Prediction of delayed graft function and long-term graft survival by serum and urinary neutrophil gelatinase-associated lipocalin during the early postoperative phase after kidney transplantation

PLoS One. 2018 Jan 5;13(1):e0189932. doi: 10.1371/journal.pone.0189932. eCollection 2018.

Abstract

Neutrophil gelatinase-associated lipocalin (NGAL) has emerged as an early marker protein for kidney dysfunction in various clinical settings. In this prospective study we evaluated serial changes of serum and urinary NGAL within the first 7 days after kidney transplantation in 170 consecutive recipients. The main focus of this study was to assess the performance of serum and urinary NGAL in the prediction of delayed graft function (DGF) and two-year graft and patient survival. Serum and urine samples of 170 patients undergoing primary kidney transplantation from October 2010 to December 2012 were prospectively collected from day 0 to 7. NGAL was analyzed by ELISA. Multivariate regression models, receiver-operating characteristics (ROC), and areas under ROC curves (AUC) were used to identify predictors of DGF. DGF occurred in 52 patients (30.6%). Serum (AUC = 0.869) and urinary NGAL (AUC = 0.872) on postoperative day (POD) 2 could accurately predict DGF compared to serum creatinine (AUC = 0.619). Multivariate analyses revealed donor age, serum and urinary NGAL significantly associated with DGF (p<0.001). Recipient age was the only significant factor in a cox regression model influencing two-year graft and patient survival. In conclusion, serum and urinary NGAL are early predictors of DGF after kidney transplantation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Delayed Graft Function*
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Graft Survival*
  • Humans
  • Kidney Transplantation*
  • Lipocalin-2 / blood*
  • Lipocalin-2 / urine*
  • Male
  • Middle Aged
  • Postoperative Period
  • Prospective Studies
  • Survival Analysis

Substances

  • LCN2 protein, human
  • Lipocalin-2

Grants and funding

This work was supported by grants from the Austrian Science Fund (FWF), P233240, https://www.fwf.ac.at/ (FA).