Batch Fermentation and Microbiome Analysis
Study Details
Study Description
Brief Summary
The correlation between diet and microbiota as well as the effect of microbiota on human health is well established. Studies have shown that people following specific diets have different microbiome profile compared to those following traditional or ordinary diets. In order to screen several food ingredients for their effects on human microbiota composition and metabolic activities, in vitro studies are proposed. Nutrients are added in-vitro in fecal sample, eliminating the need for participants to consume any nutritional product. The batch fermentation in vitro system simulates human colonic microbiota from fecal samples, enabling the complex mixture of microorganisms. This system could serve as a simple model to simulate the diversity as well as the metabolism of human colonic microbiota. We will evaluate the effect on nutrient/s on the age specific microbiome via an in vitro fermentation approach for the 0 to 60 year-old period.
| Condition or Disease | Intervention/Treatment | Phase |
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Study Design
Outcome Measures
Primary Outcome Measures
- Change in microbiota composition [Through study completion, an average of 1 year]
Measured by 16s rRNA sequencing or next Generation Sequencing (NGS) or by qPCR
Secondary Outcome Measures
- Change in Short Chain Fatty Acids (SCFA) [Through study completion, an average of 1 year]
Measured using Gas Chromatography (GC)
- Change in metabolic profile [Through study completion, an average of 1 year]
Measured using Gas Chromatography (GC) or Gas chromatography-mass spectrometry (GC-MS)
- Protein expression of epithelial cells [Through study completion, an average of 1 year]
Measured by western blot
Eligibility Criteria
Criteria
Inclusion Criteria:
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Healthy participant aged from 0 to 60 (based on medical history, physical examination and review of childhood growth chart)
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Written informed consent has been obtained from the parent(s)/legally acceptable representative (LAR) of toddlers and teenagers
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Written informed consent has been obtained for participants aged from 14 years old and above
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Child's parent(s)/legal representative or participant is willing and able to fulfill the requirements of the study protocol.
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Ability to collect their or their infant/child's fecal sample.
Exclusion Criteria:
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The parent(s)/legally acceptable representative (LAR) is not able to provide evidence of parental authority or legal representation.
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Participant following a particular regimen of any type such as vegan, vegetarian, ketogenic, paleo diet,
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Chronic or recurrent diarrhea with spontaneous bowel movements more often than 2 times daily,
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Antibacterial/antifungal therapy during the 3 months prior to study enrolment,
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Medications or supplements that are known to alter gut function or microbiota (i.e. acid antisecretory drugs, pre-/probiotics supplements, laxatives) during the 4 weeks prior to study enrolment,
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Prior gastrointestinal surgery (apart from appendectomy, cholecystectomy or herniotomy),
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Alcohol intake higher than 2 servings per day. A serving is 0.4 dl of strong alcohols, 1 dl of red or white wine, or 3 dl of beer,
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Artificially sweetened beverage intake higher than 1000 ml/ per day,
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Current or history of gastrointestinal diseases like (Celiac Disease, Crohn's Disease, Ulcerative colitis, Irritable Bowel Syndrome, infantile colic, recurrent abdominal pain, functional constipation, ulcers, infections (based on anamnesis),
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Participants participating in another interventional study,
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Participants/parents having a hierarchical or family link with the research team members.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Nestle Clinical Innovation Lab | Lausanne | Vaud | Switzerland | 1000 |
Sponsors and Collaborators
- Société des Produits Nestlé (SPN)
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 1920NR