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Updated: Aug 19, 2026

Murine Renal Transplantation Procedure
Published on: July 10, 2009
Intra-individual variation of cystatin C and creatinine in pediatric solid organ transplant recipients
Ludmila Podracka1, Janusz Feber, Nathalie Lepage
1Department of Pediatrics, Children's Hospital of Eastern Ontario, University of Ottawa, Ottawa, Ontario, Canada.
Insights
Cystatin C (CysC) and serum creatinine (SCr) show similar variability for monitoring kidney function in pediatric transplant patients. Both markers are useful for tracking changes in glomerular filtration rate (GFR) over time post-transplant.
Area of Science:
- Pediatric Nephrology
- Transplantation Medicine
- Biomarker Analysis
Background:
- Glomerular filtration rate (GFR) monitoring is crucial post-solid organ transplant (Tx).
- Controversy exists regarding the reliability of cystatin C (CysC) versus serum creatinine (SCr) for GFR assessment in transplant recipients.
- Pediatric transplant patients require accurate and consistent GFR evaluation.
Purpose of the Study:
- To compare the intra-patient variability of CysC and SCr in children following solid organ transplantation.
- To evaluate the feasibility of CysC as a GFR marker in this population.
- To assess GFR estimation formulas based on CysC against the established Schwartz formula.
Main Methods:
- Analysis of 178 simultaneous SCr and CysC measurements from 20 pediatric solid organ transplant recipients.
- Calculation of intra-individual coefficient of variation (CV) for SCr and CysC.
- Comparison of GFR estimated by the Schwartz formula and a CysC-based formula.
Main Results:
- Mean CV for SCr was 7.71% and for CysC was 10.27% (p=0.04), with no significant difference when excluding patients with bladder augmentation.
- CV for GFR estimated by the Schwartz formula (7.44%) was significantly lower than GFR calculated from CysC (12.52%, p=0.001).
- CysC and CysC-calculated GFR demonstrated equivalent, but not superior, performance compared to SCr and the Schwartz formula for longitudinal follow-up.
Conclusions:
- Cystatin C can be utilized for longitudinal, intra-individual monitoring of renal function in pediatric transplant recipients.
- Both cystatin C and serum creatinine are viable markers for assessing GFR changes post-transplant.
- Further studies with larger cohorts may clarify the role of CysC in specific transplant scenarios.
Abstract:
There is controversy about the feasibility of cystatin C (CysC) as a marker of glomerular filtration rate (GFR) post-transplant (Tx). We studied intra-patient variability of CysC in comparison with serum creatinine (SCr) in 20 children (11 males, mean age 11.5 +/- 6.4 yr) with solid organ transplants (14 kidney, four liver, and two combined liver + kidney transplants). The mean age at Tx was 7.0 +/- 5.6 yr. A total of 178 simultaneous SCr and CysC measurements (median 8 per patient) were analyzed. In addition, GFR was calculated using the Schwartz and a novel CysC-based formula. Intra-individual coefficient of variations (CV) was calculated as ratio of standard deviation over mean. The mean CV was significantly lower for SCr (7.71 +/- 4.16%) when compared with CysC (10.27 +/- 4.87, p = 0.04), but was no longer significantly different when excluding patients with a bladder augment. The CV of the GFR estimated by Schwartz formula (7.44 +/- 3.77) was significantly lower than GFR calculated from CysC (12.52 +/- 7.37), p = 0.001. The mean ratio between the Schwartz GFR and the GFR calculated from CysC was 102.6 +/- 12.8%, not significantly different from 100% (p = 0.3796). The only potential confounding factors to explain increased CV after Tx were gender and bladder augmentation, whereas calcineurin inhibitors or steroids did not influence CV. With the limitation of a small number of subjects, our data suggest that the CysC and the CysC-calculated GFR is equivalent but not better than SCr and Schwartz formula. We therefore conclude that measurement of CysC can be used for longitudinal intra-individual follow-up of renal function post-Tx.
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