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Association of FAS -670A/G and FASL –843C/T Gene Polymorphisms on Allograft Nephropathy in Pediatric Renal Transplant Patients

OBJECTIVE: FAS and FASL polymorphisms are suggested to play an important role in tubulitis that is a major component of acute rejection. The aim of this study was to investigate the role of FAS-670A/G and FASL–843C/T gene polymorphisms on allograft nephropathy in pediatric renal transplant patients...

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Autores principales: Ertan, Pelin, Mir, Sevgi, Ozkayin, Nese, Berdeli, Afig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446084/
https://www.ncbi.nlm.nih.gov/pubmed/23056744
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author Ertan, Pelin
Mir, Sevgi
Ozkayin, Nese
Berdeli, Afig
author_facet Ertan, Pelin
Mir, Sevgi
Ozkayin, Nese
Berdeli, Afig
author_sort Ertan, Pelin
collection PubMed
description OBJECTIVE: FAS and FASL polymorphisms are suggested to play an important role in tubulitis that is a major component of acute rejection. The aim of this study was to investigate the role of FAS-670A/G and FASL–843C/T gene polymorphisms on allograft nephropathy in pediatric renal transplant patients METHODS: Fifty three patients (22 males 31 females) aged 2 to 20 years (mean 12.3±0.6) who had renal transplantation and fifty healthy control subjects (25 males 25 females) were enrolled in the study. Pearson's Chi Square test was used for the statistical analysis. Survival rates were estimated with the Kaplan Meier method. Age, sex, chronic renal failure etiology, treatment modality and duration and donor type were recorded. FAS-670A/G and FASL–843C/T gene polymorphisms were compared between renal transplant patients and normal healthy population as well as between renal transplant patients with and without acute rejection. FINDINGS: FAS-670A/G genotypes or alleles were not significantly different between control and transplant patients and among transplant patients with and without acute rejection (P>0.05 for all). FASL–843C/T genotypes and alleles were not different between transplantation and control groups (P>0.05 for all). However, FASL–843C/T alleles were significantly different between patients with and without AR (P=0.02). The percentages of C allele were higher in children with acute rejection (68.8% vs 44.6%). CONCLUSION: FASL gene polymorphisms may play a major role in acute rejection while FAS polymorphisms have not been found to be different between patients with and without acute renal graft rejection.
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spelling pubmed-34460842012-10-09 Association of FAS -670A/G and FASL –843C/T Gene Polymorphisms on Allograft Nephropathy in Pediatric Renal Transplant Patients Ertan, Pelin Mir, Sevgi Ozkayin, Nese Berdeli, Afig Iran J Pediatr Original Article OBJECTIVE: FAS and FASL polymorphisms are suggested to play an important role in tubulitis that is a major component of acute rejection. The aim of this study was to investigate the role of FAS-670A/G and FASL–843C/T gene polymorphisms on allograft nephropathy in pediatric renal transplant patients METHODS: Fifty three patients (22 males 31 females) aged 2 to 20 years (mean 12.3±0.6) who had renal transplantation and fifty healthy control subjects (25 males 25 females) were enrolled in the study. Pearson's Chi Square test was used for the statistical analysis. Survival rates were estimated with the Kaplan Meier method. Age, sex, chronic renal failure etiology, treatment modality and duration and donor type were recorded. FAS-670A/G and FASL–843C/T gene polymorphisms were compared between renal transplant patients and normal healthy population as well as between renal transplant patients with and without acute rejection. FINDINGS: FAS-670A/G genotypes or alleles were not significantly different between control and transplant patients and among transplant patients with and without acute rejection (P>0.05 for all). FASL–843C/T genotypes and alleles were not different between transplantation and control groups (P>0.05 for all). However, FASL–843C/T alleles were significantly different between patients with and without AR (P=0.02). The percentages of C allele were higher in children with acute rejection (68.8% vs 44.6%). CONCLUSION: FASL gene polymorphisms may play a major role in acute rejection while FAS polymorphisms have not been found to be different between patients with and without acute renal graft rejection. Tehran University of Medical Sciences 2010-12 /pmc/articles/PMC3446084/ /pubmed/23056744 Text en © 2010 Iranian Journal of Pediatrics & Tehran University of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution NonCommercial 3.0 License (CC BY-NC 3.0), which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Ertan, Pelin
Mir, Sevgi
Ozkayin, Nese
Berdeli, Afig
Association of FAS -670A/G and FASL –843C/T Gene Polymorphisms on Allograft Nephropathy in Pediatric Renal Transplant Patients
title Association of FAS -670A/G and FASL –843C/T Gene Polymorphisms on Allograft Nephropathy in Pediatric Renal Transplant Patients
title_full Association of FAS -670A/G and FASL –843C/T Gene Polymorphisms on Allograft Nephropathy in Pediatric Renal Transplant Patients
title_fullStr Association of FAS -670A/G and FASL –843C/T Gene Polymorphisms on Allograft Nephropathy in Pediatric Renal Transplant Patients
title_full_unstemmed Association of FAS -670A/G and FASL –843C/T Gene Polymorphisms on Allograft Nephropathy in Pediatric Renal Transplant Patients
title_short Association of FAS -670A/G and FASL –843C/T Gene Polymorphisms on Allograft Nephropathy in Pediatric Renal Transplant Patients
title_sort association of fas -670a/g and fasl –843c/t gene polymorphisms on allograft nephropathy in pediatric renal transplant patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3446084/
https://www.ncbi.nlm.nih.gov/pubmed/23056744
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