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Why Calories Are Not the Same - a Gut Explanation?

Not Applicable
Not yet recruiting
Conditions
Diet, Healthy
Breath Analysis
Registration Number
NCT06932666
Lead Sponsor
University of Copenhagen
Brief Summary

The aim of this study is to understand how the gut microbiome influences how much dietary energy humans excrete via feces. This study is based on the hypothesis that levels of methane in exhaled breath represent two different gut microbiome community structures, and therefore influence fecal energy excretion differently. Moreover, this study is assessed in the context of two different diets, both isocaloric and equal in macronutrient composition, but differing in contents of fiber, resistant starch, and large particles; which are hypothesized to impact the gut microbiome differently.

Detailed Description

The trial is a cross-over trial including two controlled isocaloric dietary interventions of three days duration. The two diets are isocaloric but with different contents of fiber, resistant starch, and food particle sizes. Each intervention is separated by a wash-out period of at least 10 days where participants adhere to their habitual diet. The trial includes a total of five visits (one screening visit and four regular visits).

Before the trial, participants undergo a screening period of 4 days. During the 4-day screening period, participants measure the levels of methane in their exhaled breath. Based on median breath methane levels, participants are allocated to one of the two arms: (HMP: high methane producers; LMP: low methane producers). Enrollment in the intervention trial will be conducted so there are similar numbers of participants in both arms.

At the beginning and at the end of each 3-day intervention period, participants consume a blue muffin, containing a royal blue dye that changes the stool color. The appearance of the color in stool following the first muffin will mark the beginning of the stool collection period, which will continue until the stool color change is no longer noticeable following consumption of the second muffin. Therefore, the duration of the stool collection period, which is estimated to be on average 3 days, will ultimately depend on the participants' passage time of food (i.e., intestinal transit time).

During the screening period, participants are asked to:

* measure their methane and hydrogen levels in exhaled breath using a portable device

* report defecation patterns (including stool frequency and Bristol Stool Scale)

Before each intervention period, participants are asked to:

* collect a fecal and urine sample

* register three days of habitual diet

At the visits before each intervention period, the following samples are collected:

* a blood sample

* methane and hydrogen measurements in exhaled breath

* anthropometrics

* data on physical activity

During the intervention periods, participants are asked to:

* exclusively eat all the foods provided

* collect all their stool samples, as specified above

* collect three morning urine samples (one daily for the following three days)

* measure their methane and hydrogen levels in their exhaled breath using a portable device

* report their defecation patterns and gastrointestinal symptoms

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • 18-65 years old
  • BMI:18.5-29.9 kg/m2
  • Self-reported regular defecations defined as at least every second day
  • Willing to collect urine and stool samples at home and able to temporarily store them in their own freezer in a provided container
  • Willing to exclusively eat the food provided
  • Owning a smartphone (iOS 11.0 and onwards, or Android 5.0 and onwards) with access to the internet
  • Speak and understand Danish or English
Exclusion Criteria
  • Current pregnancy or lactation
  • Following a specific dietary program or diet (e.g., vegetarian, vegan, gluten-free) or unable to consume the food provided
  • Diagnosis of small intestinal bacterial overgrowth (SIBO), inflammatory bowel diseases (IBD), gastrointestinal obstruction, or ischemic colitis
  • Diagnosed chronic constipation
  • Regular use of diarrhea inhibitors or laxatives
  • Any chronic disease that can affect the outcomes of the study
  • Use of medications potentially altering gastric pH (proton pump inhibitors, histamine receptor antagonists, antacids)
  • Use of medications potentially altering the gastro-intestinal motility (prokinetics, antiemetic agents, anticholinergic agents, narcotic analgesics, nonsteroidal anti-inflammatory drugs, peroral glucocorticoids, and GLP-1 related medications such as semaglutide and liraglutide)
  • Use of antibiotics, or any medication that can affect any outcomes of the study, within the previous three months
  • Concurrent participation in another trial
  • Any condition that makes the project responsible and/or the clinical responsible doubt the feasibility of the volunteer's participation

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Primary Outcome Measures
NameTimeMethod
Total fecal energy excretion (between high- and low-methane producers)During each stool collection period (following each 3-day intervention period)

Differences in total fecal energy excretion, determined as total kilocalories excreted via feces, between low and high methane producers following intake of the two controlled, isocaloric diets.

Secondary Outcome Measures
NameTimeMethod
Total fecal energy excretion (between diet A and diet B)During each stool collection period (following each 3-day intervention period)

Differences in total fecal energy excretion, determined as total kilocalories excreted via feces, between the two isocaloric diets (that differ in fiber, resistant starch, and particle size).

Fecal energy densityDuring each 3-day intervention period and its following stool collection period

Differences in fecal energy density, determined as fecal energy (kcal) relative to fecal weight, between high- and low-methane producers.

Breath hydrogen and methane levelsDuring each 3-day intervention period and its following stool collection period

Differences in breath methane and hydrogen concentration in exhaled breath, measured in parts per million (PPM), between high- and low-methane producers.

Whole-gut transit timeDuring each 3-day intervention period and its following stool collection period

Differences in whole-gut transit time, determined by the passage time of muffins with blue dye, between high- and low-methane producers.

Stool consistencyDuring each 3-day intervention period and its following stool collection period

Differences in stool consistency, determined by Bristol Stool Scale, between high- and low-methane producers.

Stool frequencyDuring each 3-day intervention period and its following stool collection period

Differences in stool frequency, determined by defecation records registered by the participants, between high- and low-methane producers.

Fecal pHDuring each 3-day intervention period and its following stool collection period

Differences in fecal pH between high- and low-methane producers.

Stool moistureDuring each 3-day intervention period and its following stool collection period

Differences in stool moisture, determined as fecal water content relative to fecal weight, between high- and low-methane producers.

Fecal microbial loadDuring each 3-day intervention period and its following stool collection period

Differences in fecal microbial load, determined as total microbial DNA reads in feces, between high- and low-methane producers.

Fecal host DNA concentrationDuring each 3-day intervention period and its following stool collection period

Differences in fecal host DNA concentration, determined as total human DNA reads in feces, between high- and low-methane producers.

Fecal short-chain fatty acidsDuring each 3-day intervention period and its following stool collection period

Differences in fecal short-chain fatty acid concentrations between high- and low-methane producers.

Gut microbiome composition (16S)During each 3-day intervention period and its following stool collection period

Differences in gut microbiome composition, determined by 16S amplicon sequencing of fecal DNA, between high- and low-methane producers.

Gut microbiome composition and functions (shotgun sequencing)During each 3-day intervention period and its following stool collection period

Differences in gut microbiome taxonomic composition and functions, determined by shotgun sequencing of fecal DNA, between high- and low-methane producers.

Trial Locations

Locations (1)

University of Copenhagen, Department of Nutrition, Exercise and Sports

🇩🇰

Frederiksberg C, Capital Region, Denmark

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