Department of Medicine, University of Padua, Padua, Italy
Department of Medicine, University of Padua, Padua, Italy.
Diabetes Care. 2016 Aug;39 Suppl 2:S165-71. doi: 10.2337/dcS15-3006.
Diabetic nephropathy (DN) is the most common cause of end-stage renal disease worldwide. Blood glucose and blood pressure control reduce the risk of developing this complication; however, once DN is established, it is only possible to slow progression. Sodium-glucose cotransporter 2 (SGLT2) inhibitors, the most recent glucose-lowering oral agents, may have the potential to exert nephroprotection not only through improving glycemic control but also through glucose-independent effects, such as blood pressure-lowering and direct renal effects. It is important to consider, however, that in patients with impaired renal function, given their mode of action, SGLT2 inhibitors are less effective in lowering blood glucose. In patients with high cardiovascular risk, the SGLT2 inhibitor empagliflozin lowered the rate of cardiovascular events, especially cardiovascular death, and substantially reduced important renal outcomes. Such benefits on DN could derive from effects beyond glycemia. Glomerular hyperfiltration is a potential risk factor for DN. In addition to the activation of the renin-angiotensin-aldosterone system, renal tubular factors, including SGLT2, contribute to glomerular hyperfiltration in diabetes. SGLT2 inhibitors reduce sodium reabsorption in the proximal tubule, causing, through tubuloglomerular feedback, afferent arteriole vasoconstriction and reduction in hyperfiltration. Experimental studies showed that SGLT2 inhibitors reduced hyperfiltration and decreased inflammatory and fibrotic responses of proximal tubular cells. SGLT2 inhibitors reduced glomerular hyperfiltration in patients with type 1 diabetes, and in patients with type 2 diabetes, they caused transient acute reductions in glomerular filtration rate, followed by a progressive recovery and stabilization of renal function. Interestingly, recent studies consistently demonstrated a reduction in albuminuria. Although these data are promising, only dedicated renal outcome trials will clarify whether SGLT2 inhibitors, in addition to their glycemic and blood pressure benefits, may provide nephroprotective effects.
糖尿病肾病(DN)是全球范围内导致终末期肾病的最常见原因。控制血糖和血压可以降低发生这种并发症的风险;然而,一旦 DN 确立,就只能减缓其进展。钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂是最近出现的降血糖口服药物,除了通过改善血糖控制发挥潜在的肾脏保护作用外,还可能通过降低血压和直接肾脏作用等血糖非依赖性作用发挥肾脏保护作用。然而,需要注意的是,在肾功能受损的患者中,由于其作用机制,SGLT2 抑制剂在降低血糖方面的效果较差。在心血管风险较高的患者中,SGLT2 抑制剂恩格列净降低了心血管事件的发生率,特别是心血管死亡的发生率,并显著减少了重要的肾脏结局。这些对 DN 的益处可能源自于血糖控制以外的作用。肾小球高滤过是 DN 的一个潜在危险因素。除了肾素-血管紧张素-醛固酮系统的激活外,包括 SGLT2 在内的肾小管因素也促成了糖尿病中的肾小球高滤过。SGLT2 抑制剂减少近端肾小管中的钠重吸收,通过管球反馈引起入球小动脉收缩和高滤过减少。实验研究表明,SGLT2 抑制剂可减少高滤过并降低近端肾小管细胞的炎症和纤维化反应。SGLT2 抑制剂可减少 1 型糖尿病患者的肾小球高滤过,在 2 型糖尿病患者中,它们会导致肾小球滤过率一过性急性下降,随后肾功能逐渐恢复和稳定。有趣的是,最近的研究一致表明白蛋白尿减少。尽管这些数据很有前景,但只有专门的肾脏结局试验才能明确 SGLT2 抑制剂除了具有降血糖和降压作用外,是否还能提供肾脏保护作用。