Department of Nephrology, Osaka University Graduate School of Medicine, 2-2-D11, Yamada-oka, Suita, Osaka, 565-0871, Japan.
Department of Cardiology, Pulmonology, Hypertension and Nephrology, Ehime University Graduate School of Medicine, Toon, Ehime, Japan.
Clin Exp Nephrol. 2024 Jul;28(7):629-635. doi: 10.1007/s10157-024-02467-w. Epub 2024 Feb 25.
Volume overload is common and associated with high mortality in patients on peritoneal dialysis (PD). Traditional strategies including diuretics, water/salt restriction, and icodextrin-based solutions cannot always fully correct this condition, necessitating novel alternative strategies. Recent studies confirmed the expression of sodium-glucose cotransporter 2 (SGLT2) in the human peritoneum. Experimental data suggest that SGLT2 inhibitors decrease glucose absorption from the PD solution, thereby increasing the ultrafiltration volume. This trial aims to assess whether SGLT2 inhibitors increase the ultrafiltration volume in patients on PD.
The EMPOWERED trial (trial registration: jRCTs051230081) is a multicenter, randomized, double-blind, placebo-controlled, crossover trial. Patients with clinically diagnosed chronic heart failure are eligible regardless of the presence of diabetes if they use at least 3 L/day glucose-based PD solutions. Participants will be randomly assigned (1:1) to receive empagliflozin 10 mg once daily and then placebo or vice versa. Each treatment period will last 8 weeks with a 4-week washout period. This study will recruit at least 36 randomized participants. The primary endpoint is the change in the daily ultrafiltration volume from baseline to week 8 in each intervention period. The key secondary endpoints include changes in the biomarkers of drained PD solutions, renal residual function, and anemia-related parameters.
This trial aims to assess the benefit of SGLT2 inhibitors in fluid management with a novel mechanism of action in patients on PD. It will also provide insights into the effects of SGLT2 inhibitors on solute transport across the peritoneal membrane and residual renal function.
容量超负荷在腹膜透析(PD)患者中很常见,且与高死亡率相关。传统策略,包括利尿剂、水/盐限制和基于艾考糊精的溶液,并不总能完全纠正这种情况,因此需要新的替代策略。最近的研究证实了钠-葡萄糖共转运蛋白 2(SGLT2)在人腹膜中的表达。实验数据表明,SGLT2 抑制剂可减少 PD 溶液中葡萄糖的吸收,从而增加超滤量。本试验旨在评估 SGLT2 抑制剂是否可增加 PD 患者的超滤量。
EMPOWERED 试验(试验注册:jRCTs051230081)是一项多中心、随机、双盲、安慰剂对照、交叉试验。患有临床诊断的慢性心力衰竭的患者,如果使用至少 3 L/天的基于葡萄糖的 PD 溶液,则无论是否存在糖尿病,均符合入选条件。参与者将被随机分配(1:1)接受恩格列净 10 mg 每日一次,然后接受安慰剂或反之亦然。每个治疗期持续 8 周,洗脱期为 4 周。本研究将招募至少 36 名随机参与者。主要终点是每个干预期内从基线到第 8 周的每日超滤量变化。主要次要终点包括从基线到第 8 周引流 PD 溶液中生物标志物、残余肾功能和与贫血相关参数的变化。
本试验旨在评估 SGLT2 抑制剂在 PD 患者液体管理中的获益,其作用机制新颖。它还将提供关于 SGLT2 抑制剂对跨腹膜溶质转运和残余肾功能影响的见解。