Effects of Amino Acid Supplementation on Liver Lipid Content and Protein Metabolism in Obese Children

Sponsor
Arkansas Children's Hospital Research Institute (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT02337894
Collaborator
(none)
32
2
12.1

Study Details

Study Description

Brief Summary

The purpose of this study is to assess the effect of an eight-week dietary supplementation with essential amino acids plus arginine on liver and plasma lipid content, whole-body fat oxidation, whole-body insulin sensitivity, whole body protein metabolism, and body composition in obese pre-pubertal children.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Essential amino acids plus arginine
  • Dietary Supplement: Placebo
N/A

Detailed Description

Up to thirty-two obese pre-pubertal children will be recruited for this study. Up to sixteen will be boys and up to sixteen will be girls. The study will be a double-blinded, placebo-controlled trial using a randomized, but counter-balanced design. This will ensure equal numbers in the two groups that the children are randomized to, for each sex. The control group will receive placebo and the intervention group will receive essential amino acids plus arginine. The supplements (essential amino acids plus arginine, and placebo) will be given in the form of a drink twice a day for a total of 8 weeks. Both the participants and the investigators will be blinded to group assignment.

The primary endpoints of this study are to assess the effect of essential amino acids (EAA) plus arginine supplementation on lipid and protein metabolism. For this, liver lipid content, hepatic apoptosis, plasma lipids, apolipoprotein B-100 (apo B-100) levels, hepatic fatty oxidation, whole body insulin sensitivity, body composition and whole body protein turnover. will be compared between the intervention and placebo groups.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
32 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Other
Official Title:
Effects of Nutritional Supplementation With Amino Acids on Liver Lipid Content, Whole-body Protein Turnover, and Body Composition in Obese Pre-pubertal Children
Anticipated Study Start Date :
Jan 30, 2022
Anticipated Primary Completion Date :
Feb 1, 2023
Anticipated Study Completion Date :
Feb 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Essential amino acids plus arginine

Children randomized to the intervention group will receive a supplement containing essential amino acids plus arginine in the form of a drink which they will have to take for 8 weeks. Measurement of liver lipid content, hepatic apoptosis, plasma lipids, apolipoprotein B-100 levels, hepatic fatty oxidation, whole body insulin sensitivity, body composition and whole body protein turnover will be compared with the the placebo group, and before and after the intervention.

Dietary Supplement: Essential amino acids plus arginine
Flavored drink containing essential amino acids plus arginine.

Placebo Comparator: Control drink

The control drinks will be indistinguishable from the intervention drinks in taste and volume, but will contain placebo rather than essential amino acids plus arginine.

Dietary Supplement: Placebo
Flavored drink without essential amino acids plus arginine.

Outcome Measures

Primary Outcome Measures

  1. Serum levels of markers of lipid metabolism before and after 8 weeks of supplementation with essential amino acids plus arginine vs placebo. [Baseline and 8 weeks]

    Change in serum levels of triglycerides, cholesterol, very low density lipoprotein (VLDL), low density lipoprotein (LDL), beta-hydroxybutyrate, Apo-lipoprotein B and plasma cytokeratin 18 will be assessed after 8 weeks of essential amino acids plus arginine vs placebo.

  2. Liver lipid content before and after 8 weeks of supplementation with essential amino acids plus arginine vs placebo. [Baseline and 8 weeks]

    Nuclear Magnetic Resonance Spectroscopy will be used to assess changes in liver lipid content following an 8-week supplementation period with essential amino acids plus arginine vs. placebo.

  3. Whole body protein turnover before and after 8 weeks of supplementation with essential amino acids plus arginine vs. placebo. [Baseline and 8 weeks]

    Change in whole body protein metabolism (synthesis and breakdown) following 8 weeks of essential amino acids plus arginine vs placebo. This outcome will be assessed using a stable isotope of an amino acid (15N-alanine).

  4. Body composition before and after 8 weeks of supplementation with essential amino acids plus arginine vs. placebo. [Baseline and 8 weeks]

    Changes in body composition (fat free mass and fat mass) will be assessed using Dual-Energy X-ray Absorptiometry. Measurements will be carried out at baseline and following 8 weeks of supplementation with essential amino acids plus arginine vs. placebo.

Secondary Outcome Measures

  1. HOMA-IR index before and after 8 weeks of supplementation with essential amino acids plus arginine vs placebo. [Baseline and 8 weeks]

    Fasting glucose and insulin levels will be used to assess changes in the HOMA-IR index after 8 weeks of supplementation with essential amino acids plus arginine vs. placebo.

Eligibility Criteria

Criteria

Ages Eligible for Study:
7 Years to 10 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Healthy boy or girl

  • Age 7-10 years of age and Tanner stage no greater than stage 1

  • BMI ≥ 95th percentile

  • Not participating for more than 1 hour/week in a regular physical activity program

Exclusion Criteria:
  • Tanner stage greater than stage 1

  • Having known chronic illnesses/disorders that may independently affect study outcome measures: type 2 or type 1 diabetes mellitus, neurologic (e.g. epilepsy), neurobehavioral (e.g. Attention deficit disorder and hyperactivity, ADHD) endocrine, hepatic, autoimmune, cardiac and renal disorders. Also, chronic lung disorders except well controlled asthma that does not require permanent use of inhaled/oral steroids

  • Taking permanent medications: thyroid hormone replacement therapy, inhaled/oral steroids, insulin, metformin, anabolic drugs (growth hormone replacement therapy and oxandrolone) anti-lipid medication, blood pressure medication, ADHD medication (methylphenidate, amphetamines, atomoxetine)

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Arkansas Children's Hospital Research Institute

Investigators

  • Principal Investigator: Eva C Diaz, MD, University of Arkansas
  • Study Director: Elisabet Borsheim, Ph.D, University of Arkansas

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Arkansas Children's Hospital Research Institute
ClinicalTrials.gov Identifier:
NCT02337894
Other Study ID Numbers:
  • 203454
First Posted:
Jan 14, 2015
Last Update Posted:
Jan 13, 2021
Last Verified:
Jan 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Arkansas Children's Hospital Research Institute
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 13, 2021