Marre M, Hadjadj S, Bouhanick B
Diabetes Departments, Hôpital Bichat, Paris, France.
Diabetes Metab. 2000 Jul;26 Suppl 4:30-6.
The role of genetics in diabetic renal disease has been suspected on the basis of follow-up and familial studies. Barely half of Type 1 patients who develop a diabetic retinopathy also develop nephropathy, and the relative risk of nephropathy for a diabetic proband is around 3 if a sib is affected. Candidate genes for diabetic nephropathy can be divided into two categories: those affecting glucose metabolism in target organs of diabetic microangiopathy, and those affecting renal changes in response to hyperglycaemia. The role of angiotensin-I-converting enzyme (ACE) insertion/deletion (I/D) polymorphism has been suspected for several years. Evidence of its possible role in the development and progression of diabetic renal disease is presented here.
基于随访研究和家族研究,人们怀疑遗传学在糖尿病肾病中发挥作用。在患有糖尿病视网膜病变的1型糖尿病患者中,仅有半数左右会发展为肾病,若先证者的同胞患有肾病,那么该先证者患肾病的相对风险约为3。糖尿病肾病的候选基因可分为两类:一类影响糖尿病微血管病变靶器官中的葡萄糖代谢,另一类影响肾脏对高血糖的反应变化。血管紧张素转换酶(ACE)插入/缺失(I/D)多态性的作用已被怀疑数年。本文展示了其在糖尿病肾病发生和发展中可能发挥作用的证据。