Serpin Family E Member 1 Tag Single-Nucleotide Polymorphisms in Patients with Diabetic Nephropathy: An Association Study and Meta-Analysis Using a Genetic Model-Free Approach

荟萃分析 舍宾 单核苷酸多态性 遗传学 糖尿病肾病 计算生物学 生物 联想(心理学) 基因型 医学 内科学 基因 心理学 心理治疗师
作者
Maria Tziastoudi,Efthimios Dardiotis,Georgios Pissas,Georgios Filippidis,Spyridon Golfinopoulos,Vasileios Siokas,Sophia V. Tachmitzi,Theodoros Eleftheriadis,Georgios M. Hadjigeorgiou,Evangelia E. Tsironi,Ioannis Stefanidis
出处
期刊:Genes [Multidisciplinary Digital Publishing Institute]
卷期号:12 (12): 1887-1887 被引量:6
标识
DOI:10.3390/genes12121887
摘要

Background: Many lines of evidence highlight the genetic contribution on the development of diabetic nephropathy (DN). One of the studied genes is SERPINE1 whose the role in the risk of developing DN remains questionable. In order to elucidate the contribution of SERPINE1 in DN progression in the context of type 2 diabetes mellitus (T2DM), we conducted an association study and meta-analysis of SERPINE1 genetic variants. Materials and Methods: A total of 190 patients with DN, 150 T2DM (type 2 diabetes mellitus) patients without DN and 238 healthy controls were recruited. We selected five tag single-nucleotide polymorphisms (SNPs) from the HapMap. The generalized odds ratio (ORG) was calculated to estimate the risk on DN development. Subgroup analyses based on ethnicity and type of diabetes were also performed. Results: Both the present association study regarding SERPINE1 SNPs (rs2227667, rs2070682, rs1050813, rs2227690, rs2227692) did not found any significant association between SERPINE1 variants and DN and the meta-analysis of variant 4G>5G (rs1799889) did not also reveal a significant association between 4G>5G variant and DN in main and subgroup analyses. Discussion: In conclusion, the present association study and meta-analysis provides strong evidence that SERPINE1 genetic variant 4G>5G is not implicated in the risk or development of DN in Caucasians. Further studies in other populations remain to further investigate the role of this variant in the course of DN.

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