Persson Frederik, Borg Rikke, Rossing Peter
Steno Diabetes Center Copenhagen, Denmark.
Zealand University Hospital Roskilde, Denmark.
Ann Transl Med. 2021 Apr;9(8):716. doi: 10.21037/atm-20-4841.
Diabetic kidney disease is a frequent and costly complication to type 2 diabetes. After many years with a lack of successful trials there are now significant developments that will change treatment, guidelines and future outcome. Since the last two decades blockade of the renin-angiotensin system (RAS) is standard treatment, but new antidiabetic treatments have shown potential for kidney protection. After cardiovascular outcome studies with glucagon-like peptide (GLP-1) receptor agonists it is evident that drugs like liraglutide, semaglutide and dulaglutide can reduce albuminuria levels and progression to macroalbuminuria. At present, a renal outcome trial with semaglutide is ongoing which will provide more evidence on the drug class in the future. The sodium glucose co-transporter 2 (SGLT2) inhibitor class has also demonstrated effects beyond glucose-lowering, as the drugs can reduce blood pressure, albuminuria and loss of renal function. In the first renal outcome study the SGLT2 inhibitor canagliflozin was found to reduce the risk of hard renal outcome with 30%. SGLT2 inhibition is now recommended in type 2 diabetes with chronic kidney disease. Renal outcome studies testing additional SGLT2 inhibitors and the GLP-1 receptor agonist semaglutide will report in the coming future potentially providing more and much needed options for treatment.
糖尿病肾病是2型糖尿病常见且代价高昂的并发症。在多年缺乏成功试验之后,现在有了重大进展,这将改变治疗方法、指南和未来的治疗结果。在过去二十年中,肾素-血管紧张素系统(RAS)阻滞剂一直是标准治疗方法,但新的抗糖尿病治疗方法已显示出肾脏保护潜力。在使用胰高血糖素样肽(GLP-1)受体激动剂进行心血管结局研究后,很明显,利拉鲁肽、司美格鲁肽和度拉鲁肽等药物可以降低蛋白尿水平并延缓进展为大量蛋白尿。目前,一项关于司美格鲁肽的肾脏结局试验正在进行,这将在未来为该药物类别提供更多证据。钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂类药物也已证明具有降糖以外的作用,因为这些药物可以降低血压、蛋白尿和肾功能丧失。在第一项肾脏结局研究中,发现SGLT2抑制剂卡格列净可将严重肾脏结局的风险降低30%。目前,SGLT2抑制已被推荐用于患有慢性肾病的2型糖尿病患者。测试其他SGLT2抑制剂和GLP-1受体激动剂司美格鲁肽的肾脏结局研究将在未来公布,可能会提供更多且急需的治疗选择。