Wever Britt Eveline, Scholtes Rosalie Annemien, Mosterd Charlotte Michelle, Hesp Anne Clasien, Smits Mark Martinus, Heerspink Hiddo Jan Lambers, van Raalte Daniël Henri
Diabetes Center, Department of Internal Medicine, Amsterdam University Medical Centers, Location VUMC, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands.
Department of Clinical Pharmacy and Pharmacology, University Medical Center Groningen, Groningen, The Netherlands.
J Nephrol. 2025 Apr 12. doi: 10.1007/s40620-025-02289-3.
Renin-angiotensin system inhibitors (RASi) and sodium glucose cotransporter inhibitors (SGLT2i) are known for their kidney protective properties, but both show significant residual risk in large outcome trials. In these trials, SGLT2i were introduced on top of RASi; the individual response to each drug is currently unclear. We therefore aimed to investigate the individual reactions to the angiotensin II receptor blocker (ARB) losartan and the SGLT2i empagliflozin and their combination on measured GFR (mGFR) and systolic blood pressure (SBP).
In this double-blind, randomized, 4-armed, crossover study, 24 participants received 7 days of empagliflozin 10 mg once daily, losartan 50 mg once daily, combination therapy or matching placebo. We visualized individual drug response variability. We further explored predictors of mGFR and SBP changes.
During empagliflozin administration, a greater than 10% reduction in mGFR was observed in 26% of participants receiving empagliflozin, in 30% of those receiving losartan, and in 39% among participants on combination therapy. In comparison, a greater than 10% reduction in SBP was observed in 35% of participants on empagliflozin, in 39% of those receiving losartan and in 43% on combination therapy. A large part of the participants who did not respond to one drug, did respond to the other drug or their combination. Monotherapy SGLT2i did not correlate with monotherapy ARB in mGFR change or SBP change.
Our data show large individual variability in response to treatment with the ARB losartan and the SGLT2i empagliflozin. Clinicians should monitor treatment responses in patients and consider switching from one kidney protective drug to another in non-responders.
肾素-血管紧张素系统抑制剂(RASi)和钠-葡萄糖协同转运蛋白抑制剂(SGLT2i)以其肾脏保护特性而闻名,但在大型结局试验中两者均显示出显著的残余风险。在这些试验中,SGLT2i是在RASi基础上加用的;目前尚不清楚个体对每种药物的反应。因此,我们旨在研究血管紧张素II受体阻滞剂(ARB)氯沙坦、SGLT2i恩格列净及其联合用药对测量的肾小球滤过率(mGFR)和收缩压(SBP)的个体反应。
在这项双盲、随机、四臂、交叉研究中,24名参与者接受了为期7天的每日一次10mg恩格列净、每日一次50mg氯沙坦、联合治疗或匹配安慰剂。我们直观展示了个体药物反应变异性。我们进一步探索了mGFR和SBP变化的预测因素。
在服用恩格列净期间,接受恩格列净治疗的参与者中有26%、接受氯沙坦治疗的参与者中有30%以及接受联合治疗的参与者中有39%的mGFR降低超过10%。相比之下,接受恩格列净治疗的参与者中有35%、接受氯沙坦治疗的参与者中有39%以及接受联合治疗的参与者中有43%的SBP降低超过10%。很大一部分对一种药物无反应的参与者对另一种药物或其联合用药有反应。单药治疗SGLT2i与单药治疗ARB在mGFR变化或SBP变化方面无相关性。
我们的数据显示,对ARB氯沙坦和SGLT2i恩格列净治疗的反应存在很大的个体变异性。临床医生应监测患者的治疗反应,并考虑在无反应者中从一种肾脏保护药物转换为另一种。