Malnutrition, including muscle wasting commonly occurs in children with cystic fibrosis (CF), negatively influencing their quality of life and survival. At the time of a diagnosis of CF, severe protein deficits can already be present. It is important to get CF children fed adequately to prevent that their condition becomes worse or that recovery takes longer. Oral supplementation trials showed that gains in lean body mass are difficult to achieve in CF unless specific metabolic abnormalities are targeted. However, the specific needs for certain food components are not clear yet in children that are ill. Therefore, more information is necessary on the need for protein and certain amino acids in children with CF. Previous studies support the concept of essential amino acids (EAA) as an anabolic stimulus in the young and elderly and in insulin resistant states. Until yet no information is present on the anabolic effects of EAA in CF. It is therefore our hypothesis that a high-leucine essential amino acids mixture specifically designed to stimulate protein anabolism will target the metabolic alterations of pediatric subjects with CF. In the present proposal, the acute metabolic effects of this high leucine essential amino acids mixture will be examined in pediatric subjects with CF and compared to that of a regular balanced total mixture of essential and non-essential amino acids. The principal endpoints will be the extent of stimulation of whole body protein synthesis as this is the principal mechanism by which either amino acid or protein intake causes muscle anabolism, and the reduction in endogenous protein breakdown. Both endpoints will be assessed by isotope methodology which is thought to be the reference method.
In this study, we will test the following hypothesis: A high-leucine essential amino acid mixture (dose of 6.7 g) will stimulate protein anabolism to a greater extent than a standard balanced mixture of total (essential and non-essential) amino acids in CF pediatric subjects. The principal endpoints will be the extent of stimulation of protein synthesis rate and the reduction in endogenous protein breakdown. The current project will provide information that will enable us to better understand the underlying metabolic mechanisms that regulate protein metabolism in pediatric subjects with CF.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
DOUBLE
Enrollment
14
7 g as bolus
University of Arkansas for Medical Sciences
Little Rock, Arkansas, United States
Net whole body protein synthesis rate
Acute change from postabsorptive state after intake of essential amino acid + LEU vs total amino acid supplement
Time frame: Up to 2 years
Whole body collagen breakdown rate
Acute change from postabsorptive state after intake of essential amino acid + LEU vs total amino acid supplement
Time frame: Up to 2 years
Urea turnover rate
Acute change from postabsorptive state after intake of essential amino acid + LEU vs total amino acid supplement
Time frame: Up to 2 years
Arginine turnover rate
Measured in postabsorptive state
Time frame: Up to 2 years
Liver protein synthesis rate
Acute change from postabsorptive state after intake of essential amino acid + LEU vs total amino acid supplement
Time frame: Up to 2 years
Resting Energy expenditure
Measured in postabsorptive state
Time frame: Up to 2 years
Insulin kinetics
Acute change from postabsorptive state after intake of essential amino acid + LEU vs total amino acid supplement
Time frame: Up to 2 years
Amino acid kinetics
Acute change from postabsorptive state after intake of essential amino acid + LEU vs total amino acid supplement
Time frame: Up to 2 years
Glucose kinetics
Acute change from postabsorptive state after intake of essential amino acid + LEU vs total amino acid supplement
Time frame: Up to 2 years
Fat-free mass
Characterization of subjects
Time frame: Up to 2 years
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