A 63bp deletion in the promoter of RAGE correlates with a decreased risk for nephropathy in patients with type 2 diabetes

被引:25
作者
Rudofsky, G
Isermann, B
Schilling, T
Schiekofer, S
Andrassy, M
Schneider, JG
Morcos, M
Humpert, PM
Sayed, AAR
Witte, S
Renn, W
Pfohl, M
Hamann, A
Nosikov, V
Schleicher, E
Häring, HU
Rudofsky, G
Ritz, E
Nawroth, PP
Bierhaus, A
机构
[1] Univ Heidelberg, Dept Med 1, Otto Meyerhof Zentrum, D-69120 Heidelberg, Germany
[2] Univ Heidelberg, Dept Nephrol, D-69120 Heidelberg, Germany
[3] Univ Heidelberg, Dept Med Biometry, Heidelberg, Germany
[4] Univ Tubingen, Dept Med 4, Tubingen, Germany
[5] Bethesda Klin Duisburg, Med Klin 1, Duisburg, Germany
[6] Natl Res Ctr, Dept Mol Diagnost & Genome Fingerprinting, Moscow, Russia
[7] Univ Essen Gesamthsch, Dept Angiol, Essen, Germany
关键词
diabetes mellitus; diabetic nephropathy receptor of advanced; glycation endproducts; polymorphism;
D O I
10.1055/s-2004-817822
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Several polymorphisms have been identified in the RAGE-promoter region that might modulate the outcome of disease. Here we analyse the association of a 63bp deletion (delta63) spanning from bp-407 to bp-345 with diabetic nephropathy. The deletion was determined using the polymerase chain reaction (PCR) in a cross-sectional study with 1087 patients with type 1 diabetes (n = 559) and type 2 diabetes (n = 528). 475 patients with osteoporosis served as disease independent control. The prevalence of the heterozygous genotype did not significantly differ between the three groups (type 1: 2.15%, type 2: 2.27%, controls: 1.47%), indicating that heterozygous delta63 is not related to the manifestation of diabetes. Homozygous carriers were not identified in this study. The heterozygous delta63 genotype, was associated with a reduced prevalence of diabetic nephropathy in patients with type 2 diabetes (OR = 0.06; 95% CI: [0.05, 0.07]), but not in patients with type 1 (OR = 1.49; 95% CI: [1.14, 1.94]). We conclude, that patients with type 2 diabetes and the 63bp deletion in the promoter of RAGE seem to be protected from diabetic nephropathy. The observed difference between type 1 and type 2 diabetes might point to diverse pathomechanisms of nephropathy in both types of diabetes.
引用
收藏
页码:135 / 141
页数:7
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