Blumberg A
Schweiz Med Wochenschr. 1986 Mar 1;116(9):275-81.
Diabetic nephropathy due to glomerulosclerosis develops in 40% of patients with type I diabetes (in type II the incidence is only around 5%). Two mechanisms are of pathogenetic importance: hemodynamic changes with glomerular hyperfiltration leading to glomerulosclerosis and proteinuria, and biochemical alterations of the glomerular basement membrane consisting of an increase and glycosylation of collagen IV as well as a decrease in negatively charged proteoglycans and sialic acid. Diabetic nephropathy runs through several stages, the first being characterized by hyperfunction and hypertrophy. The appearance of microalbuminuria after 10-15 years of diabetes seems to be a good indicator of the later development of clinically overt nephropathy with large urinary protein losses and decreasing renal function. Successful treatment of hypertension may slow the decrease of renal function. For those patients who have reached terminal renal failure, the treatment modalities of hemodialysis, continuous ambulatory peritoneal dialysis (CAPD) and renal transplantation offer a reasonable chance of prolonging life, although the results are generally less good than in non-diabetic renal patients of the same age group. However, the ultimate goal of therapy must remain the successful prevention of the devastating late sequelae of diabetes, including diabetic nephropathy.
1型糖尿病患者中,40%会因肾小球硬化而发展为糖尿病肾病(2型糖尿病患者的发病率仅约为5%)。有两种发病机制具有重要意义:血流动力学改变伴肾小球高滤过,导致肾小球硬化和蛋白尿;肾小球基底膜的生化改变,包括IV型胶原增加和糖基化,以及带负电荷的蛋白聚糖和唾液酸减少。糖尿病肾病会经历几个阶段,第一阶段的特征是功能亢进和肥大。糖尿病10 - 15年后出现微量白蛋白尿似乎是临床显性肾病后期发展的良好指标,临床显性肾病会出现大量尿蛋白丢失和肾功能下降。成功控制高血压可能会减缓肾功能下降。对于那些已达到终末期肾衰竭的患者,血液透析、持续非卧床腹膜透析(CAPD)和肾移植等治疗方式为延长生命提供了合理的机会,尽管总体结果通常不如同年龄组的非糖尿病肾病患者。然而,治疗的最终目标必须仍然是成功预防糖尿病的毁灭性晚期后遗症,包括糖尿病肾病。