Survey of HLA Distribution in Patients with End Stage Renal Disease Secondary to Reflux Nephropathy

Introduction: To evaluate the human leukocyte antigen (HLA) types of patients with vesicoureteral reflux (VUR) who underwent renal transplantation for end-stage renal disease (ESRD) to investigate for any significant association.Methods: This retrospective study comprised 26 patients (male, 15; fema...

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Bibliographic Details
Published in:İstanbul Medical Journal Vol. 19; no. 3; pp. 255 - 257
Main Authors: Ozcan, Rahsan, Altinay Kirli, Elif, Kortan, Elif, Pekmezci, Salih, Seyahi, Nurhan, Yilmaz, Erkan, Canpolat, Nur, Altiparmak, Mehmet Riza, Elicevik, Mehmet
Format: Journal Article
Language:English
Published: Galenos Yayinevi 01-09-2018
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Summary:Introduction: To evaluate the human leukocyte antigen (HLA) types of patients with vesicoureteral reflux (VUR) who underwent renal transplantation for end-stage renal disease (ESRD) to investigate for any significant association.Methods: This retrospective study comprised 26 patients (male, 15; female, 11) with ESRD secondary to VUR (ESRD/VUR group) who underwent renal transplantation, and 38 healthy donors (female, 24; male, 14) were randomized in the control group. The Single Specific Primer-Polymerase Chain Reaction (low resolution) method was performed for HLA typing. The statistical analyses included chi-square test and calculation of odds ratio (OR).Results: The median age was 25.2 years (R, 10-41) in the ESRD/VUR group and 43.9 (R, 20-76) in the control group. A statistically significant difference between HLA A and B types was not observed. The HLA DRB1*01 was significantly higher in the ESRD/VUR group than in the control group (p=0,024). The OR for the HLA DRB1*01 was 2.727. The risk of developing ESRD secondary to VUR was 2.727 times higher in the presence of the HLA DRB1*01.Conclusion: An association between HLA DRB1*01 and ESRD secondary to VUR was established. The HLA DRB1*01 antigen could be interpreted as a poor prognostic factor of reflux nephropathy. This finding should be supported by further studies.
ISSN:2619-9793
2148-094X
DOI:10.5152/imj.2018.32748