Leucine Requirement in Adult Men and Women
Study Details
Study Description
Brief Summary
The purpose of the study is to determine the body's nutritional need for the essential amino acid, leucine, in adult men and women 18 to 39 years of age.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
The experimental design will be based on the minimally invasive IAAO model (12). Each participant will be studied at a minimum of 4 and up to 7, randomly assigned, intake levels of leucine.
Subjects will be weighed at the pre-study assessment and at the start of each IAAO study day to ensure accurate prescription of diets and isotopes, and to confirm weight maintenance throughout the study.
Each study will consist of a 2-day adaptation period to a prescribed diet in accordance with the energy requirement of the subject and 1-study day. The diet will provide an adequate amount of protein, of 1 g protein∙kg-1∙d-1. The 2-day adaptation period is to allow the body to adapt to an adequate amount of protein as it has been shown that protein kinetics is altered without it. Following the 2 days of adaptation is the study day where leucine intake will be randomly assigned and phenylalanine (Phe) kinetics will be measured with the use of L-[1-13C]phenylalanine. On this day, VCO2 will be measured by calorimetry immediately after the 5th meal for a period of 20 minutes, and a 15ml blood sample will be collected at the end of each study visit to measure plasma amino acid levels, insulin, and glucose in males and females and progesterone, and estrogen in females.
For female participants, each level of intake will be studied both in the luteal and follicular phase of their menstrual cycle (up to 14 studies in total). For the follicular phase, the study will be conducted 3-7 days immediately after the 1st day of menstrual bleeding. For the luteal phase, the study will be conducted 4-7 days before the onset of next menstrual bleeding. The IAAO study day of the luteal phase will be set on the basis of each subject's length of their menstrual cycle, and the length and regularity of their cycle will be determined during the pre-study assessment.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Leucine intake For this study, each participant will be randomly assigned to receive up to 7 intake levels of leucine, ranging from 10 to 75 mg/kg/d. |
Dietary Supplement: Leucine
7 intake levels of leucine, ranging from 10 to 75 mg/kg/d.
|
Outcome Measures
Primary Outcome Measures
- F13CO2 [4.5 hours during study visits]
Rate of appearance of labelled carbon dioxide (13CO2) in breath from the oxidation of 13C-Phenylalanine
Secondary Outcome Measures
- 13C-phenylalanine enrichment [4.5 hours during study visits]
urinary 13C-phenylalanine enrichment
- Plasma amino acid concentrations [at end of each study visit]
To assess the effect of amino amino acid intake on plasma amino acid concentration.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Healthy adult males, 18 to 39 years of age.
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Healthy adult females, 18 to 39 years of age with regular menstrual cycles within in the last 12 months.
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Willingness to participate in the study and completed the screening procedures (height, weight, fasting blood sample and medical history questionnaire).
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No recent history of weight loss
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BMI between 18.5 - 27 kg/m 2
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Absence of chronic disease or acute illness that could affect protein and AA metabolism (diabetes, cancer, liver or kidney disease, HIV, acute cold or flu, COVID-19, hypo or hyperthyroidism, rheumatoid arthritis treated with anti-inflammatory medications).
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Non-smoking
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Willingness to consume the diet provided.
Exclusion Criteria:
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Presence of disease known to affect protein and AA metabolism (diabetes, cancer, liver or kidney disease, HIV, acute cold or flu, Covid-19, hypo or hyperthyroidism, rheumatoid arthritis treated with anti-inflammatory medications).
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On medications known to affect protein and amino acid metabolism (steroids) or taking oral contraceptive pills or other birth control devices that would affect sex hormone profiles over the last 2 years.
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Pregnant or lactating women.
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Recent significant weight loss; ≥ 5% of body with in the last 3 months.
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Individuals on weight reducing diets.
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Inability to tolerate the diet
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Unwilling to have blood drawn from a venous access, or using a ventilated hood indirect calorimeter for the purposes of the study.
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Significant coffee consumption of more than 2 cups/day
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Significant alcohol consumption of more than one drink/day
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Failure to disclose any of the information needed to assess eligibility.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | The Hospital for Sick Children | Toronto | Ontario | Canada | M5G 1X8 |
Sponsors and Collaborators
- The Hospital for Sick Children
- Canadian Institutes of Health Research (CIHR)
Investigators
- Principal Investigator: Glenda Courtney-Martin, PhD, RD, The Hospital for Sick Children
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 1000078896