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专注于肾脏疾病的钠-葡萄糖共转运蛋白 2 抑制剂结局试验:来自 CREDENCE 试验的经验教训和对 DAPA-HF、DAPA-CKD 和 EMPA-KIDNEY 试验的期望。

Dedicated kidney disease-focused outcome trials with sodium-glucose cotransporter-2 inhibitors: Lessons from CREDENCE and expectations from DAPA-HF, DAPA-CKD, and EMPA-KIDNEY.

机构信息

Division of Nephrology, Department of Medicine, Stanford University School of Medicine, Stanford, California, United States.

Stanford Diabetes Research Center, Stanford University School of Medicine, Stanford, California, United States.

出版信息

Diabetes Obes Metab. 2020 Apr;22 Suppl 1(Suppl 1):46-54. doi: 10.1111/dom.13987.

Abstract

In the past decade, many cardiovascular outcome trials (CVOT) on the efficacy and safety of glucose-lowering agents have been completed. Amongst newer agents available for treatment of type 2 diabetes mellitus (T2DM), sodium-glucose cotransporter-2 (SGLT2) inhibitors have garnered much attention in contemporary clinical practice due to observed benefits on cardiovascular and kidney outcomes among patients with T2DM, as reported in large randomized controlled trials (RCT). These findings are reflected in the updated clinical guidelines of several major professional societies. Herein, we briefly review the mechanism of action of SGLT2 inhibitors and their pleiotropic effects, summarize key findings and limitations of initial CVOTs, then discuss three major kidney disease-focused outcome trials, including the Canagliflozin and Renal Events in Diabetes and Established Nephropathy Clinical Evaluation (CREDENCE) trial as well as two ongoing RCTs: Dapagliflozin and Prevention of Adverse Outcomes in Heart Failure-chronic kidney disease and EMPA-KIDNEY.

摘要

在过去的十年中,已经完成了许多关于降低血糖药物疗效和安全性的心血管结局试验 (CVOT)。在治疗 2 型糖尿病 (T2DM) 的新型药物中,钠-葡萄糖共转运蛋白 2 (SGLT2) 抑制剂因其在 T2DM 患者中的心血管和肾脏结局方面的益处而在当代临床实践中引起了广泛关注,这在大型随机对照试验 (RCT) 中得到了证实。这些发现反映在几个主要专业协会的更新临床指南中。本文简要回顾了 SGLT2 抑制剂的作用机制及其多效性作用,总结了最初 CVOT 的关键发现和局限性,然后讨论了三项主要的以肾脏疾病为重点的结局试验,包括卡格列净和糖尿病及已确立的肾脏疾病的心血管结局事件评估 (CREDENCE) 试验以及两项正在进行的 RCT:达格列净和心力衰竭-慢性肾脏病和 EMPA-KIDNEY 预防不良结局。

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