Oral Protein Supplementation Alone Improves Anabolism in a Dose-Dependent Manner in Chronic Hemodialysis Patients
Objective
We examined the protein anabolic effects of Pro-Stat 64, a high nitrogen-containing, enzyme-hydrolyzed, tryptophan-fortified, collagen protein supplement administrated during hemodialysis, at two different dosing regimens.
Design
This was a randomized, controlled, prospective study with 3 different groups: control, single dose of supplementation, and double dose of supplementation.
Setting
This study was performed at a clinical research center.
Patients
Six prevalent chronic hemodialysis (HD) patients were enrolled: 5 males, 1 female, 4 African Americans, and 2 Caucasians. Their mean age was 45 ± 11 years (S.D.). Two patients were diabetic.
Methods
Protein turnover studies were performed using amino-acid (AA) balance and primed constant infusion of L-(1-13C) leucine.
Main Outcome Measure
Whole-body protein balance was determined according to substrate kinetics.
Results
There were no statistically significant difference at any time point between protocols for blood chemistries and hormonal markers, except for minor variations in plasma glucose. All plasma AA groups displayed decreases during a control study, in which no supplementation was given. Compared with the control group, plasma nonessential AA and total AA concentrations were statistically significantly higher during HD after both single and double doses of supplementation. The forearm arteriovenous AA balance was statistically significantly better for essential, nonessential, and total AA uptake after both single-dose and double-dose supplementation compared with the control group, except for nonessential AA, which was significantly better only after a double dose. Whole-body protein breakdown and net protein balance were statistically significantly better during HD with a double-dose administration in a dose-dependent manner, compared with the control and single-dose groups.
Conclusions
Oral AA supplementation alone improves whole-body and skeletal muscle protein anabolism in a dose-dependent manner in chronic HD patients. These data should be taken into account during clinical decision-making or when designing clinical trials of nutritional supplementation.
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This study was supported in part by National Institutes of Health grants R01-DK45604 and K24-DK62849, by Diabetes Research Training Center Grant DK-20593 from the National Institute of Diabetes, Digestive and Kidney Diseases, by grant UL1 RR024975 from the National Center for Research Resources, and by an unrestricted grant from Medical Nutrition USA, Inc. M.B.S. is supported in part by a grant from the National Kidney Foundation Council of Renal Nutrition. K.L.C. is supported by grant K23 K23-DK080952 from the National Institute of Diabetes, Digestive and Kidney Diseases.
The authors declare no conflict of interest with regard to involvement with the commercial entities that supplied nutritional supplements.
PII: S1051-2276(09)00041-7
doi:10.1053/j.jrn.2009.01.019
© 2009 National Kidney Foundation, Inc. Published by Elsevier Inc All rights reserved.

