Toto Robert D
University of Texas Southwestern Medical Center at Dallas, Department of Medicine, 5323 Harry Hines Boulevard, Dallas, TX 75390-8856, USA.
Curr Diab Rep. 2002 Dec;2(6):545-52. doi: 10.1007/s11892-002-0126-y.
Diabetic nephropathy is the leading cause of end-stage kidney disease in the United States. The majority of these cases are attributed to those with type 2 diabetes. Elevated blood pressure, proteinuria, and increased activity of the renin-angiotensin-aldosterone system (RAAS) play a major role in the development and progression of chronic kidney disease attributed to diabetes mellitus. Moreover, drugs that inhibit angiotensin II synthesis or block the angiotensin II type I receptor lower blood pressure, reduce proteinuria, and improve outcomes in patients with chronic kidney disease caused by diabetes. This article highlights improvements in the current management of diabetic nephropathy afforded by agents that inhibit the RAAS, discusses their limitations, and considers novel strategies to prevent onset and progression of diabetic nephropathy. Current opinions concerning combination drug therapy with agents that block the RAAS at multiple sites, as well as combining calcium channel blockers with either angiotensin-converting enzyme inhibitors or angiotensin II receptor antagonists, are also discussed.
糖尿病肾病是美国终末期肾病的主要病因。这些病例大多归因于2型糖尿病患者。血压升高、蛋白尿以及肾素-血管紧张素-醛固酮系统(RAAS)活性增加在糖尿病所致慢性肾脏病的发生和发展中起主要作用。此外,抑制血管紧张素II合成或阻断血管紧张素II 1型受体的药物可降低血压、减少蛋白尿,并改善糖尿病所致慢性肾脏病患者的预后。本文重点介绍了抑制RAAS的药物在糖尿病肾病当前治疗中的进展,讨论了它们的局限性,并探讨了预防糖尿病肾病发生和进展的新策略。还讨论了关于使用在多个位点阻断RAAS的药物进行联合药物治疗,以及将钙通道阻滞剂与血管紧张素转换酶抑制剂或血管紧张素II受体拮抗剂联合使用的当前观点。