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Completed

NCT Number: NCT04255368

Choline Source, Gut Microbiota and Trimethylamine-N-oxide Response

The purpose of this research is to determine the production of trimethylamine-N-oxide (TMAO) from different forms of choline and whether this response is modified by the gut microbiota composition.

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Key information

Conditions

Age range

21 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Center for Human Nutrition Studies Clinic, Utah State University

Logan, Utah, 84322, United States

About this study

The overall goal of this research is to identify dietary and physiological factors contributing to elevated levels of trimethylamine-N-oxide (TMAO), a choline-derived gut-microbiome-dependent metabolite that has been identified to increase cardiovascular disease risk. Our recent findings indicate that the gut microbiome may account for variations in TMAO levels, whereby those with a greater enrichment of Firmicutes to Bacteroidetes had elevated TMAO response to dietary precursor intake. However, the interaction between choline intake and gut microbiota composition as a determinant of interindividual variations in TMAO response has not been investigated. This study sought to i) compare plasma and urinary TMAO response after acute challenge containing different forms of choline; and ii) to determine the association between differences in TMAO response with differences in gut microbiota composition. To accomplish these objectives, a randomized, controlled cross-over study was conducted in healthy participants (n=41). The study incorporated three arms comprised of study meals containing (i) 600 mg choline as choline bitartrate; (ii) 600 mg choline as phosphatidylcholine; or (iii) no choline. Each meal was served with a bagel with margarine-butter spread and one cup of water, administered in a single day and separated by a 1-week washout period. Baseline blood sample was obtained by a phlebotomist using a standard venipuncture procedure, and participants collected their baseline urine sample. They also turned in a one-time self-collected baseline stool sample. Following the consumption of the study meal, serial blood samples were collected at 30 min and 1, 2, 4 and 6 h, and urine samples collected throughout the 6 h study period. At 4.5 h, participants were provided a fixed fruit snack (i.e., 2 single serving prepackaged applesauce) and water.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy men and women of any race or ethnicity
  • Age 21-50 y
  • BMI 20-24.9 kg/m2 or BMI 30-39.9 kg/m2

Exclusion criteria

  • Age > 50 y
  • BMI outside of the normal-weight or obese range (BMI < 20 kg/m2; BMI 25-29.9 kg/m2; or BMI > or = 40 kg/m2)
  • Pregnant or planning to become pregnant during the course of the study; currently breastfeeding (females)
  • Vegetarians
  • Smokers or recreational drug users
  • Individuals with gastrointestinal diseases or complaints, chronic illnesses or other metabolic diseases (including trimethylaminuria)
  • Individuals who have taken antibiotics within the past 2 months
  • Individuals who are not willing to discontinue pre- and probiotics and dietary supplements for the time leading up to 2 months before the study and during the study

Treatment and study plan

Water-soluble choline

Other

600 mg choline as choline bitartrate

Fat-soluble choline

Other

600 mg choline as phosphatidylcholine

No choline control

Other

No choline

Primary outcomes

  1. TMAO metabolite concentration change

    Time frame: Blood: study baseline, 30 minutes and 1 hour, 2 hours, 4 hours and 6 hours

    Plasma TMAO metabolite response

  2. TMAO metabolite concentration change

    Time frame: Urine: study baseline, pooled 6 hours study period

    Urinary TMAO metabolite response

  3. Gut microbiome profile

    Time frame: Stool: one-time baseline

    16S rRNA

Secondary outcomes

  1. One-carbon metabolite concentration change

    Time frame: Blood: study baseline, 30 minutes and 1 hour, 2 hours, 4 hours and 6 hours

    Plasma choline metabolite response

  2. Phosphatidylcholine concentration change

    Time frame: Blood: study baseline, 30 minutes and 1 hour, 2 hours, 4 hours and 6 hours

    Plasma phosphatidylcholine response

  3. One-carbon metabolite concentration change

    Time frame: Urine: study baseline, pooled 6 hours study period

    Urinary choline metabolite response

  4. Inflammation and cardiovascular disease risk marker concentration change

    Time frame: Blood: study baseline to 6 hours

    Plasma TNF-α and IL-6

  5. Flavin monooxygenase 3 (FMO3) 472 G>A genotype variant

    Time frame: Blood: study baseline

    Genetic polymorphism

Sponsors and collaborators

Lead sponsor

Utah State University

Other

Registry information

Official study title

Effect of Choline Source and Gut Microbiota Composition on Trimethylamine-N-oxide Response in Humans

Important dates

Study start
2017
Primary completion
2018
Study completion
2020
First posted
Feb 5, 2020
Registry last updated
Nov 4, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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