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

被引:1
|
作者
Sortica, Denise A. [1 ,2 ]
Crispim, Daisy [1 ,2 ]
Bauer, Andrea C. [2 ,3 ]
Nique, Pamela S. [1 ,2 ]
Nicoletto, Bruna B. [1 ,4 ,5 ]
Crestani, Ricieli P. [1 ]
Staehler, Jennifer T. [1 ]
Manfro, Roberto C. [3 ]
Canani, Luis H. [1 ,2 ]
机构
[1] Hosp Clin Porto Alegre, Endocrine Div, Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Fac Med, Postgrad Program Med Sci Endocrinol, Porto Alegre, RS, Brazil
[3] Hosp Clin Porto Alegre, Div Nephrol, Porto Alegre, RS, Brazil
[4] Univ Caxias Do Sul, Life Sci Knowledge Area, Caxias Do Sul, RS, Brazil
[5] UCS, Nutr Course, Area Conhecimento Ciencias Vida, Caxias Do Sul, RS, Brazil
来源
PLOS ONE | 2019年 / 14卷 / 07期
关键词
GLYCOPROTEIN PC-1 GENE; ADENOSINE GENERATION; CLASSIFICATION; CD73; RISK; IMMUNOSUPPRESSION; TRANSPLANTATION; IDENTIFICATION; NUCLEOTIDES; EXPRESSION;
D O I
10.1371/journal.pone.0219062
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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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页数:12
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