Fiber Fermentation, and Short Chain Fatty Acid Kinetics and Utilization Inside the Gut and Systemic Circulation

Dietary Fiber Clinical Trial

Official title:

A Feasibility Study on Fiber Fermentation, and Short Chain Fatty Acid Kinetics and Utilization Inside the Gut and Systemic Circulation

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04499183
• Other study ID #: NL74418.081.20
• Status: Recruiting
• Phase: N/A
• Start date: October 8, 2020
• Est. completion date: February 1, 2021

Study information

• Verified date: October 2020
• Source: Wageningen University
• Contact: MARA VAN TRIJP
• Phone: 0317 484 067
• Email: mara.vantrijp[@]wur.nl
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Nowadays there is a strong interest in optimising human health through manipulation of non-digestible carbohydrates (NDC). NDC can be used as substrates by gut microbiota, which results in NDC degradation, production of fermentation products, such as short-chain fatty acids (SCFA), and a shift in microbiome composition and activity. It is hypothesized that SCFAs mediate parts of the beneficial effects of NDC. In mice, the influx of SCFA into the host correlated strongly with improvements of markers of the metabolic syndrome, in contrast to the concentrations of SCFA in the proximal colon. Therefore, the influx of short chain fatty acids (SCFA) into the body may be of high importance in improving metabolism. There is a need for more studies in humans to trace the life course of SCFA and their regulatory role in human metabolism. To study this inner world of bacterial products in humans, we will use a nasal-intestine catheter that can be used for delivery of components and sampling chyme in the proximal colon. Before the proposed methodology can be applied in a large intervention study, a small scale feasibility study needs to be performed that addresses colonic placement of the nasal-intestine cathether and colonic sampling of regular and NDC-enriched chyme samples. We will investigate the acute fermentation of fructo- and galacto-oligosaccharides in the proximal colon. Moreover, we will deliver 13C-labelled SCFA via a naso-intestinal catheter to quantify the fluxes of SCFA production, interconversion and uptake by the host. A small-scale, 7-day parallel feasibility trial, N=5 subjects will receive GOS/FOS supplements (mix 1:1 ratio, 15 gram/day), and N=5 other subjects will receive placebo supplements (isocaloric maltodextrin, 12 gram/day). At the last day of the supplementation period, the catheter will be placed, and afterwards participants stay maximum 5 hours in the hospital, to ensure progression of the nose-intestine catheter. After an overnight fast, subjects will visit the hospital again for measurements. Subjects will consume a NDC bolus (200 mL tap water, 5 gram fructo-oligosaccharides, 5 gram galacto-oligosaccharides, non-absorbable marker (PEG-4000). Afterwards, they are not allowed to eat for 6.5 hours. Isotopically 13C-labelled SCFAs will be delivered in the proximal colon. Blood and colonic luminal samples, breath samples, faeces and urine will be collected.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 10
• Est. completion date: February 1, 2021
• Est. primary completion date: February 1, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 60 Years

Eligibility

Inclusion criteria:

• Males
• Age 18-60yrs
• BMI between 18.5 and 30 kg/m2
• Regular bowel movement (defaecation on average once a day)
• Signed informed consent

Exclusion criteria:

• Having a history of medical or surgical events that, in the opinion of the Investigator, may either put the subject at risk because of participation in the study, or influence the results of the study (e.g. diabetes, cardiovascular disease, gastrointestinal disease, renal failure, cancer, infectious disease, nose/throat).
• Having a history of surgical events of the gastro-intestinal tract (e.g. bariatric surgery/gastric bypass surgery)
• Presence of swallowing disorder
• Use of any prescribed or non-prescribed medication (other than paracetamol) including antacids, analgesics, and herbal remedies during the three (3) weeks prior to study start.
• Being lactose intolerant
• Follows a vegan diet
• Use of antibiotics within 3 months of starting the study or planned during the study
• Use of pro- or prebiotics (e.g. galacto-oligosaccharides, fructo-oligosaccharides)
• Constipation/infrequent bowel movement (less than 3 times defaecation per week)
• Abuse of drugs/alcohol (alcohol: >4 consumptions/day or >21 consumptions/week)
• Smoker
• Having diarrhoea within 1 month prior to the study start
• Personnel of Wageningen University, Division of Human Nutrition, their partner and their first and second degree relatives
• Participation in another biomedical study or other research from the Division of Human Nutrition
• Not willing to be exposed to fluoroscopy
• Having a hemoglobin of <8.5 mmol/L
• Having blood vessels that are too difficult for inserting a cannula
• Not having a general practitioner

Related Conditions & MeSH terms

• Dietary Fiber

Intervention

Dietary Supplement:
• fructo- and galacto-oligosaccharides
15 gram/day fructo- and galacto-oligosaccharides

Locations

Country	Name	City	State
Netherlands	Wageningen University and Research	Wageningen

Sponsors (1)

Lead Sponsor	Collaborator
Wageningen University

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Concentrations of non-digestible markers	TiO2 and PEG-4000 inside the intestine	Between 0 and 400 minutes
Primary	Concentrations of carbohydrates	mono-, di-, tri-, oligo- and polysaccharides in the intestinal lumen	Between 0 and 400 minutes
Primary	Relative microbiota composition and metabolites	Microbiota and metabolites inside the intestine	Between 0 and 400 minutes
Primary	Concentrations of plasma metabolites	organic acids, amino acids, glucose, cholesterol, fatty acids and bile acids in blood	Between 0 and 400 minutes
Primary	Catheter placement in the colon	To show placement of a naso-intestinal catheter in the proximal colon.	After 1 week
Primary	Volume of colon sample (mL)	To check whether enough material for analysis is obtained if the catheter system takes samples in the proximal colon of participants.	Between 0 and 400 minutes
Primary	Concentrations of SCFAs	(13C isotopic) enrichments of SCFAs inside intestinal lumen	Between 0 and 400 minutes
Secondary	Concentrations of urine metabolites	hippurate, di- en tri-methylamine, acetaldehydes, taurine, glycine, glucuronic acid conjugates, and bile acid profiles (conjugates)	After 0 and 120 minutes
Secondary	Questionnaires about (dis)comfort of study procedures	Questions about study procedures	After 1 week
Secondary	Relative microbiota composition and metabolite concentrations	Microbiota and metabolome in faeces	After 1 week