Choline Uptake Study

Not Applicable

Completed

• Conditions: Choline Uptake; Kinetics
• Interventions: Dietary Supplement: Choline added as a salt; Dietary Supplement: Choline added as a phospholipid

• Registration Number: NCT03822169
• Lead Sponsor: Wageningen University and Research

Brief Summary

The study is a randomised, cross-over, double blind, controlled trial in which study participants will visit the research facility on two occasions under fasting conditions with a washout period of one week. During each visit, study subjects will receive a test shake with phospholipid-bound choline or a control shake with choline added as a salt and DHA added separately. The two shakes will be given in randomised order and blood will be collected via a catheter before and up-to 6 hours after choline consumption. All study participants will receive a standardised evening meal prior to each study day and asked not to drink alcohol or perform heavy exercise the day before each study day. Study subjects are also asked to avoid choline rich products the day before each test day. Study participants are offered a meal after the test day.

Detailed Description

Choline is water-soluble vitamin-like essential nutrient. It is made in small amounts by the liver, but humans need to receive choline through the diet or by supplementation for proper health. Pregnancy and lactation are times when demand for choline is especially high. Infant formula not made from cow's milk is therefore supplemented with choline. Choline is therefore widely used. It is normally added to food products as a salt. However, if choline is present in a natural form, bound to phospholipids, it may be more efficiently absorbed. Docosahexaenoic acids (DHA) are also bound to these phospholipids.

The primary objective is determine choline uptake and bioavailability after consumption of a test shake with phospholipid-bound choline (and DHA), and to compare this to a control shake with choline added as a salt (and DHA added as an oil). Secondary objective is to compare the uptake and bioavailability of DHA after the two shakes.

The study is a cross-over, double blind, controlled trial in which study participants will visit the research facility on two occasions under fasting conditions. Subjects will receive two different choline products in randomized order with a washout period of one week. Blood will be collected via a catheter before and up-to 6 hours after choline consumption.

Study Timeline

• Study First Submitted: 2019-01-25
• Study First Submitted QC: 2019-01-25
• Study First Posted: 2019-01-30
• Study Start: 2019-02-05
• Primary Completion: 2019-02-19
• Study Completion: 2019-02-19
• Status Verified: 2019-04
• Last Update Submitted: 2019-04-11
• Last Update Posted: 2019-04-12

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 18

Inclusion Criteria

• Apparently healthy men and women
• Age between 30 and 70 years
• Body mass index (BMI) between 18.5 and 24.9 kg/m2
• Having veins suitable for blood sampling via a catheter (judged by study nurse/ medical doctor)

Exclusion Criteria

• Any metabolic, gastrointestinal, inflammatory or chronic disease (such as diabetes, anaemia, hepatitis, cardiovascular disease)
• History of gastro-intestinal surgery or having (serious) gastro-intestinal complaints
• History of liver dysfunction (cirrhosis, hepatitis) or liver surgery
• Kidney dysfunction (self-reported)
• Use of medication that may influence the study results,
• such as laxatives, stomach protectors and drugs that can affect intestinal motility.
• Use of choline or fish oil supplements
• Reported slimming, medically prescribed or vegan diet
• Current smokers
• Alcohol intake ≥4 glasses of alcoholic beverages per day
• Pregnant, lactating or wishing to become pregnant in the period of the study (self-reported)
• Abuse of illicit drugs
• Food allergies for products that we use in the study
• Participation in another clinical trial at the same time
• Being an employee of the department Consumer Science & Health group of Wageningen Food & Biobased Research and/or Human Nutrition and Health

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Choline added as a salt	Choline added as a salt	control shake with choline added as a salt and added DHA.
Choline added as a phospholipid	Choline added as a phospholipid	A shake with phospholipid-bound choline (and bound DHA),

Primary Outcome Measures

Name	Time	Method
change in plasma betaine concentration	blood samples will be taken before and up to 6 hours after shake consumption	postprandial test, determine betaine in blood samples collected before and after a shake
change in plasma choline concentration	blood samples will be taken before and up to 6 hours after shake consumption	postprandial test, determine choline in blood samples collected before and after a shake
change in plasma dimethylglycine concentration	blood samples will be taken before and up to 6 hours after shake consumption	postprandial test, determine dimethylglycine in blood samples collected before and after a shake

Secondary Outcome Measures

Name	Time	Method
Change in plasma DHA concentration	blood samples will be taken before and up to 6 hours after shake consumption	postprandial test, determine DHA in blood samples collected before and after a shake

Trial Locations

Locations (1)

Stichting Wageningen Research; 🇳🇱 Wageningen, Gelderland, Netherlands