Prescribing SGLT2 Inhibitors in Patients With CKD: Expanding Indications and Practical Considerations

被引:134
作者
Yau, Kevin [1 ,2 ]
Dharia, Atit [1 ,2 ]
Alrowiyti, Ibrahim [1 ,2 ]
Cherney, David Z. I. [1 ,2 ,3 ]
机构
[1] Univ Hlth Network, Dept Med, Div Nephrol, Toronto, ON, Canada
[2] Univ Toronto, Dept Med, Toronto, ON, Canada
[3] Toronto Gen Hosp, Dept Med, Div Nephrol, 585 Univ Ave,8N-845, Toronto, ON M5G 2N2, Canada
基金
加拿大健康研究院;
关键词
chronic kidney disease; diabetes; diabetic kidney disease; glomerulonephritis; heart failure; SGLT2; inhibitors; COTRANSPORTER; 2; INHIBITORS; TYPE-2; DIABETES-MELLITUS; CHRONIC KIDNEY-DISEASE; DOUBLE-BLIND; DAPAGLIFLOZIN; OUTCOMES; SAFETY; RISK; EMPAGLIFLOZIN; EFFICACY;
D O I
10.1016/j.ekir.2022.04.094
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
SGLT2 inhibitors have emerged as a key disease-modifying therapy to prevent the progression of chronic kidney disease (CKD). These agents prevent decline in kidney function through reduction in glomerular hypertension mediated through tubuloglomerular feedback independent of their effect on glycemic con-trol. The proliferation of clinical trials on SGLT2 inhibitors has rapidly expanded the approved clinical indications for these agents beyond patients with diabetes mellitus (DM). We review the current in-dications for SGLT2 inhibitors in patients with and without diabetic kidney disease, including new evidence for use in patients with heart failure with or without reduced ejection fraction, stage 4 CKD, and chronic glomerulonephritis. The EMPA-KIDNEY trial was recently stopped early for efficacy suggesting that SGLT2 inhibitors may soon be indicated for patients with CKD without albuminuria. We review practical con-siderations for prescription of SGLT2 inhibitors, including the anticipated acute decline in estimated glomerular filtration rate (eGFR) on initiation, initiating the lowest dosage used in clinical trials, volume status considerations, and adverse event mitigation. Combination therapy in patients with DM may be considered with agents, including glucagon-like peptide-1 receptor agonists (GLP-1-RAs), novel mineral-ocorticoid receptor antagonists, and selective endothelin receptor antagonists to reduce residual albu-minuria and cardiovascular risk. Kidney Int Rep (2022) 7, 1463-1476; https://doi.org/10.1016/j.ekir.2022.04.094
引用
收藏
页码:1463 / 1476
页数:14
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