Department of Medicine, Division of Nephrology, College of Medicine, King Saud University, Riyadh, Saudi Arabia; Division of Nephrology, University of Toronto, Toronto, ON, Canada; Division of Nephrology, Toronto General Hospital, University Health Network, Toronto, ON, Canada.
Division of Nephrology, University of Toronto, Toronto, ON, Canada; Division of Nephrology, Toronto General Hospital, University Health Network, Toronto, ON, Canada.
Am J Kidney Dis. 2023 Dec;82(6):737-742. doi: 10.1053/j.ajkd.2023.04.015. Epub 2023 Jul 29.
Concerns about hyperkalemia may result in the underuse of established and novel therapies that improve kidney and/or cardiovascular (CV) outcomes in patients with type 2 diabetes mellitus (T2DM) and chronic kidney disease (CKD). Hyperkalemia-related issues are of particular relevance in patients with CKD, who are commonly receiving other hyperkalemia-inducing agents such as renin-angiotensin-aldosterone system inhibitors and nonsteroidal mineralocorticoid receptor antagonists. In contrast, sodium/glucose transporter 2 (SGLT2) inhibitors mitigate the risk of serious hyperkalemia in clinical trials. We aim to review recent evidence surrounding the risk of hyperkalemia in patients with T2DM and CKD treated with established and novel therapies for diabetic kidney disease, focusing on SGLT2 inhibitors and nonsteroidal mineralocorticoid receptor antagonists. We conclude that SGLT2 inhibitors can be used safely in patients with T2DM at high CV risk with CKD without increasing the risk of hyperkalemia. Routine potassium monitoring is generally required when finerenone is used as a kidney- and CV-protective agent in patients with T2DM. Based on existing data, when added to the standard of care, combining SGLT2 inhibitors with finerenone is safe and has the potential to exert additional cardiorenal benefits in patients with diabetic kidney disease. The use of potassium binders should be considered to enable optimal doses of guideline-based therapies for patients with diabetic kidney disease to maximize the kidney and CV benefits.
对高钾血症的担忧可能导致 2 型糖尿病(T2DM)和慢性肾脏病(CKD)患者中已确立和新型改善肾脏和/或心血管(CV)结局的治疗方案应用不足。高钾血症相关问题在 CKD 患者中尤为重要,他们通常同时接受其他引起高钾血症的药物,如肾素-血管紧张素-醛固酮系统抑制剂和非甾体类盐皮质激素受体拮抗剂。相比之下,钠/葡萄糖共转运蛋白 2(SGLT2)抑制剂在临床试验中降低了严重高钾血症的风险。我们旨在回顾近期有关 T2DM 和 CKD 患者接受糖尿病肾病治疗方案的高钾血症风险的证据,重点关注 SGLT2 抑制剂和非甾体类盐皮质激素受体拮抗剂。我们的结论是,SGLT2 抑制剂可安全用于伴有 CKD 的高 CV 风险 T2DM 患者,不会增加高钾血症风险。当在 T2DM 患者中作为肾脏和 CV 保护剂使用非奈利酮时,通常需要常规监测血钾。基于现有数据,当将 SGLT2 抑制剂与非奈利酮联合应用于标准治疗时,其在糖尿病肾病患者中是安全的,并且有可能发挥额外的心脏肾脏获益。应考虑使用钾结合剂,以使糖尿病肾病患者能够接受最佳剂量的基于指南的治疗,从而最大程度地提高肾脏和 CV 获益。