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Submitted: 22 Jan 2021
Accepted: 01 Aug 2021
ePublished: 29 Aug 2021
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J Renal Inj Prev. 2021;10(4): e30.
doi: 10.34172/jrip.2021.30

Scopus ID: 85115663103
  Abstract View: 1762
  PDF Download: 886

Original

Evaluation the performance of serum neutrophil gelatinase associated lipocalin as a biomarker of allograft dysfunction in kidney recipients from living donors

Elham Adlravan 1 ORCID logo, Farid Javandoust Gharehbagh 1 ORCID logo, Ali Taghizadeh Afshari 2, Behzad Baradaran 3 ORCID logo, Jaffar Nourooz-Zadeh 2,1* ORCID logo

1 Department of Clinical Biochemistry, Urmia University of Medical Sciences, Urmia, Iran
2 Nephrology and Kidney Transplant Research Center, Clinical Research Institute, Urmia University of Medical Sciences, Urmia, Iran
3 Immunology Research Center, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
*Corresponding Author: *Corresponding author: Professor Jaffar Nourooz-Zadeh, Email: jnouroozzadeh@yahoo.co.uk, , Email: nouroozzadeh.j@umsu.ac.ir

Abstract

Introduction: Serum neutrophil gelatinase-associated lipocalin (sNGAL) has been proposed as an early biomarker for the prediction of delayed graft function (DGF) from cadaveric donors.

Objectives: The purposes of this investigation were to explore the time-based trend for sNGAL in kidney recipients from living donors and to evaluate its correlation with graft function recovery during a one-year follow-up.

Patients and Methods: Kidney recipients (n=39) were consecutively enrolled. Sample collection was performed before transplantation and at 2, 16, 24, 36, 48 hours after surgery. Kidney recipients were split into immediate graft function (IGF) and DGF based on estimated glomerular filtration rate (eGFR) on day 5 post-surgery. eGFRs >60 mL/min/1.73 m2 on day 5 post-transplantation were considered as IGF. sNGAL was assessed by ELISA. Serum creatinine (sCr) was measured by the Jaffe method.

Results: Rates of participants with IGF or DGF were 25 and 14, respectively. Pre-surgery, sNGAL levels in the DGF subset were 21% higher than that of the IGF group. At 2-hours checkpoint, area under curve, sensitivity, specificity and cut-off (ng/mL) for sNGAL were 0.73, 100%, 52% and 151.8. sNGAL levels correlated with allograft function at 6, 9 and 12 months post-transplantation (r=0.66; P=0.007; r=0.836; P=0.031 and r=0.93; P=0.016).

Conclusion: We have uncovered that monitoring sNGAL in kidney recipients is a useful biomarker for the evaluation of short- and long postoperative outcome in renal transplant patients from living donors. However, multicenter study with large samples-size is required to ascertain the usefulness of sNGAL as diagnostic tool for the evaluation of allograft dysfunction in renal transplant patients from living donors.



Implication for health policy/practice/research/medical education:

Evidence signifies that serum neutrophil gelatinase-associated lipocalin (sNGAL) is a reliable predictor of early graft function organ recipients from deceased donors. We aimed to evaluate the diagnostic performance of sNGAL for the prediction of early and long-term graft restoration in kidney recipients from living donors. Organ recipients (n=39) were consecutively enrolled. Serial measurements were performed before transplantation and at 2, 16, 24, 36, 48 hours after surgery. Immediate graft function (IGF) was defined as an estimated glomerular filtration rate (eGFR) >60 mL/min per 1.73 m2 on day 5 post-transplantation. We have uncovered that the value of sNGAL at 2- hours post-surgery correlates allograft function at 6, 9 and 12 months post-transplantation. Multicenter study with large samples size is required to ascertain the usefulness of sNGAL as a diagnostic tool for the prediction of allograft function in renal transplant patients from living donors.

Please cite this paper as: Adlravan E, Javandoust Gharehbagh F, Taghizadeh Afshari A, Baradaran B, Nourooz-Zadeh J. Evaluation the performance of serum neutrophil gelatinase associated lipocalin as a biomarker of allograft dysfunction in kidney recipients from living donors. J Renal Inj Prev. 2021; 10(4): e30. doi: 10.34172/jrip.2021.30.


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