Conway Bryan R, Martin Rosalind, McKnight Amy-Jayne, Savage David A, Brady Hugh R, Maxwell Alexander P
Nephrology Research Group, Queen's University of Belfast, Northern Ireland.
Nephrol Dial Transplant. 2004 Aug;19(8):2019-24. doi: 10.1093/ndt/gfh342. Epub 2004 Jun 8.
There is substantial evidence for genetic susceptibility to diabetic nephropathy. In particular, genes that predispose to hypertension in the general population may confer susceptibility to nephropathy in patients with diabetes. A Gly460Trp variant in the alpha-adducin gene has been associated with essential hypertension. Our aim was to screen the alpha-adducin gene for polymorphisms and to determine if any variants predisposed patients with diabetes to nephropathy. A secondary objective was to assess for association between the Gly460Trp variant and hypertension.
The exons of the alpha-adducin gene were resequenced in 30 individuals. Selected variants were then genotyped in 155 patients with type 1 diabetes and nephropathy (cases) and 216 persons with type 1 diabetes but no evidence of nephropathy (controls) from Northern Ireland and in 95 cases and 118 controls from the Irish Republic.
Eleven polymorphisms were detected, of which six were novel and three caused amino-acid substitutions. The Gly460Trp and a novel Ser617Cys polymorphism were in strong linkage disequilibrium (D' = 0.98). Neither the genotype nor allele frequencies for the Gly460Trp polymorphism (P = 0.89 and 0.93 respectively) or the Ser617Cys polymorphism (P = 0.46 and 0.76) were significantly different between cases and controls when the Northern Ireland and Irish Republic sample groups were combined. Carriage of the 460Trp allele was not significantly associated with systolic or diastolic blood pressure in either the cases (P = 0.48 and 0.06, respectively) or in the controls (P = 0.50 and 0.94, respectively).
Variation in the alpha-adducin gene does not play a major role in the development of nephropathy in persons with type 1 diabetes in the Irish population. Furthermore, the Gly460Trp variant was not associated with hypertension in this population.
有大量证据表明糖尿病肾病存在遗传易感性。特别是,在普通人群中易患高血压的基因可能使糖尿病患者易患肾病。α - 内收蛋白基因中的Gly460Trp变异与原发性高血压有关。我们的目的是筛查α - 内收蛋白基因的多态性,并确定是否有任何变异使糖尿病患者易患肾病。第二个目标是评估Gly460Trp变异与高血压之间的关联。
对30名个体的α - 内收蛋白基因外显子进行重测序。然后对来自北爱尔兰的155例1型糖尿病合并肾病患者(病例组)和216例无肾病证据的1型糖尿病患者(对照组)以及来自爱尔兰共和国的95例病例和118例对照进行选定变异的基因分型。
检测到11种多态性,其中6种是新发现的,3种导致氨基酸替换。Gly460Trp和新发现的Ser617Cys多态性处于强连锁不平衡状态(D' = 0.98)。当将北爱尔兰和爱尔兰共和国的样本组合时,病例组和对照组之间Gly460Trp多态性的基因型频率(分别为P = 0.89和0.93)或等位基因频率(P = 0.46和0.76)以及Ser617Cys多态性均无显著差异。在病例组(分别为P = 0.48和0.06)或对照组(分别为P = 0.50和0.9)中,携带460Trp等位基因与收缩压或舒张压均无显著关联。
在爱尔兰人群中,α - 内收蛋白基因的变异在1型糖尿病患者肾病的发生中不起主要作用。此外,在该人群中,Gly460Trp变异与高血压无关。