Variability in Microbial Response to Dietary Fiber

NCT ID: NCT06023940

Last Updated: 2024-07-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-05-12
• Study Completion Date: 2023-10-31

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.

Conditions

Microbial Colonization

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

High Fiber

Subjects are provided a high-fiber diet for 2 weeks. Tests include: blood biochemistries, body composition measured via DEXA, fecal sample collection, and anthropometrics measured

Group Type: EXPERIMENTAL

High fiber

Intervention Type: DIETARY_SUPPLEMENT

A pea fiber supplement is added to a diet of regular foods. Participants receive 25g fiber daily.

Control

Subjects are not provided any diet, instead they eat what they choose for two weeks while they participate in a series of tests including: fecal sampling, food records, questionnaires/surveys, and anthropometrics

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

High fiber

A pea fiber supplement is added to a diet of regular foods. Participants receive 25g fiber daily.

Intervention Type: DIETARY_SUPPLEMENT

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

1. A large waistline: 35 inches or more for women 40 inches or more for men

2. High triglycerides: 150 mg/dL or higher

3. Low HDLc level: <50 mg/dL for women <40 mg/dL for men

4. High blood pressure ≥130/85 mmHg

5. Fasting blood sugar ≥100 mg/dL - Pre-diabetes acceptable (glucose <125 mg/dL or HbA1c <6.5%)

• Subjects are also eligible if they are stably treated with statin drugs, anti-hypertensive medications, and anti-depressants. These are eligible as long as the drug category does not alter appetite, body weight, or the microbiome (if known).

• Men and women
• Age 45-65y: the average age of people referred for a screening colonoscopy
• Scheduled for a health-screening colonoscopy
• Willing to provide fecal samples
• Subjects are also eligible if they are stably treated with statin drugs, anti-hypertensive medications, and anti-depressants. These are eligible as long as the drug category does not alter appetite, body weight, or the microbiome (if known).

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
• History of disease (example colon cancer, etc.)
• Live more than 45 miles away from the University because participants will need to come into the Lab every 3 days or so to pick up meals.

• Pregnant or lactating, or planning to become pregnant
• Use of medications that affect the gut microbiome (e.g., antibiotics within the past 30 days)
• History of disease (example colon cancer, active GI bleeding, inflammatory bowel disease, etc.)
• Live more than 45 miles away from the University because participants will need to come into the Lab every 3 days or so to deliver fecal samples.

• Minimum Eligible Age: 45 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of Missouri-Columbia

OTHER

Sponsor Role: lead

Responsible Party

Elizabeth Jane Parks

Professor, Nutrition & Exercise Physiology-MED

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Elizabeth Parks

Role: PRINCIPAL_INVESTIGATOR

University of Missouri-Columbia

Yezaz Ghouri, MD

Role: PRINCIPAL_INVESTIGATOR

University of Missouri-Columbia

Katherene Anguah, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Missouri-Columbia

Locations

University of Missouri

Columbia, Missouri, United States

Countries

United States

Other Identifiers

2053546

Identifier Type: -

Identifier Source: org_study_id