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Prominent Accumulation in Hemodialysis Patients of Solutes Normally Cleared by Tubular Secretion

Overview
Specialty Nephrology
Date 2013 Nov 16
PMID 24231664
Citations 68
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Abstract

Dialytic clearance of urea is efficient, but other small solutes normally secreted by the kidney may be cleared less efficiently. This study tested whether the high concentrations of these solutes in hemodialysis patients reflect a failure of passive diffusion methods to duplicate the efficacy of clearance by tubular secretion. We compared the plasma concentrations and clearance rates of four solutes normally cleared by tubular secretion with the plasma concentrations and clearance rates of urea and creatinine in patients receiving maintenance hemodialysis and normal subjects. The predialysis concentrations (relative to normal subjects) of unbound phenylacetylglutamine (122-fold), hippurate (108-fold), indoxyl sulfate (116-fold), and p-cresol sulfate (41-fold) were much greater than the concentrations of urea (5-fold) and creatinine (13-fold). The dialytic clearance rates (relative to normal subjects) of unbound phenylacetylglutamine (0.37-fold), hippurate (0.16-fold), indoxyl sulfate (0.21-fold), and p-cresol sulfate (0.39-fold) were much lower than the rates of urea (4.2-fold) and creatinine (1.3-fold). Mathematical modeling showed that prominent accumulation of the normally secreted solutes in hemodialysis patients could be accounted for by lower dialytic clearance relative to physiologic clearance combined with the intermittency of treatment. Whether or not more efficient removal of normally secreted solutes improves outcomes in dialysis patients remains to be tested.

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References
1.
Meijers B, de Loor H, Bammens B, Verbeke K, Vanrenterghem Y, Evenepoel P . p-Cresyl sulfate and indoxyl sulfate in hemodialysis patients. Clin J Am Soc Nephrol. 2009; 4(12):1932-8. PMC: 2798868. DOI: 10.2215/CJN.02940509. View

2.
Burckhardt G . Drug transport by Organic Anion Transporters (OATs). Pharmacol Ther. 2012; 136(1):106-30. DOI: 10.1016/j.pharmthera.2012.07.010. View

3.
Vanholder R, Meert N, Van Biesen W, Meyer T, Hostetter T, Dhondt A . Why do patients on peritoneal dialysis have low blood levels of protein-bound solutes?. Nat Clin Pract Nephrol. 2008; 5(3):130-1. DOI: 10.1038/ncpneph1023. View

4.
Eloot S, Torremans A, De Smet R, Marescau B, De Deyn P, Verdonck P . Complex compartmental behavior of small water-soluble uremic retention solutes: evaluation by direct measurements in plasma and erythrocytes. Am J Kidney Dis. 2007; 50(2):279-88. DOI: 10.1053/j.ajkd.2007.05.009. View

5.
Meyer T, Leeper E, Bartlett D, Depner T, Lit Y, Robertson C . Increasing dialysate flow and dialyzer mass transfer area coefficient to increase the clearance of protein-bound solutes. J Am Soc Nephrol. 2004; 15(7):1927-35. DOI: 10.1097/01.asn.0000131521.62256.f0. View