Degree of Digestibility of Barley Rice Proteins
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 12
- 试验地点
- 2
- 主要终点
- Change in degree of digestibility
研究概览
简要总结
This study aims to assess the degree of digestibility of barley rice protein and compare this to another sustainable, commercially available protein concentrate (pea protein), and a benchmark whey protein, and to assess the effects on blood glucose and insulin levels.
The study is a randomized, cross-over, double blind, controlled trial. Three different treatments, all representing a 20g protein load, will be evaluated with a washout period of minimum one week between the test days. Blood will be collected via a catheter before and up-to five hours after protein consumption. Wellbeing, health complaints or other adverse effects will be collected via a short questionnaire during each test day. After each test day gastrointestinal complaints are collected via an online questionnaire.
详细描述
Barley rice protein is extracted from brewer spent grains (BSG), which is the most voluminous by-product of the brewing industry. Until now, BSG has been mainly used for animal feed or is directly discarded, which is an enormous waste of resources and causes serious environmental pollution. BSG is rich in cellulose and non-cellulosic polysaccharides, lignin, and proteins. The protein fraction of BSG contains a relatively high content of the essential amino acid, lysine, in comparison to other cereal products. Because of its high nutritional content, BSG can be applied in human food products for fortification. The digestion characteristics of barley rice protein are not known, but essential to evaluate their future potential as a sustainable protein source.
The primary objective is to estimate the degree of digestibility of barley rice protein by measuring post-prandial amino acid uptake kinetics, and compare this to pea protein and a benchmark protein (whey).
Secondary objectives are to assess the effects on blood glucose and insulin levels.
The study is a randomized, cross-over, double blind, controlled trial. Three different treatments, all representing a 20g protein load, will be evaluated with a washout period of minimum one week between the test days. Blood will be collected via a catheter before and up-to five hours after protein consumption. Wellbeing, health complaints or other adverse effects will be collected via a short questionnaire during each test day. After each test day gastrointestinal complaints are collected via an online questionnaire.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Other
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
盲法说明
Double (Participant, Investigator)
入排标准
- 年龄范围
- 18 Years 至 40 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Apparently healthy men and women;
- •Age between 18 and 40 years;
- •Body mass index (BMI) between 18.5 and 30 kg/m2 ;
- •Having veins suitable for blood sampling via a catheter (judged by study nurse/ medical doctor).
排除标准
- •Any metabolic, gastrointestinal, inflammatory or chronic disease (such as diabetes, anaemia, hepatitis, cardiovascular disease),or having a condition or disease that may lead to an impaired immune system;
- •History of gastrointestinal surgery or having (serious) gastrointestinal complaints;
- •History of liver dysfunction (cirrhosis, hepatitis) or liver surgery;
- •Kidney dysfunction (self-reported);
- •Any use of medication that may suppress the immune system, this will be judged by the medical supervisor;
- •Use of medication that may influence the study results, such as gastric acid inhibitors, laxatives, stomach protectors and drugs that can affect intestinal motility, this will be judged by the medical supervisor;
- •Anaemia (Hb values <7.5 mmol/L for women and <8.5 mmol/L for men);
- •Reported slimming, medically prescribed or other extreme diets;
- •Use of protein supplements;
- •Not willing to give up blood donation during the study;
- •Current smokers;
- •Alcohol intake ≥4 glasses of alcoholic beverages per day;
- •Pregnant, lactating or wishing to become pregnant in the period of the study (self-reported);
- •Abuse of hard drugs;
- •Having food allergies and/or intolerances (e.g. for gluten);
- •Not having a general practitioner;
- •Participation in another clinical trial at the same time;
- •Being an employee of the department Food, Health & Consumer Research of Wageningen Food & Biobased Research.
结局指标
主要结局
Change in degree of digestibility
时间窗: During the intervention period on 3 test days: at baseline and postprandial blood samples will be collected from the cannula at 10 time points (T=0, 30, 45, 60, 90, 120, 150, 180, 240, 300 minutes)
In order to assess change in the degree of digestibility, we determine 19 free amino acids in blood samples collected via a catheter before and at several time points up-to five hours after protein source consumption. Blood amino acids will be determined by the laboratory of Wageningen FBR, according a valid method: AccQ-Tag ultra-derivation kit \& HPLC.
次要结局
- Change in plasma glucose levels(During the intervention period on 3 test days: at baseline and postprandial blood samples will be collected from the cannula at 10 time points (T=0, 30, 45, 60, 90, 120, 150, 180, 240, 300 minutes))
- Change in plasma insulin levels(During the intervention period on 3 test days: at baseline and postprandial blood samples will be collected from the cannula at 10 time points (T=0, 30, 45, 60, 90, 120, 150, 180, 240, 300 minutes))
研究者
Diederik Esser
Project leader clinical trials
Wageningen University and Research