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蛋白尿:2型糖尿病肾病的治疗靶点。

Albuminuria: a target for treatment of type 2 diabetic nephropathy.

作者信息

de Zeeuw Dick

机构信息

Department of Clinical Pharmacology, University Medical Center Groningen, University of Groningen, Ant Deusinglaan 1, 9713 AV Groningen, the Netherlands.

出版信息

Semin Nephrol. 2007 Mar;27(2):172-81. doi: 10.1016/j.semnephrol.2007.01.002.

Abstract

Both renal and cardiovascular morbidity and mortality is increased markedly in patients with type 2 diabetes. Besides the classic risk factors and markers such as glucose, blood pressure, blood lipid profile, and lifestyle (smoking, overweight), novel risk markers are identified, among them urine albumin excretion. Levels of urinary albumin excretion greater than normal are observed frequently in patients with type 2 diabetes. Moderately increased levels of albuminuria, so-called microalbuminuria, are predictive both for progressive renal function loss to diabetic nephropathy, and for cardiovascular morbidity and mortality: the higher the albuminuria level, the more chance of renal and cardiovascular complications. More advanced levels of albuminuria (overt albuminuria) are observed in patients in the diabetic nephropathy state. In this condition, renal and cardiovascular risk are extremely high, and again one may observe that the level of albumin excretion is predictive of renal and cardiovascular outcome. Several drug strategies decrease the level of urinary albumin excretion in type 2 diabetic patients. Data on using drugs that intervene in the renin-angiotensin-aldosterone-system (RAAS) are the most extensive and conclusive. RAAS intervention is a very effective strategy to decrease the amount of albumin in the urine, independent from the blood pressure decreasing characteristics of the treatment. RAAS intervention is associated with long-term renal and cardiovascular protection. Importantly, the degree of short-term albuminuria decrease is associated with the degree of renal and cardiovascular protection: the more albuminuria reduction, the more protection. The protective predictive power of the albuminuria effect of RAAS intervention is not related to (or dissociated from) the blood pressure decreasing effect of these drugs. The protective effect of RAAS intervention is present at normoalbuminuric, microalbuminuric, and overt albuminuria levels. This makes albuminuria a target for therapy in type 2 diabetes. New drug strategies that decrease or prevent albuminuria without affecting other risk factors currently are being tested, and not only will add to underscoring the need to treat albuminuria as a separate target, but also will assist in reducing the enormous residual risk burden of individual diabetic patients.

摘要

2型糖尿病患者的肾脏和心血管疾病发病率及死亡率均显著增加。除了血糖、血压、血脂谱和生活方式(吸烟、超重)等经典危险因素和标志物外,还发现了新的风险标志物,其中包括尿白蛋白排泄。2型糖尿病患者中经常观察到尿白蛋白排泄水平高于正常。中度升高的蛋白尿水平,即所谓的微量白蛋白尿,可预测糖尿病肾病导致的肾功能进行性丧失以及心血管疾病发病率和死亡率:蛋白尿水平越高,发生肾脏和心血管并发症的可能性越大。在糖尿病肾病状态的患者中可观察到更严重的蛋白尿水平(显性蛋白尿)。在这种情况下,肾脏和心血管风险极高,并且同样可以观察到白蛋白排泄水平可预测肾脏和心血管结局。几种药物策略可降低2型糖尿病患者的尿白蛋白排泄水平。关于使用干预肾素-血管紧张素-醛固酮系统(RAAS)的药物的数据最为广泛且确凿。RAAS干预是一种非常有效的策略,可减少尿中白蛋白的量,这与治疗的降压特性无关。RAAS干预与长期肾脏和心血管保护相关。重要的是,短期内蛋白尿减少的程度与肾脏和心血管保护程度相关:蛋白尿减少越多,保护作用越强。RAAS干预的蛋白尿效应的保护预测能力与这些药物的降压效应无关(或不相关)。RAAS干预的保护作用在正常白蛋白尿、微量白蛋白尿和显性白蛋白尿水平均存在。这使得蛋白尿成为2型糖尿病的治疗靶点。目前正在测试不影响其他危险因素而降低或预防蛋白尿的新药策略,这不仅将进一步强调将蛋白尿作为一个单独靶点进行治疗的必要性,还将有助于减轻个体糖尿病患者巨大的残余风险负担。

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