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K121Q polymorphism in the Ectonucleotide Pyrophosphatase/Phosphodiesterase 1 gene is associated with acute kidney rejection

The identification of risk factors for acute rejection (AR) may lead to strategies to improve success of kidney transplantation. Ectonucleotidases are ectoenzymes that hydrolyze extracellular nucleotides into nucleosides, modulating the purinergic signaling. Some members of the Ectonucleotidase fami...

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Autores principales: Sortica, Denise A., Crispim, Daisy, Bauer, Andrea C., Nique, Pamela S., Nicoletto, Bruna B., Crestani, Ricieli P., Staehler, Jennifer T., Manfro, Roberto C., Canani, Luis H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639061/
https://www.ncbi.nlm.nih.gov/pubmed/31318911
http://dx.doi.org/10.1371/journal.pone.0219062
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author Sortica, Denise A.
Crispim, Daisy
Bauer, Andrea C.
Nique, Pamela S.
Nicoletto, Bruna B.
Crestani, Ricieli P.
Staehler, Jennifer T.
Manfro, Roberto C.
Canani, Luis H.
author_facet Sortica, Denise A.
Crispim, Daisy
Bauer, Andrea C.
Nique, Pamela S.
Nicoletto, Bruna B.
Crestani, Ricieli P.
Staehler, Jennifer T.
Manfro, Roberto C.
Canani, Luis H.
author_sort Sortica, Denise A.
collection PubMed
description The identification of risk factors for acute rejection (AR) may lead to strategies to improve success of kidney transplantation. Ectonucleotidases are ectoenzymes that hydrolyze extracellular nucleotides into nucleosides, modulating the purinergic signaling. Some members of the Ectonucleotidase family have been linked to transplant rejection processes. However, the association of Ectonucleotide Pyrophosphatase / Phosphodiesterase 1 (ENPP1) with AR has not yet been evaluated. The aim of this study was to evaluate the association between the K121Q polymorphism of ENPP1 gene and AR in kidney transplant patients. We analyzed 449 subjects without AR and 98 with AR from a retrospective cohort of kidney transplant patients from Southern Brazil. K121Q polymorphism was genotyped using allelic discrimination-real-time PCR. Cox regression analysis was used to evaluate freedom of AR in kidney transplant patients according to genotypes. Q allele frequency was 17.6% in recipients without AR and 21.9% in those with AR (P = 0.209). Genotype frequencies of the K121Q polymorphism were in Hardy-Weinberg equilibrium in non-AR patients (P = 0.70). The Q/Q genotype (recessive model) was associated with AR (HR = 2.83, 95% CI 1.08–7.45; P = 0.034) after adjusting for confounders factors. Our findings suggest a novel association between the ENPP1 121Q/Q genotype and AR in kidney transplant recipients.
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spelling pubmed-66390612019-07-25 K121Q polymorphism in the Ectonucleotide Pyrophosphatase/Phosphodiesterase 1 gene is associated with acute kidney rejection Sortica, Denise A. Crispim, Daisy Bauer, Andrea C. Nique, Pamela S. Nicoletto, Bruna B. Crestani, Ricieli P. Staehler, Jennifer T. Manfro, Roberto C. Canani, Luis H. PLoS One Research Article The identification of risk factors for acute rejection (AR) may lead to strategies to improve success of kidney transplantation. Ectonucleotidases are ectoenzymes that hydrolyze extracellular nucleotides into nucleosides, modulating the purinergic signaling. Some members of the Ectonucleotidase family have been linked to transplant rejection processes. However, the association of Ectonucleotide Pyrophosphatase / Phosphodiesterase 1 (ENPP1) with AR has not yet been evaluated. The aim of this study was to evaluate the association between the K121Q polymorphism of ENPP1 gene and AR in kidney transplant patients. We analyzed 449 subjects without AR and 98 with AR from a retrospective cohort of kidney transplant patients from Southern Brazil. K121Q polymorphism was genotyped using allelic discrimination-real-time PCR. Cox regression analysis was used to evaluate freedom of AR in kidney transplant patients according to genotypes. Q allele frequency was 17.6% in recipients without AR and 21.9% in those with AR (P = 0.209). Genotype frequencies of the K121Q polymorphism were in Hardy-Weinberg equilibrium in non-AR patients (P = 0.70). The Q/Q genotype (recessive model) was associated with AR (HR = 2.83, 95% CI 1.08–7.45; P = 0.034) after adjusting for confounders factors. Our findings suggest a novel association between the ENPP1 121Q/Q genotype and AR in kidney transplant recipients. Public Library of Science 2019-07-18 /pmc/articles/PMC6639061/ /pubmed/31318911 http://dx.doi.org/10.1371/journal.pone.0219062 Text en © 2019 Sortica et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sortica, Denise A.
Crispim, Daisy
Bauer, Andrea C.
Nique, Pamela S.
Nicoletto, Bruna B.
Crestani, Ricieli P.
Staehler, Jennifer T.
Manfro, Roberto C.
Canani, Luis H.
K121Q polymorphism in the Ectonucleotide Pyrophosphatase/Phosphodiesterase 1 gene is associated with acute kidney rejection
title K121Q polymorphism in the Ectonucleotide Pyrophosphatase/Phosphodiesterase 1 gene is associated with acute kidney rejection
title_full K121Q polymorphism in the Ectonucleotide Pyrophosphatase/Phosphodiesterase 1 gene is associated with acute kidney rejection
title_fullStr K121Q polymorphism in the Ectonucleotide Pyrophosphatase/Phosphodiesterase 1 gene is associated with acute kidney rejection
title_full_unstemmed K121Q polymorphism in the Ectonucleotide Pyrophosphatase/Phosphodiesterase 1 gene is associated with acute kidney rejection
title_short K121Q polymorphism in the Ectonucleotide Pyrophosphatase/Phosphodiesterase 1 gene is associated with acute kidney rejection
title_sort k121q polymorphism in the ectonucleotide pyrophosphatase/phosphodiesterase 1 gene is associated with acute kidney rejection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639061/
https://www.ncbi.nlm.nih.gov/pubmed/31318911
http://dx.doi.org/10.1371/journal.pone.0219062
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