Skip Navigation

NDT Plus 2008 1(Supplement 4):iv41-iv45; doi:10.1093/ndtplus/sfn123
This Article
Right arrow Full Text Freely available
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 Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Coester, A. M.
Right arrow Articles by Krediet, R. T.
Right arrow Search for Related Content
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author [2008]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org

This article appears in the following NDT Plus issue: Dialysis Initiatives May 2007, Berlin, Germany [View the issue table of contents]

The relationship between effluent potassium due to cellular release, free water transport and CA125 in peritoneal dialysis patients

Annemieke M. Coester1, Machteld M. Zweers1, Dirk R. de Waart2 and Raymond T. Krediet1

1 Division of Nephrology, Department of Medicine
2 Department of Experimental Hepatology, Academic Medical Centre, University of Amsterdam, The Netherlands

Correspondence: Annemieke M. Coester, Division of Nephrology, A01-114, Academic Medical Centre, University of Amsterdam, PO Box 22700, 1100 ED Amsterdam, The Netherlands. Tel: +31-20-5666137; Fax: +31-20-5668895; E-mail: a.m.coester{at}amc.uva.nl


   Abstract

Background. Recently, we found evidence of effluent potassium (K+) additional to diffusion and convection, suggesting cellular release (CR). Its relationship with free water transport (FWT) in stable peritoneal dialysis (PD) patients suggested an effect of hypertonicity of the dialysis solution leading to cell shrinkage. The aim of the present study was to reproduce these findings in groups according to PD duration and to further investigate the role of mesothelial cells in the observed phenomenon.

Methods. Standard peritoneal permeability analyses done with 3.86% glucose were analysed cross-sectionally in three different groups: short-term (n = 53) 0–2 years PD treatment; medium-term (n = 24) 2–4 years PD and long-term (n = 26) > 4 years PD.

Results. The time courses for FWT and cellular release of K+ (CR-K+) during the dwell were not significantly different among the groups. Cancer antigen (CA) 125 was highest in the short-term group (P ≤ 0.02) and had a strong positive correlation with mass transfer area coefficient of creatinine (MTAC-creatinine) only in the short-term group (r = 0.62, P ≤ 0.01). CA125 had no relationship with either CR-K+ or FWT, except for negative relationships in the short-term group (CR-K+, r = –0.41, P ≤ 0.05; FWT, r = –0.54, P ≤ 0.05).

Conclusion. We conclude that the correlation of CA125 and MTAC-creatinine is dependent on PD duration and underlines the in vitro observation that mesothelial cells produce vasoactive substances that may increase the peritoneal surface area. However, CA125 is not directly related to CR-K+ or FWT. Therefore, the relationship between FWT and CR-K+ is likely to reflect hypertonic cell shrinkage, regardless of the duration of PD, and confirms our earlier findings.

Received for publication February 19, 2008. Accepted for publication June 19, 2008.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




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.