AL-TURATH UNIVERSITY COLLEGE, BAGHDAD, IRAQ.
AL-NISOUR UNIVERSITY COLLEGE, BAGHDAD, IRAQ.
Wiad Lek. 2021;74(9 cz 2):2297-2300.
The aim: This study is designed to investigate the possible association of genetic polymorphism expression of UMOD gene and chronic kidney disease in population.
Materials and methods: In the current study, the single-nucleotide polymorphisms (SNPs) were genotyped in the promoter region of the UMOD gene in CKD patients to assess its association with the kidney outcome of CKD. So 50 patients' blood samples suffered from CKD were collected. Among these patients, 21 were men and 29 women, aged 35 - 85 years old. Another group included 50 healthy subjects. DNA was extracted from all blood samples with EDTA using Quick DNA miniprep Kit ZYMO, (Cat№ D3025) according to manufacturer's instructions. Genotyping of 1 common polymorphisms (rs4293393) of the UMOD gene was done and the RNA was extracted and converted to cDNA and a set of primers was used to amplify specific region within the UMOD gene; another set was used to amplify the GAPDH gene to use it in calculation as a reference gene.
Results and conclusions: After statistical analysis, the results showed that there could be association between having CC mutant polymorphism in UMOD gene and having CKD.
本研究旨在探讨 UMOD 基因遗传多态性表达与人群慢性肾脏病的可能关联。
在本研究中,对 CKD 患者 UMOD 基因启动子区域的单核苷酸多态性(SNPs)进行了基因分型,以评估其与 CKD 肾脏结局的关系。因此,收集了 50 名患有 CKD 的患者的血液样本。这些患者中,21 名为男性,29 名为女性,年龄在 35-85 岁之间。另一组包括 50 名健康受试者。所有血液样本均使用 EDTA 提取 DNA,采用 Quick DNA miniprep Kit ZYMO(Cat№ D3025),根据制造商的说明进行。对 UMOD 基因的 1 个常见多态性(rs4293393)进行基因分型,并提取 RNA 并转化为 cDNA,使用一组引物扩增 UMOD 基因内的特定区域;另一组引物用于扩增 GAPDH 基因,作为参考基因进行计算。
经过统计学分析,结果表明 UMOD 基因中 CC 突变多态性与 CKD 之间可能存在关联。