Role of Gastrointestinal Microbes on Digestion of Resistant Starch and Tryptophan Availability to Humans

Type II Diabetes Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02974699
• Other study ID #: 110116M1F
• Status: Recruiting
• Phase: Early Phase 1
• First received: November 21, 2016
• Last updated: May 1, 2017
• Start date: January 2017

Study information

• Verified date: May 2017
• Source: Wayne State University
• Contact: Paul R Burghardt, PhD
• Phone: 3135770107
• Email: paul.burghardt[@]wayne.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

There is currently a critical gap in knowledge of how intestinal bacterial communities alter metabolic substrates available to the host thereby influencing central and enteric nervous system (CNS/ENS) neurotransmitter levels involved in regulating carbohydrate consumption in humans. Understanding these relationships is essential for developing strategies to improve blood glucose control and to reduce the risk of transitioning from prediabetes to type-2 diabetes (T2D). The investigators' long-term goal is to determine the biological underpinnings of behaviors that impact food intake and blood glucose control that contribute to the development of T2D. The objective of this proposal, which is an essential next step in attaining the investigators' long-term goals, is to determine how bacterial populations in the digestive system impact circulating tryptophan (TRP) and large neutral amino acid (LNAA) levels that regulate production of monoamine 5-hydroxytryptamine (5-HT, serotonin) in the ENS and in gastrointestinal system and the brain. The central hypothesis is that a reduced ratio of TRP producing (TRPp) to TRP consuming (TRPc) bacteria (decreased TRPp:TRPc ratio) in the gut will decrease TRP availability following a carbohydrate meal lowering the plasma TRP:LNAA ratio and resulting in less TRP for ENS/CNS production of 5HT. Further, dietary interventions that promote TRPp bacterial abundance within the gut will increase TRP availability to the host. The investigators will test the central hypothesis and, thereby, accomplish the overall objective for this project by pursuing the following specific aims: 1) Assess impact of divergent microbiota on plasma TRP:LNAA ratio in response to acute carbohydrate consumption, and 2) Assess the impact of dietary supplementation with resistant starch (RS) on gut microbiota and circulating TRP:LNAA ratio. During Aim 1, stool samples will be collected from healthy participants. Participants will be stratified based on gut TRPp:TRPc ratio and the response to an acute meal will be assessed by determining plasma TRP:LNAA ratios. During Aim 2 the capacity for 4-weeks of pre-biotic RS (Potato Starch) supplementation to increase the TRPp:TRPc bacterial ratio in the gut will be determined from stool samples. Additionally, plasma TRP:LNAA ratio following acute carbohydrate consumption before and after supplementation will be determined. The scientific contribution will be to determine the impact of RS on TRPp and TRPc bacteria abundance in the gut, and how bacterial populations impact circulating TRP:LNAA levels, that can impact ENS and CNS 5HT production in humans. This contribution will be significant because it will have direct translational implications for human diseases with altered 5HT signaling.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 20
• Est. primary completion date: December 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Male and female

2. Age 18 - 65 years old

3. Non-Obese (BMI = 30 kg/m2 and >17 kg/m2 )

Exclusion Criteria:

1. Urine toxicology positive,

2. Pregnant (female)

3. Alcohol intake 48 hours prior to studies,

4. Evidence of inherited disorders of lipid metabolism,

5. History of Cancer within the last 5 years,

6. Human immunodeficiency virus (HIV) antibody positive,

7. Patients with solid organ transplants,

8. Unstable angina or NY heart association class II failure or above,

9. Gastrointestinal disease specifically GI motility disorders,

10. Unstable neuropsychiatric disease including major depression/anxiety, eating disorder such as bulimia or anorexia,

11. End stage renal or hepatic disease,

12. Autoimmune disorders (e.g. SLE),

13. Prior bariatric surgery,

14. A history or current alcohol/substance abuse or nicotine containing products or illicit drugs of abuse during the preceding 6 months,

15. Treatment within one month with sedative hypnotic medications (benzodiazepines, barbiturates), or over the counter sleeping aids

16. Women: any selective estrogen receptor modulator or aromatase inhibitor Men:

androgen ablation/deprivation hormonal therapies

17. Any medical condition, which in the opinion of the investigator would make the patient unsuitable for recruitment, or could interfere with the patient participating in or completing the protocol

18. Any previous adverse events or allergic reactions to acetaminophen

19. Unwilling or unable to consent for the study.

Related Conditions & MeSH terms

• Diabetes Mellitus, Type 2
• Type II Diabetes

Intervention

Dietary Supplement:
• Potato Starch (Bob's Red Mill)
Subjects will be assigned to Potato Starch (active) following assessment of their gut microbiome.
• Pregelatinized Starch (Resource ThickenUp)
Subjects will be assigned to Pregelatinized Starch (placebo) following assessment of their gut microbiome.

Locations

Country	Name	City	State
United States	Wayne State University	Detroit	Michigan

Sponsors (1)

Lead Sponsor	Collaborator
Wayne State University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Plasma Amino Acid Levels		Baseline
Primary	Plasma Amino Acid Levels		Following 4 weeks of supplementation
Secondary	Change in Plasma Amino Acid Levels	Difference in plasma amino acid levels between baseline and following 4-weeks of supplementation	Baseline vs. 4-weeks