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Clinical Trials/NCT06023940
NCT06023940
Completed
Not Applicable

Variability in Microbial Response to Dietary Fiber

University of Missouri-Columbia1 site in 1 country30 target enrollmentMay 12, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Microbial Colonization
Sponsor
University of Missouri-Columbia
Enrollment
30
Locations
1
Primary Endpoint
Concentration of SCFA
Status
Completed
Last Updated
last year

Overview

Brief Summary

The goal of this clinical trial is to understand varying in responses to different dietary patterns in healthy people who are getting a health screening colonoscopy.

The main questions it aims to answer are:

  • What is the variability in the change of the microbes in the gut of (1) a provided diet that is high in fiber vs (2) a diet of the participant's choice.
  • What is the magnitude of fasting changes in glucose and lipids following the short-term, high-fiber feeding period and identify candidate predictive factors (short-chain fatty acids, BMI, sex, starting glucose level) for these changes

Participants will be in one of two groups:

  1. High-fiber diet group: These participants will have a series of measurements that include: blood biochemistries, body composition measured via DEXA, anthropometrics, surveys and questionnaires, and collection of fecal samples.
  2. Normal diet group: These participants will eat a diet that is of their choosing (ad libitum) and will have a series of measurements that include: fecal samples, and questionnaires/surveys including food records.

Detailed Description

Fiber fermentation in the colon produces short chain fatty acids (SCFA) and alters the microbial composition and activity. These effects may be mechanisms linking a high-fiber diet to improved health. However, different people may respond to dietary fiber differently and the variability in early, dietary-induced SCFA concentration changes has not been established. This lack of basic understanding in individual patterns of microbial SCFA production significantly limits efforts in the field of Precision Nutrition designed to target dietary strategies to improve health and advance lifestyle treatments in healthcare in the future. In this project, the central hypothesis is that the mechanisms by which dietary fiber provide metabolic benefits include a direct physical effect to improve fasting glucose and lipids and an effect related to increasing SCFA concentration. These are the ideas being tested in this study. Using fiber derived from peas in a two-week human feeding intervention, Aim 1 will quantitate the variability in high-fiber-induced change in microbial composition and SCFA production by specifically testing the hypothesis that Following successful colonoscopy bowel prep, variability in the reduction in microbial species will be very small, while repopulation after a standardized high-fiber diet will be characterized by larger differences between individuals with regard to the quantity of bifidobacterial and the Firmicutes/ Bacteroidetes ratio. Aim 2 will quantitate the magnitude of fasting changes in glucose and lipids following the short-term, high-fiber feeding period and identify candidate predictive factors (SCFA, BMI, sex, starting glucose level) for these changes by testing the hypothesis that a two-week, high-fiber diet will result in lower plasma glycemia and triglycerides. Participants (n=30) who have undergone a health-screening colonoscopy (HSC) are fed a high-fiber diet for 14 days. Fecal samples are collected before the colonoscopy and on days 1, 7 and 14 after the colonoscopy during high-fiber feeding. On day 1 and 14, the subject visits the clinical unit for a fasting blood draw (for measurement of glucose, lipids, and plasma SCFA), surveys and questionnaires. A control arm will also be included as part of this study. The purpose of the control arm is to quantitate the variability in microbial composition and SCFA production from an ad libitum diet of participants. Instead of providing a high-fiber diet, the repopulation of the gut microbiome will be observed when participants eat a diet that is of their choosing. A series of food records and fecal samples pre- and post-procedure will be collected. Figure 2 shows the protocol of this arm. Food records will be collected: pre-procedure, days 0 (procedure day), 1, 2, 4, 7, 10, 13. Fecal collection will be collected: pre-procedure, 3, 5, 8, 11, 14. This arm will not include the blood collection or DEXA scan.

Registry
clinicaltrials.gov
Start Date
May 12, 2022
End Date
October 31, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Elizabeth Jane Parks

Professor, Nutrition & Exercise Physiology-MED

University of Missouri-Columbia

Eligibility Criteria

Inclusion Criteria

  • Men and women
  • Age 45-65y: the average age of people referred for a screening colonoscopy
  • BMI ≥20.0 or ≤40.0 kg/m2
  • Weight stable: no fluctuations in body weight of greater than 4 kg in the last 3 months
  • Scheduled for a health-screening colonoscopy
  • Willingness to consume a high-fiber diet
  • Willing to provide blood and fecal samples
  • Healthy or have one or more characteristics of the metabolic syndrome (but not diabetic) Metabolic syndrome criteria
  • A large waistline: 35 inches or more for women 40 inches or more for men
  • High triglycerides: 150 mg/dL or higher

Exclusion Criteria

  • Pregnant or lactating, or planning to become pregnant
  • BMI of \<20.0 or \>40.0 kg/m2
  • Use of tobacco products
  • Uncontrolled hypertension and blood pressure ≥ 180/110
  • Use of medications that affect the gut microbiome (e.g., antibiotics)
  • Taking medications known to affect appetite (phentermine) or gastrointestinal function (e.g. metformin)
  • On a special diet vegetarian, or other restricted dietary patterns
  • Undergoing weight loss
  • Ad libitum intake of fiber above 25 g/day (mean intake in the US population is 17 g/day) and also an intake of fiber \<10 g/d
  • Ad libitum alcohol intake of greater than 7 drinks/week for women and 14 drinks/week for men

Outcomes

Primary Outcomes

Concentration of SCFA

Time Frame: 2 weeks

Measured via fecal sample. Intervention group - measured once before scheduled health screening colonoscopy and 2 times over 2 weeks post-colonoscopy (day 1, 7, 14). Control group - measured once before scheduled health screening colonoscopy and 5 days over 2 weeks post-colonoscopy (day 3, 5, 8, 11, 14).

Variability in microbial composition as measured by 'alpha diversity'

Time Frame: 2 weeks

Measured via fecal sample. Intervention group - measured once before scheduled health screening colonoscopy and 2 times over 2 weeks post-colonoscopy (day 1, 7, 14). Control group - measured once before scheduled health screening colonoscopy and 5 days over 2 weeks post-colonoscopy (day 3, 5, 8, 11, 14). Variability in microbial composition refers to how many different kinds of microbes are present in the fecal sample. We are testing the possibility that the more kinds of microbes, the healthier the person. The higher the measure the alpha diversity, the greater the number of different microbes.

Secondary Outcomes

  • Blood glucose concentration (mg/dL)(2 weeks)
  • Blood lipid concentation (total cholesterol, LDLc, HDLc) (mg/dL)(2 weeks)

Study Sites (1)

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