Berbari Adel E
Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
Int J Cardiol Hypertens. 2020 Oct 20;7:100058. doi: 10.1016/j.ijchy.2020.100058. eCollection 2020 Dec.
Diabetic kidney disease (diabetic nephropathy), one of the most serious renovascular diabetic complication represents the leading cause of chronic kidney disease worldwide and is characterized clinically by impaired renal functional indices, hypertension, systemic and renal hemodynamic changes and pathologically by a spectrum of glomerulotubulointerstitial and vascular lesions. Diabetic nephropathy is initiated by persistent hyperglycemia and glomerular hyperfiltration and, if untreated, progresses to increasing albuminuria, declining glomerular filtration rate (GFR), development of end-stage renal failure (ESRF) and or enhanced risk of poor cardiovascular outcomes. The emergence of sodium glucose co-transporter 2 (SGLT2) inhibitors, a novel class of antidiabetic drugs endowed with a wide range of pleiotropic actions revolutionized care of diabetes and its complications. These drugs reduce major cardiovascular events, heart failure hospitalization, rate of progression of albuminuria, and decline in GFR in both diabetic and non-diabetic patients with preserved or impaired renal function and development of ESRF.
糖尿病肾病是最严重的糖尿病血管并发症之一,是全球慢性肾脏病的主要病因,临床特征为肾功能指标受损、高血压、全身和肾脏血流动力学改变,病理特征为一系列肾小球、肾小管间质和血管病变。糖尿病肾病由持续性高血糖和肾小球高滤过引发,若不治疗,会进展为蛋白尿增加、肾小球滤过率(GFR)下降、终末期肾衰竭(ESRF),和/或心血管不良结局风险增加。钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂的出现,这是一类具有多种多效性作用的新型抗糖尿病药物,彻底改变了糖尿病及其并发症的治疗。这些药物可降低糖尿病和非糖尿病患者(肾功能正常或受损以及ESRF患者)的主要心血管事件、心力衰竭住院率、蛋白尿进展率和GFR下降。