Król-Kulikowska Magdalena, Banasik Mirosław, Kepinska Marta
Department of Pharmaceutical Biochemistry, Faculty of Pharmacy, Wroclaw Medical University, Borowska 211a, 50-556 Wroclaw, Poland.
Department and Clinic of Nephrology and Transplantation Medicine, Faculty of Medicine, Wroclaw Medical University, Borowska 213, 50-556 Wroclaw, Poland.
Antioxidants (Basel). 2024 Jul 13;13(7):838. doi: 10.3390/antiox13070838.
Nitric oxide synthase (NOS) is an enzyme that catalyzes the formation of nitric oxide (NO), the altered production of which is characteristic of diabetic nephropathy. NOS exists in three isoforms: NOS1, NOS2, and NOS3. Moreover, there are reports about the potential role of polymorphisms in the development of diabetes complications. The aim of this study was to assess the role of selected polymorphisms-rs3782218 (), rs1137933 (), rs1799983, rs2070744, and rs61722009 ()-in the risk of developing diabetic nephropathy and in the likelihood of renal replacement therapy.
The studied polymorphisms were analyzed in a group of 232 patients divided into three groups. Four polymorphisms (rs3782218, rs1137933, rs1799983, rs2070744) were genotyped using the PCR-RFLP, while the rs61722009 polymorphism was genotyped using the PCR.
The C/C genotype and the C allele of the rs3782218 polymorphism () were associated with an increased risk of developing diabetic nephropathy and an increased likelihood of renal replacement therapy. In turn, the G allele of the rs1137933 polymorphism () reduces the likelihood of renal replacement therapy.
The specific genotypes or alleles of the rs3782218 () and rs1137933 () polymorphisms seem to be potential risk factors for diabetic nephropathy and renal replacement therapy.
一氧化氮合酶(NOS)是一种催化一氧化氮(NO)形成的酶,其生成改变是糖尿病肾病的特征。NOS存在三种亚型:NOS1、NOS2和NOS3。此外,有报道称多态性在糖尿病并发症发展中具有潜在作用。本研究的目的是评估所选多态性——rs3782218()、rs1137933()、rs1799983、rs2070744和rs61722009()——在糖尿病肾病发生风险及肾脏替代治疗可能性方面的作用。
在一组232例患者中分析所研究的多态性,这些患者被分为三组。使用聚合酶链反应-限制性片段长度多态性方法(PCR-RFLP)对四种多态性(rs3782218、rs1137933、rs1799983、rs2070744)进行基因分型,而rs61722009多态性使用聚合酶链反应(PCR)进行基因分型。
rs3782218多态性()的C/C基因型和C等位基因与糖尿病肾病发生风险增加及肾脏替代治疗可能性增加相关。反过来,rs1137933多态性()的G等位基因降低了肾脏替代治疗的可能性。
rs3782218()和rs1137933()多态性的特定基因型或等位基因似乎是糖尿病肾病和肾脏替代治疗的潜在危险因素。