success differently according to baseline gut microbiota composition in subjects who have overweight or obesity.

105 participants will be randomized in a 2:1 ratio to receive 15 g/day of AX or placebo.

详细描述

First, we hypothesize that participants who have a predominantly Prevotella enterotype (inferred by a high Prevotella/Bacteroides-ratio) will lose more body weight after AX supplementation compared to participants with a predominantly Bacteroides enterotype (inferred by a low Prevotella/Bacteroides-ratio). Specifically, we hypothesize that weight loss and P/B-ratio will be positively correlated in the AX supplementation-group whereas there will be no such correlation in the control-group. Consequently, we hypothesize that participants with the Bacteroides enterotype - and the lowest P/B-ratio - will have no benefit after AX supplementation while the weight loss effect of the AX supplementation will increase with increasing P/B-ratio.

Second, we hypothesize that the ability to digest starch in the upper gastrointestinal tract - evaluated by salivary alpha amylase gene (AMY1) copy number - will influence the interactions among AX intake, P/B ratio, and body weight change. Specifically, we hypothesize that there will be an association between body weight change and P/B ratio among subjects with a low AMY1 copy number, but not among the ones with a high AMY1 copy number, when consuming AX.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
20 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Apparently healthy men or women (self-reported nonpregnant, nonlactating, and not planning a pregnancy in the next 4 months)
  • BMI: 25 to 40 kg/m2
  • Non-smoker
  • Want to maintain or lose weight
  • Willing to consume wheat buns on a daily basis

排除标准

  • Consumption of whole grain products with every meal
  • Use of antibiotics 60 days prior to the start of the study. If a participant uses antibiotics prior to randomization, they will be invited to be re-screened 3 months after the last use of antibiotics, provided that it is realistic to complete the study no later than the scheduled LPLV
  • Dietary supplements with pro- and/or prebiotics 6 weeks prior to study
  • Self-reported eating disorders
  • Being a bodybuilder (>4 strength training sessions per week)
  • Alcohol intake above the recommendation from the Danish Health and Medicines Authority (>21 units of alcohol per week)
  • Night- or shift work
  • Chronic diseases e.g. cancer within the past 5 years (except adequately-treated localized basal cell skin cancer), asthma, thyroid disease, cardiovascular disease, type 1 or 2 diabetes, inflammatory diseases, and celiac disease
  • Disorders: neurological, sleep, diagnosed psychiatric disorder and gastrointestinal and liver disorders
  • Surgical treatment of obesity and abdominal surgery
  • Inability, physically or mental, to comply with the procedures required by the study protocol as evaluated by the daily study manager, principal investigator or clinical responsible
  • Subject's general condition contraindicates continuing the study as evaluated by the daily study manager, principal investigator or clinical responsible
  • Simultaneous blood donation for another purpose than this study
  • Simultaneous participation in other clinical intervention studies

结局指标

主要结局

Body weight change

时间窗: Baseline to week 12

Weight will be measured using a calibrated digital scale,in kg to the nearest 0.1 kg

次要结局

  • Blood glucose metabolism(Baseline to week 12)
  • Fecal microbiota composition(Baseline to week 12)
  • Body fat change(Baseline to week 12)
  • Resting energy expenditure(Baseline to week 12)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Faidon Magkos

Associate professor

University of Copenhagen

研究点 (2)

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