Risk genotypes and haplotypes of the GLUT1 gene for type 2 diabetic nephropathy in the Tunisian population

被引:10
作者
Makni, K. [1 ]
Jarraya, F. [1 ,2 ]
Rebai, M. [3 ]
Mnif, F. [4 ]
Boudawara, M. [5 ]
Hamza, N. [5 ]
Rekik, N. [4 ]
Abid, M. [4 ]
Hachicha, J. [2 ]
Granier, C. [6 ]
Rebai, A. [3 ]
Ayadi, H. [1 ]
机构
[1] Ctr Biotechnol Sfax, Res Unit Target Diag & Therapeut Human Pathol, Sfax, Tunisia
[2] Hedi Chaker Hosp, Dept Nephrol, Sfax, Tunisia
[3] Ctr Biotechnol Sfax, Res Unit Bioinformat, Sfax, Tunisia
[4] Hedi Chaker Hosp, Dept Endocrinol, Sfax, Tunisia
[5] Social Natl Case Sfax, Lab Anal, Sfax, Tunisia
[6] Fac Pharm Montpellier, Ctr Pharmacol & Biotechnol Hlth,CNRS,UMR 5094, CNRS,BIO RAD, FRE 3009, Montpellier, France
关键词
diabetic nephropathy; GLUT1; gene; risk haplotype;
D O I
10.1080/03014460802247142
中图分类号
Q98 [人类学];
学科分类号
030303 ;
摘要
Objective: Diabetic nephropathy (DN) is a long-term complication of both type 1 and type 2 diabetes. Genetic studies on DN have been of little help so far, since several genetic association studies have shown conflicting results. Here we report the findings of a case-control study on five SNPs in the glucose transporter 1 (GLUT1) gene. The study investigated the association of five GLUT1 genotypes and haplotypes with DN. Research design and methods: All subjects, 126 DN (cases) and 273 type 2 diabetes (controls), were genotyped using the polymerase chain reaction restriction fragment length polymorphism. Results: The TT and the AA genotypes of the Haell and Enh2 SNP1, increased the risk of DN. The study also identified CGT as the highest risk haplotype (4.4-fold) followed by CAT with an increased risk of DN of 2.6-fold. Conclusions: The GLUT1 gene confers susceptibility to DN in type 2 diabetes patients in the Tunisian population.
引用
收藏
页码:490 / 498
页数:9
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