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预防终末期肾病。

Preventing end-stage renal disease.

作者信息

Mogensen C E

机构信息

Department of Diabetes and Endocrinology, Aarhus Kommunehospital, Denmark.

出版信息

Diabet Med. 1998;15 Suppl 4:S51-6. doi: 10.1002/(SICI)1096-9136(1998120)15:4+<S51::AID-DIA740>3.0.CO;2-Y.

Abstract

Interest in evidence-based medicine is increasing greatly, with the focus on treatment that prevents organ failure and that may prolong life. Type 1 and Type 2 diabetes are conditions associated with increased mortality, mainly as a result of renal and cardiovascular diseases, and blindness. All three complications usually occur together. In recent years, more focus has been placed on treating patients early to prevent future organ damage. Microalbuminuria is an important intermediary end-point that correlates strongly with future advanced renal disease, retinopathy and mortality. Several trials have studied patients with microalbuminuria and also patients in more advanced stages of the disease who have proteinuria (termed overt nephropathy). Recent evidence indicates that achieving optimal glycaemic control reduces the risk of an increase in urinary albumin excretion before the development of microalbuminuria. Angiotensin-converting enzyme (ACE) inhibitors are effective in reducing microalbuminuria, partly independent of their blood pressure reducing effects. In Type 1 and Type 2 diabetic patients with microalbuminuria, long-term treatment with ACE inhibitors (7-8 years) prevents the predicted decrease in glomerular filtration rate (GFR); optimal glycaemic control is also important in preventing the decline in GFR. This is important because GFR is usually well preserved in Type 1 and Type 2 diabetic patients with microalbuminuria and a predicted decline in GFR can therefore be prevented. In overt renal disease, studies that focused mostly on Type 1 diabetic patients have shown that the rate of decline in GFR can be reduced. Long-term studies in Type 1 diabetic patients have also demonstrated that mortality caused by end-stage renal disease can be postponed. Mortality associated with cardiovascular diseases, e.g. myocardial infarction, is reduced more effectively in diabetic patients treated with ACE inhibitors and beta-blockers than in non-diabetic patients treated with the same drugs. Screening for microalbuminuria, the attainment of optimal glycaemic control, and early treatment with ACE inhibitors and other antihypertensive drugs are necessary to prevent progression of diabetic complications, especially diabetic nephropathy. However, there is some controversy about the initial use of calcium channel blockers. In conclusion, early achievement of improved glycaemic control is the most important factor in the prevention of diabetic complications. Antihypertensive treatment is clearly also important.

摘要

对循证医学的关注正在大幅增加,重点在于预防器官衰竭和延长生命的治疗方法。1型和2型糖尿病与死亡率增加相关,主要是由于肾脏和心血管疾病以及失明。这三种并发症通常同时出现。近年来,更多的重点放在早期治疗患者以预防未来的器官损害。微量白蛋白尿是一个重要的中间终点,与未来的晚期肾病、视网膜病变和死亡率密切相关。多项试验研究了微量白蛋白尿患者以及疾病更晚期出现蛋白尿(称为显性肾病)的患者。最近的证据表明,实现最佳血糖控制可降低微量白蛋白尿发生前尿白蛋白排泄增加的风险。血管紧张素转换酶(ACE)抑制剂在减少微量白蛋白尿方面有效,部分独立于其降压作用。在患有微量白蛋白尿的1型和2型糖尿病患者中,长期使用ACE抑制剂(7 - 8年)可预防肾小球滤过率(GFR)的预期下降;最佳血糖控制对于预防GFR下降也很重要。这很重要,因为在患有微量白蛋白尿的1型和2型糖尿病患者中,GFR通常保存良好,因此可以预防GFR的预期下降。在显性肾病中,主要针对1型糖尿病患者的研究表明,GFR的下降速率可以降低。对1型糖尿病患者的长期研究还表明,终末期肾病导致的死亡率可以推迟。与心血管疾病(如心肌梗死)相关的死亡率,在使用ACE抑制剂和β受体阻滞剂治疗的糖尿病患者中比使用相同药物治疗的非糖尿病患者中降低得更有效。筛查微量白蛋白尿、实现最佳血糖控制以及早期使用ACE抑制剂和其他抗高血压药物对于预防糖尿病并发症,尤其是糖尿病肾病的进展是必要的。然而,关于钙通道阻滞剂的初始使用存在一些争议。总之,早期实现更好的血糖控制是预防糖尿病并发症的最重要因素。抗高血压治疗显然也很重要。

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