Caravaca-Fontán Fernando, Del Vecchio Lucia, Praga Manuel, Floege Jürgen, Zoccali Carmine
Department of Nephrology, Instituto de Investigación Hospital 12 de Octubre (imas12), Madrid, Spain.
Department of Nephrology and Dialysis, ASST Lariana, Como, Italy.
Clin Kidney J. 2024 Aug 12;17(9):sfae237. doi: 10.1093/ckj/sfae237. eCollection 2024 Sep.
Integrating sodium-glucose co-transporter 2 inhibitors (SGLT2i) into the treatment for chronic kidney disease (CKD) has marked a significant therapeutic advance in nephrology. Clinical trials such as DAPA-CKD and EMPA-KIDNEY have demonstrated the beneficial effects of SGLT2i in slowing CKD progression and reducing proteinuria. However, the applicability of these results to patients with glomerulonephritis is still unresolved due to various limitations. This manuscript combines the evidence supporting the use of SGLT2i in glomerular diseases, highlights the limitations and strikes a conclusive balance on their role in clinical practice.
将钠-葡萄糖协同转运蛋白2抑制剂(SGLT2i)纳入慢性肾脏病(CKD)治疗已标志着肾脏病学领域的一项重大治疗进展。诸如DAPA-CKD和EMPA-KIDNEY等临床试验已证明SGLT2i在延缓CKD进展和减少蛋白尿方面的有益作用。然而,由于各种局限性,这些结果在肾小球肾炎患者中的适用性仍未得到解决。本手稿综合了支持在肾小球疾病中使用SGLT2i的证据,强调了局限性,并就其在临床实践中的作用达成了结论性的平衡。