The Impact of Dialysis Modality on Serum Heat Shock Proteins in Children and Young Adults with Chronic Kidney Disease

Background/Aims: The acceleration of atherosclerosis by dialysis is not completely understood. The elevated levels of heat shock proteins (HSP) and antibodies against them were described in adults with atherosclerotic lesions, but there are no investigations on them in dialyzed patients. The aim of...

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Published inKidney & blood pressure research Vol. 32; no. 5; pp. 366 - 372
Main Authors Musiał, Kinga, Szczepańska, Maria, Szprynger, Krystyna, Zwolińska, Danuta
Format Journal Article
LanguageEnglish
Published Basel, Switzerland S. Karger AG 01.01.2009
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Summary:Background/Aims: The acceleration of atherosclerosis by dialysis is not completely understood. The elevated levels of heat shock proteins (HSP) and antibodies against them were described in adults with atherosclerotic lesions, but there are no investigations on them in dialyzed patients. The aim of the studywas to evaluate the serum HSP, their connections with dialysis modality and their possible role as markers of atherosclerosis. Methods: Hsp60, Hsp90-α, anti-Hsp60 and anti-Hsp70 concentrations were assessed by ELISA in 19 children on automated peritoneal dialysis (APD) and 17 patients on hemodialysis (HD). hsCRP, sE-selectin, IL-4, IL-12 and the lipid profile were also estimated. Results: Hsp60 values were lower, whereas Hsp90-α was higher in the dialyzed children than in the controls, without any difference between the dialysis modalities. The anti-Hsp60 concentrations were increased in all patients and higher in HD patients than in APD patients. The anti-Hsp70 levels in the APD children were decreased versus controls. Anti-Hsp60 correlated with HDL-cholesterol in APD children, and with total cholesterol and LDL-cholesterol in HD patients. Anti-Hsp70 correlated with sE-selectin in HD subjects. Conclusions: The levels of antibodies against HSP seem to distinguish between the dialysis modalities and the correlations with the lipid profile and sE-selectin, suggesting their potential role as markers of atherosclerosis.
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ISSN:1420-4096
1423-0143
1423-0143
DOI:10.1159/000254336