Granata Antonio, Pesce Francesco, Iacoviello Massimo, Anzaldi Massimiliano, Amico Francesco, Catalano Maria, Leonardi Giuseppe, Gatta Carmela, Costanza Giusy, Corrao Salvatore, Gesualdo Loreto
Nephrology and Dialysis Unit, "Cannizzaro" Emergency Hospital, Catania, Italy.
Renal, Dialysis and Transplantation Unit, Department of Emergency and Organ Transplantation, University of Bari, Bari, Italy.
Front Nephrol. 2022 Apr 29;2:867075. doi: 10.3389/fneph.2022.867075. eCollection 2022.
Since their introduction as antidiabetic drugs, SGLT2 inhibitors (SGLT2i) have come a long way, proving to be beneficial on cardiovascular and renal outcomes independently of diabetes status. The benefits go far beyond glycemic control, and both the cardio- and nephroprotection are underpinned by diverse mechanisms. From the activation of tubule glomerular feedback and the consequent reduction in hyperfiltration to the improvement of hypoxia and oxidative stress in the renal cortex, SGLT2i have also been shown to inhibit hepcidin and limit podocyte damage. Likewise, they improve cardiac metabolism and bioenergetics, and reduce necrosis and cardiac fibrosis and the production of adipokines, cytokines, and epicardial adipose tissue mass. In terms of outcomes, the efficacy has been demonstrated on blood pressure control, BMI, albuminuria, stroke, heart disease, and mortality rate due to cardiovascular events. Patients with chronic kidney disease and proteinuria, with or without diabetes, treated with some SGLT2i have a reduced risk of progression. The analysis of subgroups of individuals with specific diseases such as IgA nephropathy has confirmed this solid effect on renal outcomes. Given these overarching activities on such a broad pathophysiological background and the favorable safety profile that goes with the use of SGLT2i, it is now certain that they are changing our approach to clinical interventions for important outcomes with an impressive impact.
自作为抗糖尿病药物引入以来,钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)已经走过了漫长的道路,事实证明,无论糖尿病状态如何,它们对心血管和肾脏结局都有益处。其益处远不止于血糖控制,心脏保护和肾脏保护均由多种机制支撑。从激活肾小管-肾小球反馈并由此减少超滤,到改善肾皮质的缺氧和氧化应激,SGLT2i还被证明可抑制铁调素并限制足细胞损伤。同样,它们可改善心脏代谢和生物能量学,减少坏死、心脏纤维化以及脂肪因子、细胞因子和心外膜脂肪组织量的产生。在结局方面,已证实其在血压控制、体重指数、蛋白尿、中风、心脏病以及心血管事件导致的死亡率方面具有疗效。使用某些SGLT2i治疗的慢性肾脏病和蛋白尿患者,无论是否患有糖尿病,疾病进展风险均降低。对患有特定疾病(如IgA肾病)的个体亚组分析证实了其对肾脏结局的这种确切疗效。鉴于在如此广泛的病理生理背景下具有这些总体作用,以及使用SGLT2i所具有的良好安全性,现在可以确定的是,它们正在改变我们对重要结局进行临床干预的方法,并产生令人印象深刻的影响。