Prevention of Diabetes with a Novel Butyrate-enriched Triglyceride
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 48
- 试验地点
- 2
- 主要终点
- Peripheral insulin sensitivity
研究概览
简要总结
A body of animal studies as well as observational studies in humans demonstrated that butyrate is one SCFA that has pronounced positive effects on body weight control, inflammation, and insulin resistance. Even though the SCFA hexanoate is less researched, it has been shown to be involved in anti-inflammatory processes. Of note, acute human studies showed that fibre-induced metabolic improvements are linked to higher SCFA levels in the systemic circulation. It has been shown that a butyrate/hexanoate-enriched triglyceride oil enhanced systemic butyrate and hexanoate concentrations for a prolonged time. Yet, it remains to be determined whether a chronic increase in circulating butyrate and hexanoate concentrations translate into long-term benefits. In this study it is hypothesized that a chronic increase of butyrate/hexanoate in the circulation may improve host metabolism and metabolic health by improving adipose tissue function, reducing systemic lipid overflow and inflammation thereby increasing peripheral insulin sensitivity in individual with overweight/obesity and prediabetes.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Basic Science
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 20 Years 至 70 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •In order to be eligible to participate in this study, a subject must meet all of the following criteria:
- •Age 20-70 years
- •BMI ≥ 28 and < 40 kg/m2
- •Weight stable for at least 3 months
- •Normal blood pressure (systolic blood pressure 100-140 mmHg, diastolic blood pressure 60-90 mmHg)
- •One or more of the following criteria to determine disturbed glucose/insulin homeostasis
- •Fasting glucose 5.6-6.9 mmol/L
- •Two-hour glucose of 7.8-11.1 mmol/L
- •HOMA-IR ≥ 2.2
- •HbA1c (5.7-6.4%)
排除标准
- •Diabetes mellitus (type 1 or 2)
- •Cardiovascular disease: including no history or myocardial infarction, heart failure, arrhythmias
- •Pulmonary disease: no history of chronic obstructive pulmonary disease, emphysema, bronchitis, asthma
- •Kidney (e.g. kidney failure) or liver (e.g. cirrhosis, non-alcoholic fatty acid) malfunction
- •Gastrointestinal disease (no inflammatory bowel disease, irritable bowel syndrome or digestive disorders) or a history of abdominal surgery (except appendectomy and cholecystectomy)
- •Autoimmune disease
- •Any other diseases affecting glucose and/or lipid metabolism or use of any medication that influence glucose or fat metabolism and inflammation
- •Ongoing disease or any disease with a life expectancy ≤ 5 years
- •Abuse of products; alcohol (>15 units per week) and drugs, excessive nicotine use defined as >20 cigarettes per week
- •Regular supplementation of pre- or probiotic products, use of pre- or probiotics, antibiotics and laxatives 3 months prior to the start of the study
- •Intensive exercise training more than three hours a week
- •Plan to lose weight or to follow a hypocaloric diet or vegetarian diet
- •Pregnancy
结局指标
主要结局
Peripheral insulin sensitivity
时间窗: Before and 6 months after the start of the intervention
The change of peripheral insulin sensitivity as assessed by a hyperinsulinaemic-euglycemic clamp
次要结局
- circulating SCFA(Before and 6 months after the start of the intervention)
- hepatic insulin sensitivity(Before and 6 months after the start of the intervention)
- Substrate oxidation (indirect calorimetry)(Before and 6 months after the start of the intervention)
- Faecal SCFA(Before and 6 months after the start of the intervention)
- Faecal microbiota composition(Before and 6 months after the start of the intervention)
- body weight(Before and 6 months after the start of the intervention)
- adipose tissue insulin sensitivity(Before and 6 months after the start of the intervention)
- Energy expenditure (indirect calorimetry)(Before and 6 months after the start of the intervention)
- body composition(Before and 6 months after the start of the intervention)
- Circulating hormones such as insulin(Before and 6 months after the start of the intervention)
- Circulating metabolites such as glucose(Before and 6 months after the start of the intervention)
- Gut permeability(Before and 6 months after the start of the intervention)