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Diabetic nephropathy; clinical stage and prediction

机译:糖尿病肾病;临床阶段和预测

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Diabetic nephropathy(DN) is the leading cause of end-stage renal disease in Japan. Clinical course of DN is divided into five stages. Stage 1 is a pre-nephropathy stage. Stage 2 is the period with microalbuminuria. Stage 3A is the stage with persistent macroproteinuria and well preserved renal function. Strict glycemic control and antihypertensive treatment with ACE inhibitors are capable of inducing remission in stage 2 of DN and probably in stage 3A. GFR less than 60 ml/min and urinary protein excretion more than 1 g/day are regarded as stage 3B. Serum creatinine concentration increases in stage 4. Antihypertensive therapy and low protein diet are major options of therapy both in stage 3B and 4. Stage 5 is the period with renal replacement therapy. Survival rate of patients on HD due to DN still remains unsatisfactory. Only 30-50% of type 2 diabetic patients develop DN, suggesting that there are several factors other than hyperglycemia which induce DN. Prediabetic hypertension and parenteral hypertension are regarded as predictors of DN. Smoking, male gender, and advanced age might be risk factors of DN. Recently it was demonstrated that insertion/deletion(I/D) polymorphism of angiotensin converting enzyme gene is associated with DN. In addition polymorphisms of several genes seem to be associated with DN. Development of DNA tips will make it possible to determine a number of gene polymorphisms. Accumulations of the information on gene polymorphisms from many patients with or without DN are expected to contribute detection of patients at high risk of developing DN.
机译:糖尿病肾病(DN)是日本终末期肾脏疾病的主要原因。 DN的临床过程分为五个阶段。 1期是肾病前期。第二阶段是微量白蛋白尿期。 3A期是持续性大蛋白尿和肾功能良好保存的阶段。严格的血糖控制和ACE抑制剂抗高血压治疗能够在DN的第2阶段以及可能在3A阶段诱导缓解。 GFR小于60 ml / min,尿蛋白排泄大于1 g / day被视为3B期。血清肌酐浓度在第4阶段增加。在3B和4阶段,降压治疗和低蛋白饮食是主要的治疗选择。第5阶段是进行肾脏替代治疗的阶段。 DN引起的HD患者的存活率仍然不能令人满意。 2型糖尿病患者中只有30-50%会发生DN,这表明除了高血糖症之外,还有其他多种因素可诱发DN。糖尿病前期高血压和肠胃外高血压被认为是DN的预测指标。吸烟,男性和高龄可能是DN的危险因素。最近证实血管紧张素转化酶基因的插入/缺失(I / D)多态性与DN有关。另外,几个基因的多态性似乎与DN有关。 DNA尖端的发展将使确定许多基因多态性成为可能。预期来自许多患有或不患有DN的患者的基因多态性信息的积累将有助于发现处于发展DN高风险中的患者。

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