Investigation of the Gut Microbiota in Regulating Nutrient Absorption in Humans

Study Results

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

27 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-01-14

Study Completion Date

2019-03-29

Brief Summary

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We propose to study both stool and urine energy loss in 24 individuals on two experimental diets (50% increased and 50% reduced nutrient load relative to body size) in a random cross-over design. Following this over/underfeeding, volunteers will also be randomly assigned to a placebo versus oral antibiotic medication arm. This study will extend our previous findings by investigating whether 1) nutrient absorption changes upon similar increases/decreases in relative nutrient load and 2) whether manipulation of gut microbial communities with antibiotics alters nutrient absorption and 3) how these changes may affect glucose tolerance and fat storage.

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Detailed Description

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The prevalence of obesity has risen to epidemic proportions in the world, resulting from both excessive energy intake and low levels of energy expenditure. The effect of nutrient absorption on energy balance, that is, the relative amount of nutrients consumed vs. the amount excreted in stool, has been reported only in small studies in which energy waste in feces and urine between lean and obese individuals was not found to be different. New studies have shown that bacteria in the gut may play an important role in calorie absorption. We have recently shown that leaner individuals absorbed more calories when overfed compared to when they were given a diet with just enough calories to maintain their own weight. Our studies have also found that overfeeding also changes the kinds of bacteria found in the gut. In lean individuals, these changes in gut bacterial communities with overfeeding were associated with changes in how many calories were absorbed. Our results are similar to those seen in other studies in animals and humans that suggest a role for gut bacteria in weight gain and obesity. To try to better understand the role of gut bacteria in absorbing food, we propose to investigate 1) whether energy loss (as measured in stool and urine) changes following over- and underfeeding relative to body size and 2) whether changes in the gut bacteria, induced by an antibiotic medication, affect nutrient absorption and glucose tolerance. We plan to study 24 healthy non-smoking volunteers age 18 45 years old, not taking any medications (including medications for weight loss, antibiotics or probiotics) for the examination. All participants will be admitted to the Clinical Research Unit for 31 days. During their stay, subjects will be fed a weight maintaining diet for 3 days, followed by two experimental diets (150% and 50% of weight maintaining calories) in a random order. After this, volunteers will be randomly assigned to one of two groups: group 1 will take oral antibiotic medication; group 2 will receive pills that look the same but will not contain any active medication (placebos). Feces (stool) will be collected throughout the study. Additionally, twenty four-hour urine collections will take place each day of the experimental diet period and when stool is collected on the antibiotics. The energy content of these waste products as well as that of the diet (using duplicate plate analysis) will be measured by bomb calorimetry. Bacterial components in feces will be extracted by repeated fractional centrifugation to obtain bacterial mass and by using 16S rDNA-based oligonucleotide probes to obtain data on gut bacteria. Primary results will examine how many calories remain in stool during relative over- and underfeeding and whether changes in gut bacteria, induced by an antibiotic medication, affect nutrient absorption and glucose tolerance.

Conditions

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Obesity

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

PREVENTION

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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OF_UF Vancomycin

Healthy volunteers assigned overfeeding diet, underfeeding diet, and then vancomycin

Group Type EXPERIMENTAL

Vancomycin

Intervention Type DRUG

Vancomycin 125mg orally four times per day for 12 days

Overfeeding diet (OF)

Intervention Type OTHER

Diet in which the calories are 150% of their weight maintaining energy requirements

Underfeeding diet (UF)

Intervention Type OTHER

Diet in which the calories are 50% of their weight maintaining energy requirements

OF_UF Placebo

Healthy volunteers assigned overfeeding diet, underfeeding diet, and then placebo

Group Type PLACEBO_COMPARATOR

Placebo oral tablet

Intervention Type DRUG

Placebo pills orally four times per day for 12 days

Overfeeding diet (OF)

Intervention Type OTHER

Diet in which the calories are 150% of their weight maintaining energy requirements

Underfeeding diet (UF)

Intervention Type OTHER

Diet in which the calories are 50% of their weight maintaining energy requirements

UF_OF Vancomycin

Healthy volunteers assigned underfeeding diet, overfeeding diet, and then vancomycin

Group Type EXPERIMENTAL

Vancomycin

Intervention Type DRUG

Vancomycin 125mg orally four times per day for 12 days

Overfeeding diet (OF)

Intervention Type OTHER

Diet in which the calories are 150% of their weight maintaining energy requirements

Underfeeding diet (UF)

Intervention Type OTHER

Diet in which the calories are 50% of their weight maintaining energy requirements

UF_OF Placebo

Healthy volunteers assigned underfeeding diet, overfeeding diet, and then placebo

Group Type PLACEBO_COMPARATOR

Placebo oral tablet

Intervention Type DRUG

Placebo pills orally four times per day for 12 days

Overfeeding diet (OF)

Intervention Type OTHER

Diet in which the calories are 150% of their weight maintaining energy requirements

Underfeeding diet (UF)

Intervention Type OTHER

Diet in which the calories are 50% of their weight maintaining energy requirements

Interventions

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Vancomycin

Vancomycin 125mg orally four times per day for 12 days

Intervention Type DRUG

Placebo oral tablet

Placebo pills orally four times per day for 12 days

Intervention Type DRUG

Overfeeding diet (OF)

Diet in which the calories are 150% of their weight maintaining energy requirements

Intervention Type OTHER

Underfeeding diet (UF)

Diet in which the calories are 50% of their weight maintaining energy requirements

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

Free of acute and chronic diseases (especially GI disorders) as determined by medical history, physical examination and laboratory tests.

Individuals may be taking laxative drugs but they must be discontinued 3 or more weeks before admission.

Age 18-45 y (in order to minimize the affect of aging on nutrient absorption).

Exclusion Criteria

Because it is unclear how chronic illnesses or substance abuse could affect nutrient absorption we will exclude volunteers with chronic diseases or current substance abuse. This is especially important because the limited number of study subjects in this study will make it hard to control for these confounders. We will therefore exclude subjects with a history or clinical manifestation of:

* Current smoking
* Type 2 diabetes (according to the World Health Organization diagnostic criteria)
* Endocrine disorders, such as Cushing s disease, pituitary disorders, and hypo- and hyperthyroidism
* HIV infection (self-report), due to effects on weight and body composition of HIV and medications used to treat HIV
* Active tuberculosis (self-report)
* Asthma on active daily treatment with medications
* Pulmonary disorders including physician diagnosed chronic obstructive pulmonary diseases and obstructive sleep apnea syndrome
* Cardiovascular diseases, including coronary heart disease, heart failure, arrhythmias, and peripheral artery disease
* Hypertension (according to the World Health Organization diagnostic criteria), treated or uncontrolled
* Gastrointestinal disease, including inflammatory bowel diseases (e.g. Crohn s disease and ulcerative colitis), malabsorption syndromes (e.g. celiac disease), gastric ulcer (active) and irritable bowel syndrome.
* Lactose intolerance
* Anemia (defined as hemoglobin \< 11 mg/dl), leucopenia (defined as white blood cell count \< 4,000/microL) or thrombocytopenia (defined as platelet count \< 150,000/microL)
* Liver disease, including non-alcoholic fatty liver disease or current elevated liver enzymes over 1.5 times the normal range for AST, ALT or GGT or a history and physical exam that indicates a potential liver disease as describe by Giannini et al
* Evidence of chronic renal disease as defined by estimated glomerular filtration rate of \< 60 ml/min or evidence of overt proteinuria on urine dipstick.
* Central nervous system disease, including previous history of cerebrovascular accidents, dementia, and neurodegenerative disorders
* Cancer requiring treatment in the past five years, except for non-melanoma skin cancers or cancers that have clearly been cured or in the opinion of the investigator carry an excellent prognosis
* Behavioral or psychiatric conditions that would be incompatible with a safe and successful participation in the study (such as major depression, schizophrenia and presence of psychotic symptoms)
* Eating disorders such as anorexia nervosa, bulimia or binge eating syndrome
* Taking weight loss drugs
* Weight change of more than 5% of total body weight in the 3 months before admission
* Use of any antibiotic or probiotic agents within 6 months prior to minimize the potential effects of these substances on the gut microbiota.
* Use of antacids (Proton pump inhibitors, H2 antagonists or aluminum/magnesium hydroxide) 3 months prior to the study assessed by self-report because a modified gastric pH might affect the gut microbiota as well
* Evidence of alcohol and/or drug abuse (more than 3 drinks per day and use of drugs, such as amphetamines, cocaine, heroin, or marijuana)

* Known allergies to vancomycin
* Known allergies to heparin or a history of heparin-induced thrombocytopenia
* Personal history or evidence of a bleeding disorder

All individuals will be fully informed of the aim, nature, and risks of the study prior to giving written informed consent. The study s informed consent will be obtained by a principal or associate investigator, research physician or physician assistant working in the clinical research unit.

Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No