Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (13)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Kooman, J.
Right arrow Articles by Leunissen, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kooman, J.
Right arrow Articles by Leunissen, K.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nephrology Dialysis Transplantation, Vol 12, Issue 11 2397-2401, Copyright © 1997 by Oxford University Press


PRELIMINARY REPORTS

The influence of bicarbonate supplementation on plasma levels of branched-chain amino acids in haemodialysis patients with metabolic acidosis

J Kooman, N Deutz, P Zijlmans, A an den Wall Bake, P Gerlag, F van Hooff and K Leunissen
Department of Internal Medicine, University Hospital Maastricht, The Netherlands; Department of Surgery, University of Limburg, Maastricht, The Netherlands; St Joseph Hospital Veldhoven, The Netherlands; Corresponding author at: Department of Internal Medicine, PO Box 5800, 6202 AZ Maastricht, The Netherlands

Background: It has been hypothesized that correction of metabolic acidosis might improve the nutritional state of acidotic haemodialysis (HD) patients partly because of a reduced oxidation of branched-chain amino acids (BCAA). Aim: We investigated whether bicarbonate (Bic) supplementation in acidotic HD patients results in increased plasma levels of BCAA. Methods: In a longitudinal study (run-in period, 2 months; study period, 6 months), the effect of Bic supplementation on plasma levels of BCAA was studied in 12 acidotic HD patients (7 men, 5 women, mean age 54±18 years) with a predialysis bicarbonate (Bic) concentration smaller or equal to 22 mmol/l. Bic was supplemented by increasing Bic concentration of the dialysate and by oral Bic supplementation. Results: Predialysis Bic increased significantly during the study period (18.7±2.7 vs 23.1±11.5 mmol/l). There was no change in nutritional parameters. However, plasma levels of the BCAA valine, leucine, and isoleucine increased significantly. Conclusions: In haemodialysis patients with metabolic acidosis, Bic supplementation over a 6-months period resulted in an increase in plasma levels of BCAA. Further study is needed to elucidate the mechanisms behind, and the clinical importance of the observed changes in plasma BCAA levels.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
J. Am. Soc. Nephrol.Home page
I. de Brito-Ashurst, M. Varagunam, M. J. Raftery, and M. M. Yaqoob
Bicarbonate Supplementation Slows Progression of CKD and Improves Nutritional Status
J. Am. Soc. Nephrol., September 1, 2009; 20(9): 2075 - 2084.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
C. P. Kovesdy, J. E. Anderson, and K. Kalantar-Zadeh
Association of serum bicarbonate levels with mortality in patients with non-dialysis-dependent CKD
Nephrol. Dial. Transplant., April 1, 2009; 24(4): 1232 - 1237.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
N. J. M. Cano, D. Fouque, and X. M. Leverve
Application of Branched-Chain Amino Acids in Human Pathological States: Renal Failure
J. Nutr., January 1, 2006; 136(1): 299S - 307S.
[Abstract] [Full Text] [PDF]


Home page
Nephrol Dial TransplantHome page
F. Locatelli, A. Covic, C. Chazot, K. Leunissen, J. Luno, and M. Yaqoob
Optimal composition of the dialysate, with emphasis on its influence on blood pressure
Nephrol. Dial. Transplant., April 1, 2004; 19(4): 785 - 796.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.