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Published on: September 1, 2015
Cystatin C levels in functionally anephric patients undergoing dialysis: the effect of different methods and
Najila Al-Malki1, Paul A Heidenheim, Guido Filler
1Department of Medicine, and London Health Sciences Centre, Nephrology Division, The University of Western Ontario, London, Canada.
Insights
Serum cystatin C levels are influenced by dialysis method and intensity. This protein may help monitor dialysis adequacy in patients with kidney failure.
Area of Science:
- Nephrology
- Biochemistry
- Clinical Chemistry
Background:
- Cystatin C is a protein filtered by glomeruli and degraded by tubules.
- Serum cystatin C concentration is a proposed marker for glomerular filtration rate (GFR).
- Cystatin C's molecular size suggests it is dialyzable.
Purpose of the Study:
- To investigate the influence of dialysis method and intensity on serum cystatin C levels.
- To assess cystatin C as a potential marker for dialysis adequacy.
Main Methods:
- Cross-sectional pilot study of functionally anephric dialysis patients.
- Measured predialysis cystatin C in patients undergoing conventional, nocturnal, daily hemodialysis, and automated peritoneal dialysis.
- Assessed urea kinetic parameters (Sp Kt/V, Std Kt/V, nPNA) and inflammatory markers (CRP, TSH).
Main Results:
- Serum cystatin C levels showed significant differences across dialysis modalities.
- A significant inverse linear correlation was found between cystatin C and standard weekly Kt/V (Std Kt/V).
- Cystatin C levels were stable and not influenced by nPNA, CRP, or TSH.
Conclusions:
- Dialysis method and intensity significantly influence serum cystatin C levels.
- Serum cystatin C may serve as a valuable tool for monitoring dialysis treatment adequacy.
Background And Objectives:
Cystatin C, a low molecular weight protein, is produced by nucleated cells, filtered by glomeruli, and degraded by tubules at a constant rate. Its serum concentration has been proposed as a marker of GFR. Its size should make it dialyzable. It is hypothesized that serum cystatin C levels are influenced by the method and intensity of dialysis received.
Design:
This is a cross-sectional pilot study of cystatin C in functionally anephric dialysis patients. It was measured predialysis in 14 patients on conventional (3 to 5 h, 3 x wk) hemodialysis; eight on nocturnal hemodialysis (three to seven nights, 6 to 8 h); three on daily hemodialysis (6 d, 1(1/2) to 2(1/2) h); and 10 on automated peritoneal dialysis. All had urea kinetic studies and values for single pool Kt/V (Sp Kt/V), standard weekly Kt/V (Std Kt/V), and protein equivalent of nitrogen appearance (nPNA; g/kg/d). C reactive protein (CRP; mg/L) and thyroid stimulating hormone (TSH; mIU/L) were measured as factors known to influence cystatin C.
Results:
There was no correlation between cystatin C and Sp Kt/V, but there was a significant inverse linear correlation with Std Kt/V and there were significant differences between treatment modalities in cystatin C levels and in Std Kt/V. The estimation of cystatin C was reliable and stable over 3 to 6 wk and its levels uninfluenced by nPNA, CRP, or TSH.
Conclusion:
Serum cystatin C levels are influenced by the method and intensity of dialysis and may have a role in treatment adequacy monitoring.
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