Removal of Protein-Bound, Hydrophobic Uremic Toxins by a Combined Fractionated Plasma Separation and Adsorption Technique

Protein‐bound uremic toxins, such as phenylacetic acid, indoxyl sulfate, and p‐cresyl sulfate, contribute substantially to the progression of chronic kidney disease (CKD) and cardiovascular disease (CVD). However, based on their protein binding, these hydrophobic uremic toxins are poorly cleared dur...

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Published inArtificial organs Vol. 37; no. 4; pp. 409 - 416
Main Authors Brettschneider, Falko, Tölle, Markus, von der Giet, Markus, Passlick-Deetjen, Jutta, Steppan, Sonja, Peter, Mirjam, Jankowski, Vera, Krause, Alfred, Kühne, Sophie, Zidek, Walter, Jankowski, Joachim
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.04.2013
Wiley Subscription Services, Inc
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Summary:Protein‐bound uremic toxins, such as phenylacetic acid, indoxyl sulfate, and p‐cresyl sulfate, contribute substantially to the progression of chronic kidney disease (CKD) and cardiovascular disease (CVD). However, based on their protein binding, these hydrophobic uremic toxins are poorly cleared during conventional dialysis and thus accumulate in CKD‐5D patients. Therefore, we investigated whether hydrophobic and cationic adsorbers are more effective for removal of protein‐bound, hydrophobic uremic toxins than conventional high‐flux hemodialyzer. Five CKD‐5D patients were treated using the fractionated plasma separation, adsorption, and dialysis (FPAD) system for 5 h. A control group of five CKD patients was treated with conventional high‐flux hemodialysis. Plasma concentrations of phenylacetic acid, indoxyl sulfate, and p‐cresyl sulfate were measured. Removal rates of FPAD treatment in comparison to conventional high‐flux hemodialysis were increased by 130% for phenylacetic acid, 187% for indoxyl sulfate, and 127% for p‐cresol. FPAD treatment was tolerated well in terms of clinically relevant biochemical parameters. However, patients suffered from mild nausea 2 h after the start of the treatment, which persisted until the end of treatment. Due to the high impact of protein‐bound, hydrophobic uremic toxins on progression of CKD and CVD in CKD‐5D patients, the use of an adsorber in combination with dialysis membranes may be a new therapeutic option to increase the removal rate of these uremic toxins. However, larger, long‐term prospective clinical trials are needed to demonstrate the impact on clinical outcome.
Bibliography:istex:8B4CEF24F524C792C3E5DDF81457602763B4852F
Sonnenfeld Foundation
Federal Ministry of Economics and Technology - No. KF2263201 SB9
Federal Ministry of Education and Research - No. NGFN/01GR0807
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ArticleID:AOR1570
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ISSN:0160-564X
1525-1594
DOI:10.1111/j.1525-1594.2012.01570.x