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Beta Glucan and Acetate Production

The Effects of Beta Glucan on Acetate Production and Human Substrate Metabolism

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03714646
Enrollment
24
Registered
2018-10-22
Start date
2018-09-05
Completion date
2019-05-10
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity, Pre Diabetes

Brief summary

Based on our hypothesis that orally administered resistant starch and beta glucan will be fermented into a SCFA pattern high in acetate and that this will lead to beneficial effects on human substrate and energy metabolism, we aim to address the following primary objective: To investigate the effects of an acute administration of inulin/beta glucan in combination with resistant starch on fecal and plasma acetate, as well as on fasting and postprandial substrate and energy metabolism in lean normoglycemic men and obese, prediabetic men.

Interventions

DIETARY_SUPPLEMENTbeta glucan and resistant starch

12g per day the day before the CID Resistant starch 7.5 g

DIETARY_SUPPLEMENTPlacebo

isocaloric maltodextrin before the CID

DIETARY_SUPPLEMENTbeta gluten

12 g beta gluten there day before the CID

Sponsors

Maastricht University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
MALE
Age
30 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* lean (BMI ≥ 20kg/m2 and ≤ 24.9kg/m2) * normoglycemic * aged 30 - 65 years OR * overweight/obese (BMI ≥ 25kg/m2 and ≤ 34.9kg/m2) * pre-diabetes * aged between 30 - 65 years.

Exclusion criteria

* diabetes mellitus * gastroenterological diseases or major abdominal surgery (allowed i.e.: ---appendectomy, cholecystectomy) * lactose intolerance and other digestive disorders * cardiovascular disease, cancer, liver or kidney malfunction (determined based on ALAT and creatinine levels, respectively) * disease with a life expectancy shorter than 5 years * Use of antibiotics 3 months prior inclusion * Use of probiotics or prebiotics

Design outcomes

Primary

MeasureTime frame
Plasma acetate concentrations (microM)at baseline (before a high-fat mixed meal)

Secondary

MeasureTime frame
fat oxidation (g/min) will be measured using an open-circuit ventilated hood system (Omnical, Maastricht University, The Netherlands)at baseline and four hours after a high fat mixed meal
carbohydrate oxidation (g/min) will be measured using an open-circuit ventilated hood system (Omnical, Maastricht University, The Netherlands)at baseline and four hours after a high fat mixed meal
Circulating hormone concentrations (Insulin, GLP-1, PYY)at baseline and four hours after a high fat mixed meal
Energy expenditure (kJ/min) will be measured using an open-circuit ventilated hood system (Omnical, Maastricht University, The Netherlands)at baseline and four hours after a high fat mixed meal
Plasma glucose (mmol/L)at baseline and four hours after a high fat mixed meal
Free Fatty Acids (micromol/L)at baseline and four hours after a high fat mixed meal
Breath H2 using (Bedfont EC60 Gastrolyzer, Rochester, UK)at baseline and four hours after a high fat mixed meal
Circulating metabolite concentrations (Glucose, Free Fatty Acids, Triglycerides)at baseline and four hours after a high fat mixed meal

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026