Water Conservation Overrides Osmotic Diuresis During SGLT2 Inhibition in Patients With Heart Failure

达帕格列嗪 医学 安慰剂 射血分数 心力衰竭 利尿剂 自由水间隙 内科学 尿渗透压 内分泌学 利尿 Copeptin蛋白 临床终点 排泄 泌尿科 随机对照试验 肾功能 糖尿病 加压素 2型糖尿病 病理 替代医学
作者
Adriana Marton,Seyed Ehsan Saffari,Manfred Rauh,Ruo-Ning Sun,Armin M. Nagel,Peter Linz,Tzy Tiing Lim,Kaoru Takase-Minegishi,Anastacia Pajarillaga,Sharon Saw,Norihiko Morisawa,Wan Keat Yam,Shintaro Minegishi,John J. Totman,Serena Teo,Louis Teo,Choon Ta Ng,Kento Kitada,Johannes Wild,Jean‐Paul Kovalik,Friedrich C. Luft,Peter J. Greasley,Calvin Chin,David K.L. Sim,Jens Titze
出处
期刊:Journal of the American College of Cardiology [Elsevier BV]
卷期号:83 (15): 1386-1398 被引量:10
标识
DOI:10.1016/j.jacc.2024.02.020
摘要

Sodium-glucose cotransporter 2 inhibitors are believed to improve cardiac outcomes due to their osmotic diuretic potential. The goal of this study was to test the hypothesis that vasopressin-driven urine concentration overrides the osmotic diuretic effect of glucosuria induced by dapagliflozin treatment. DAPA-Shuttle1 (Hepato-renal Regulation of Water Conservation in Heart Failure Patients With SGLT-2 Inhibitor Treatment) was a single-center, double-blind, randomized, placebo-controlled trial, in which patients with chronic heart failure NYHA functional classes I/II and reduced ejection fraction were randomly assigned to receive dapagliflozin 10 mg daily or placebo (1:1) for 4 weeks. The primary endpoint was change from baseline in urine osmolyte concentration. Secondary endpoints included changes in copeptin levels and solute free water clearance. Thirty-three randomized, sodium-glucose cotransporter 2 inhibitor–naïve participants completed the study, 29 of whom (placebo: n = 14; dapagliflozin: n = 15) provided accurate 24-hour urine collections (mean age 59 ± 14 years; left ventricular ejection fraction 31% ± 9%). Dapagliflozin treatment led to an isolated increase in urine glucose excretion by 3.3 mmol/kg/d (95% CI: 2.51–4.04; P < 0.0001) within 48 hours (early) which persisted after 4 weeks (late; 2.7 mmol/kg/d [95% CI: 1.98–3.51]; P < 0.0001). Dapagliflozin treatment increased serum copeptin early (5.5 pmol/L [95% CI: 0.45-10.5]; P < 0.05) and late (7.8 pmol/L [95% CI: 2.77–12.81]; P < 0.01), leading to proportional reductions in free water clearance (early: −9.1 mL/kg/d [95% CI: −14 to −4.12; P < 0.001]; late: −11.0 mL/kg/d [95% CI: −15.94 to −6.07; P < 0.0001]) and elevated urine concentrations (late: 134 mmol/L [95% CI: 39.28–229.12]; P < 0.01). Therefore, urine volume did not significantly increase with dapagliflozin (mean difference early: 2.8 mL/kg/d [95% CI: −1.97 to 7.48; P = 0.25]; mean difference late: 0.9 mL/kg/d [95% CI: −3.83 to 5.62]; P = 0.70). Physiological-adaptive water conservation eliminated the expected osmotic diuretic potential of dapagliflozin and thereby prevented a glucose-driven increase in urine volume of approximately 10 mL/kg/d · 75 kg = 750 mL/kg/d. (Hepato-renal Regulation of Water Conservation in Heart Failure Patients With SGLT-2 Inhibitor Treatment [DAPA-Shuttle1]; NCT04080518).
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