首页> 外文期刊>Journal of Nephropathology >Study of the association between the donors and recipients angiotensin-converting enzyme insertion/deletion gene polymorphism and the acute renal allograft rejection
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Study of the association between the donors and recipients angiotensin-converting enzyme insertion/deletion gene polymorphism and the acute renal allograft rejection

机译:供体和受体血管紧张素转换酶插入/缺失基因多态性与急性同种异体移植排斥相关性的研究

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Background: Angiotensin converting enzyme (ACE) is involved in various pathophysiological conditions including renal function. ACE levels are under genetic control. Objectives: This study was designed to investigate the association between the donors and recipients ACE-I/D gene polymorphism and risk of acute rejection outcome in renal allograft recipients. Patients and Methods: ACE-I/D polymorphism was determined in 200 donor-recipient pairs who had been referred to Afzalipour hospital in Kerman. ACE-I/D polymorphism was detected using polymerase chain reaction (PCR). Acute rejection (AR) during at least six months post-transplantation was defined as a 20% increase in creatinine level from the postoperative baseline in the absence of other causes of graft dysfunction which responded to antirejection therapy. Results: The observed allele frequencies were II 9.8%, ID 35.6% and DD 44.4% in donors and II 9.8%, ID 35.1% and DD 52.7% in recipients. There were no significant association between ACE genotypes and AR episodes (ORID=0.96 [0.18-5.00] and ORDD: 1.24 [0.25-6.07] for the donors) and (ORID: 0.29 [0.06-1.45] and ORDD: 0.75 [0.19-2.90] for the recipients). Conclusions: It seems that donor and recipient ACE-I/D genotype might not be a risk factor for acute renal allograft rejection. However, due to conflicting results from this and other studies, multicenter collaborative studies with more participants and concomitant evaluation of ACE polymorphism with other polymorphisms in renin–angiotensin system (RAS) are suggested to determine whether ACE genotypes are significant predictors of renal allograft rejection.
机译:背景:血管紧张素转换酶(ACE)参与各种病理生理状况,包括肾功能。 ACE水平处于遗传控制之下。目的:本研究旨在研究供体和受体ACE-I / D基因多态性与同种异体肾移植受体急性排斥反应风险之间的关系。患者和方法:ACE-I / D基因多态性已在200名捐献者/接受者对中确定,他们已被转诊至Kerman的Afzalipour医院。使用聚合酶链反应(PCR)检测ACE-I / D多态性。移植后至少六个月内的急性排斥反应(AR)被定义为在没有其他原因引起的抗排斥治疗的移植物功能障碍的情况下,肌酐水平较术后基线水平增加了20%。结果:观察到的等位基因频率在供体中为II 9.8%,ID 35.6%和DD 44.4%,在接受者中为II 9.8%,ID 35.1%和DD 52.7%。 ACE基因型与AR发作之间没有显着相关性(供体的ORID = 0.96 [0.18-5.00]和ORDD:1.24 [0.25-6.07])和(ORID:0.29 [0.06-1.45]和ORDD:0.75 [0.19- 2.90]。结论:似乎供体和受体ACE-I / D基因型可能不是急性肾移植排斥反应的危险因素。但是,由于这项研究与其他研究结果相矛盾,因此建议进行更多参与者的多中心协作研究,并同时评估ACE多态性与肾素-血管紧张素系统(RAS)中的其他多态性,以确定ACE基因型是否是移植肾排斥的重要预测因子。

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