IL-17 gene polymorphism (rs763780) in kidney recipients with post-transplant diabetes

IF 0.2 Q4 UROLOGY & NEPHROLOGY Journal of Renal Injury Prevention Pub Date : 2022-04-24 DOI:10.34172/jrip.2022.31976
S. Zununi Vahed, J. Etemadi, T. Majidi, S. M. Hejazian, Paria Ronaghi, M. Ardalan
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Abstract

Introduction: New-onset diabetes mellitus after transplantation (NODAT) is a common complication of organ transplantation, leading to allograft dysfunction. Genetic alterations of inflammatory cytokines have been reported to be associated with glucose homeostasis and diabetes. Objectives: This study evaluated the rs763780 polymorphism of IL-17F gene in transplant recipients with and without NODAT. Patients and Methods: The present retrospective study was conducted on ninety-one patients who have had a kidney transplant for at least three months. Patients were divided into two subgroups; recipients with NODAT (n=32) and kidney recipients without NODAT (n=59). After DNA extraction from patients’ blood samples, amplification and evaluation of specific polymorphism of the gene were performed using amplification refractory mutation system-polymerase chain reaction (ARMS-PCR). Clinical and demographic data of patients were collected. Results: The NODAT was detected in 81.3% (n=26) of TT genotype carriers, 12.5% of TC genotype carriers and 6.3% of CC genotype carriers. No statistically significant differences between the studied groups in the frequency of C and T alleles and the distribution of the abovementioned genotypes were detected (P≥0.721). In the NODAT group, graft rejection and age of patients were higher significantly (P≤0.017). Conclusion: No significant correlation between the incidence of diabetes and rs763780 polymorphism of IL-17F gene was observed.
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肾移植后糖尿病患者IL-17基因多态性(rs763780
引言:移植后新发糖尿病(NODAT)是器官移植的常见并发症,可导致移植物功能障碍。据报道,炎症细胞因子的基因改变与葡萄糖稳态和糖尿病有关。目的:本研究评估了IL-17F基因rs763780多态性在伴有和不伴有NODAT的移植受者中的表达。患者和方法:本回顾性研究对91例肾移植至少三个月的患者进行了研究。将患者分为两个亚组;NODAT受体(n=32)和无NODAT的肾受体(n=59)。从患者血液样本中提取DNA后,使用扩增难治性突变系统聚合酶链式反应(ARMS-PCR)对该基因的特异性多态性进行扩增和评估。收集患者的临床和人口统计数据。结果:在81.3%(n=26)的TT基因型携带者、12.5%的TC基因型携带者和6.3%的CC基因型携带者中检测到NODAT。研究组间C、T等位基因频率及上述基因型分布无统计学差异(P≥0.721),结论:IL-17F基因rs763780多态性与糖尿病发病率无显著相关性。
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来源期刊
Journal of Renal Injury Prevention
Journal of Renal Injury Prevention UROLOGY & NEPHROLOGY-
CiteScore
1.60
自引率
0.00%
发文量
36
期刊介绍: The Journal of Renal Injury Prevention (JRIP) is a quarterly peer-reviewed international journal devoted to the promotion of early diagnosis and prevention of renal diseases. It publishes in March, June, September and December of each year. It has pursued this aim through publishing editorials, original research articles, reviews, mini-reviews, commentaries, letters to the editor, hypothesis, case reports, epidemiology and prevention, news and views and renal biopsy teaching point. In this journal, particular emphasis is given to research, both experimental and clinical, aimed at protection/prevention of renal failure and modalities in the treatment of diabetic nephropathy. A further aim of this journal is to emphasize and strengthen the link between renal pathologists/nephropathologists and nephrologists. In addition, JRIP welcomes basic biomedical as well as pharmaceutical scientific research applied to clinical nephrology. Futuristic conceptual hypothesis that integrate various fields of acute kidney injury and renal tubular cell protection are encouraged to be submitted.
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