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糖尿病患者的肾脏受累及疾病

Kidney involvement and disease in patients with diabetes.

作者信息

Chiarelli F, Trotta D, Verrotti A, Mohn A

机构信息

Department of Paediatrics, University of Chieti, Chieti, Italy.

出版信息

Panminerva Med. 2003 Mar;45(1):23-41.

Abstract

Diabetic nephropathy is the leading cause of end-stage renal disease in western or westernised countries and the largest contributor to the total cost of diabetes care around the world. In addition to the development of diabetic nephropathy and end-stage renal failure, diabetic patients with evidence of albuminuria have a much higher risk of developing myocardial infarctions, cerebrovascular accidents, severe progressive retinopathy, and peripheral and autonomic neuropathy. A cumulative incidence of diabetic nephropathy has been documented after duration of diabetes of at least 25 years in both type 1 and type 2 diabetic patients, although more recent studies have demonstrated a substantial reduction of its incidence. Before the onset of overt proteinuria, there are several renal functional changes, including renal hyperfiltration, hyperperfusion, and increasing capillary permeability to macromolecules. Basement-membrane thickening and mesangial expansion have long been recognized as pathological hallmark of diabetic nephropathy. It has been postulated that diabetic nephropathy occurs as a result of the interplay of metabolic and haemodynamic factors in the renal microcirculation. Hyperglycaemia plays a pivotal role in the pathogenesis of diabetic renal disease, but genetic factors are also of crucial importance. The accumulation of advanced glycosilation end products (AGEPs), the activation of isoforms of protein kinase C (PKC) and the acceleration of the aldose reductase pathway may explain how hyperglycaemia damages vessels. Growth factors (i.e. TGF-b, IGF-1, VEGF) may also play an important role in the pathogenesis. There is a familial clustering of diabetic kidney disease: a number of gene loci have been investigated to try to explain the genetic susceptibility to this complication. The two main treatment strategies for prevention of diabetic nephropathy are improved glycaemic control and blood pressure lowering, particularly using drugs such angiotensin-converting enzyme inhibitors and angiotensin II receptor antagonists. Many potential treatment modalities in preventing and treating diabetic nephropathy are presently being evaluated; some of them will possibly be available in the near future in order to try to modify the natural course of kidney involvement and disease in patients with diabetes.

摘要

糖尿病肾病是西方或西方化国家终末期肾病的主要病因,也是全球糖尿病治疗总成本的最大贡献因素。除了糖尿病肾病和终末期肾衰竭的发生,有蛋白尿证据的糖尿病患者发生心肌梗死、脑血管意外、严重进行性视网膜病变以及周围和自主神经病变的风险要高得多。1型和2型糖尿病患者在糖尿病病程至少25年后均有糖尿病肾病累积发病率的记录,尽管最近的研究表明其发病率已大幅降低。在显性蛋白尿出现之前,有几种肾功能变化,包括肾高滤过、高灌注以及毛细血管对大分子通透性增加。基底膜增厚和系膜扩张长期以来一直被认为是糖尿病肾病的病理标志。据推测,糖尿病肾病是肾微循环中代谢和血流动力学因素相互作用的结果。高血糖在糖尿病肾病发病机制中起关键作用,但遗传因素也至关重要。晚期糖基化终产物(AGEPs)的积累、蛋白激酶C(PKC)同工型的激活以及醛糖还原酶途径的加速可能解释了高血糖如何损害血管。生长因子(如转化生长因子-β、胰岛素样生长因子-1、血管内皮生长因子)在发病机制中也可能起重要作用。糖尿病肾病存在家族聚集性:人们已经研究了多个基因位点,试图解释对这种并发症的遗传易感性。预防糖尿病肾病的两种主要治疗策略是改善血糖控制和降低血压,特别是使用血管紧张素转换酶抑制剂和血管紧张素II受体拮抗剂等药物。目前正在评估许多预防和治疗糖尿病肾病的潜在治疗方式;其中一些可能在不久的将来可用,以便试图改变糖尿病患者肾脏受累和疾病的自然病程。

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