Podestà Manuel Alfredo, Sabiu Gianmarco, Galassi Andrea, Ciceri Paola, Cozzolino Mario
Renal Division, ASST Santi Paolo e Carlo, Department of Health Sciences, Università degli Studi di Milano, 20154 Milano, Italy.
Transplantation Research Center, Renal Division, Harvard Medical School, Brigham and Women's Hospital, Boston, MA 02115, USA.
Biomedicines. 2023 Jan 19;11(2):279. doi: 10.3390/biomedicines11020279.
Results from recent randomized controlled trials on inhibitors of the sodium-glucose cotransporter 2 (SGLT2) have determined a paradigm shift in the treatment of patients with type 2 diabetes mellitus. These agents have been shown not only to ameliorate metabolic control, but also to independently protect from cardiovascular events and to reduce the progression of chronic kidney disease (CKD) in these patients. The magnitude of the nephroprotective effect observed in these studies is likely to make SGLT2 inhibitors the most impactful drug class for the treatment of diabetic patients with CKD since the discovery of renin-angiotensin system inhibitors. Even more surprisingly, SGLT2 inhibitors have also been shown to slow CKD progression in non-diabetic individuals with varying degrees of proteinuria, suggesting that activation of SGLT2 is involved in the pathogenesis of CKD independent of its etiology. As indications continue to expand, it is still unclear whether the observed benefits of SGLT2 inhibitors may extend to CKD patients at lower risk of progression and if their association with other agents may confer additional protection.
近期关于钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂的随机对照试验结果,已确定了2型糖尿病患者治疗模式的转变。这些药物不仅已被证明可改善代谢控制,还能独立预防心血管事件,并减缓这些患者慢性肾脏病(CKD)的进展。在这些研究中观察到的肾脏保护作用程度,可能使SGLT2抑制剂成为自肾素-血管紧张素系统抑制剂发现以来,对糖尿病合并CKD患者治疗影响最大的药物类别。更令人惊讶的是,SGLT2抑制剂还被证明可减缓不同程度蛋白尿的非糖尿病个体的CKD进展,这表明SGLT2的激活参与了CKD的发病机制,与其病因无关。随着适应证不断扩大,目前仍不清楚SGLT2抑制剂观察到的益处是否可能扩展至进展风险较低的CKD患者,以及它们与其他药物联合使用是否可能带来额外保护。