Urinary calprotectin and posttransplant renal allograft injury

PLoS One. 2014 Nov 17;9(11):e113006. doi: 10.1371/journal.pone.0113006. eCollection 2014.

Abstract

Objective: Current methods do not predict the acute renal allograft injury immediately after kidney transplantation. We evaluated the diagnostic performance of urinary calprotectin for predicting immediate posttransplant allograft injury.

Methods: In a multicenter, prospective-cohort study of 144 incipient renal transplant recipients, we postoperatively measured urinary calprotectin using an enzyme-linked immunosorbent assay and estimated glomerular filtration rate (eGFR) after 4 weeks, 6 months, and 12 months.

Results: We observed a significant inverse association of urinary calprotectin concentrations and eGFR 4 weeks after transplantation (Spearman r = -0.33; P<0.001). Compared to the lowest quartile, patients in the highest quartile of urinary calprotectin had an increased risk for an eGFR less than 30 mL/min/1.73 m(2) four weeks after transplantation (relative risk, 4.3; P<0.001; sensitivity, 0.92; 95% CI, 0.77 to 0.98; specificity, 0.48; 95% CI, 0.31 to 0.66). Higher urinary calprotectin concentrations predicted impaired kidney function 4 weeks after transplantation, as well as 6 months and 12 months after transplantation. When data were analyzed using the urinary calprotectin/creatinine-ratio similar results were obtained. Urinary calprotectin was superior to current use of absolute change of plasma creatinine to predict allograft function 12 months after transplantation. Urinary calprotectin predicted an increased risk both in transplants from living and deceased donors. Multivariate linear regression showed that higher urinary calprotectin concentrations and older donor age predicted lower eGFR four weeks, 6 months, and 12 months after transplantation.

Conclusions: Urinary calprotectin is an early, noninvasive predictor of immediate renal allograft injury after kidney transplantation.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Allografts*
  • Female
  • Glomerular Filtration Rate
  • Humans
  • Kidney / pathology*
  • Kidney / physiopathology*
  • Kidney Transplantation / adverse effects
  • Leukocyte L1 Antigen Complex / urine*
  • Male
  • Middle Aged
  • Patient Outcome Assessment
  • Prognosis
  • Prospective Studies
  • ROC Curve
  • Risk Factors
  • Time Factors
  • Tissue Donors
  • Transplantation, Homologous

Substances

  • Leukocyte L1 Antigen Complex

Grants and funding

This work was supported by Deutsche Forschungsgemeinschaft (German Research Foundation, Research Unit FOR 1368) and the European Union (Interreg 4A, grant number 62-1.2-10). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.