Abstract

ABSTRACTIntroduction:The development of novel non-invasive biomarkers of kidney graft dysfunction, especially in the course of the delayed graft function period would be an important step forward in the clinical practice of kidney transplantation.Methods:We evaluated by RT-PCR the expression of miRNA-146 to -5p ribonucleic micro-acids (miRNAs) in the peripheral blood and renal tissue obtained from kidney transplant recipients who underwent a surveillance graft biopsy during the period of delayed graft function.Results:In biopsy samples, the expression of miR-146a-5p was significantly increased in the group of patients with delayed graft function (DGF) (n = 33) versus stables patients (STA) (n = 13) and patients with acute rejection (AR) (n = 9) (p = 0.008). In peripheral blood samples, a non-significant increase of miR-146a-5p expression was found in the DGF group versus STA and AR groups (p = 0.083). No significant correlation was found between levels of expression in biopsy and plasma. ROC curve analysis revealed an AUC of 0.75 (95% CI: 0.62-0.88) for the renal tissue expression and 0.67 (95% CI 0.52-0.81) for the peripheral blood expression.Conclusion:We conclude that miR-146a-5p expression has a distinct pattern in the renal tissue and perhaps in the peripheral blood in the setting of DGF. Further refinements and strategies for studies should be developed in the field of non-invasive molecular diagnosis of kidney graft dysfunction.

Highlights

  • The development of novel non-invasive biomarkers of kidney graft dysfunction, especially in the course of the delayed graft function period would be an important step forward in the clinical practice of kidney transplantation

  • We evaluated by reverse transcription polymerase chain reaction (RT-PCR) the expression of miRNA-146 to -5p ribonucleic micro-acids in the peripheral blood and renal tissue obtained from kidney transplant recipients who underwent a surveillance graft biopsy during the period of delayed graft function

  • Serum creatinine was significantly elevated in the delayed graft function (DGF) group and time to biopsy was longer in the DGF group compared to the stable group

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Summary

Introduction

The development of novel non-invasive biomarkers of kidney graft dysfunction, especially in the course of the delayed graft function period would be an important step forward in the clinical practice of kidney transplantation. Results: In biopsy samples, the expression of miR-146a-5p was significantly increased in the group of patients with delayed graft function (DGF) (n = 33) versus stables patients (STA) (n = 13) and patients with acute rejection (AR) (n = 9) (p = 0.008). A non-significant increase of miR-146a-5p expression was found in the DGF group versus STA and AR groups (p = 0.083). As evidenced since the beginning of organ transplants, tissues and organs of genetically distinct individuals lose their functions through a rejection process that is mediated by the immune system Such process is only partially controlled by modifying the receptor immune response with immunosuppressive drugs and biological agents[3,4,5]. It is believed that these injuries facilitate mechanisms of acute rejection (AR) and act by programming gene, metabolic, and tissue changes that culminate in tissue graft fibrosis and chronic loss of function[8,9]

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