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.

Pediatric Transplantation
|January 26, 2005
PubMed

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.

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