Determination of Threonine Requirements in Healthy School-aged Children

Threonine Requirements in Children Clinical Trial

Official title:

Determination of Threonine Requirements and the Metabolic Availability of Threonine From Food Sources in Healthy School-aged Children

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02660892
• Other study ID #: H15-02691
• Status: Completed
• Phase: N/A
• Start date: May 26, 2016
• Est. completion date: October 1, 2017

Study information

• Verified date: February 2020
• Source: University of British Columbia
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Threonine is an indispensable amino acid (nutrient containing nitrogen), which cannot be made in the body and must be consumed from food. Amino acids are the building blocks of protein in your body, and need to be eaten in required amounts to maintain health and growth. Deficiency in threonine can affect small intestine growth due to its structural importance in the intestinal protein mucin. While threonine is found in many foods, deficiency can occur in developing countries where nutrition is primarily plant based, and low in available protein.

Therefore, the purpose of this study is to determine the requirement of the indispensable amino acid Threonine, in school-aged children (6-10y). Secondly, we wish to determine the availability of threonine from three test proteins (soy, green pea, casein).

Description:

The threonine intake requirement for children are based on factorial calculations. In the current study we will use a new and modern technique, the indicator amino acid oxidation technique (IAAO), to determine threonine requirements in children.

This technique is a newer technique which involves the consumption of protein shakes composed of specific amounts of threonine mixed with a stable isotope tracer. The oxidation of this isotope will be measured in urine and breath to determine a breakpoint (requirement) of threonine.

Determining the requirement for threonine, as well as the availability of threonine from various food products will help us to develop better food recommendations for children.

Research Method This study will be carried out in a repeated measures design. Participants will be recruited and screened for eligibility. Six participants will be brought in for 6 testing visits with reference amino acid, where they will be randomized to a level of threonine intake. A further 3 visits will be carried out during which participants will be randomized to a level of threonine consumption derived from alternative proteins (casein, soy, peas) which is at a threshold below the requirement for threonine to determine availability.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 6
• Est. completion date: October 1, 2017
• Est. primary completion date: July 5, 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 6 Years to 10 Years

Eligibility

Inclusion Criteria:

• Children between 6 and 10 Y

• No history of chronic disease or metabolic disorders

• No food allergies

• No recent illness or antibiotic consumption

• Children with a normal, healthy, body weight (between 3rd and 85th percentiles for their age group for weight) (Dietitians of Canada, 2015)

Exclusion Criteria:

• Children under 6 years' old

• Children over 10 years' old

• Children with a history of disease or metabolic disorders

• Children with any food allergies

• Children taking prescription medication

• Children with a history of being underweight, overweight, or obese (Dietitians of Canada, 2015; Onis et al., 2007)

o Below 3rd percentile for weight, Above 85th percentile for weight

• Female children who have commenced menstruation

Related Conditions & MeSH terms

• Threonine Requirements in Children

Intervention

Dietary Supplement:
• Protein intake
Oral consumption of eight hourly experimental meals 4 tracer free experimental meals containing a mixture of free amino acids and calories from protein free flavoured liquid, protein free cookies and corn oil 4 isotopically labeled experimental meals.

Locations

Country	Name	City	State
Canada	BC Children's Hospital Research Institute	Vancouver	British Columbia

Sponsors (1)

Lead Sponsor	Collaborator
University of British Columbia

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	13 Co2 production	Urine and breath samples will be collected during the study day, to measure the rate of oxidation of tracer phenylalanine in the expired breath, and flux enrichment in urine.	8 hours (1 study day)