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在心力衰竭患者中,SGLT2 抑制时水的保留超过渗透利尿。

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

机构信息

Programme in Cardiovascular and Metabolic Disorders, Duke-NUS Medical School, Singapore; Department of Internal Medicine 4-Nephrology and Hypertension, Paracelsus Private Medical School Nuremberg, Nuremberg, Germany.

Centre for Quantitative Medicine, Duke-NUS Medical School, Singapore.

出版信息

J Am Coll Cardiol. 2024 Apr 16;83(15):1386-1398. doi: 10.1016/j.jacc.2024.02.020.

Abstract

BACKGROUND

Sodium-glucose cotransporter 2 inhibitors are believed to improve cardiac outcomes due to their osmotic diuretic potential.

OBJECTIVES

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.

METHODS

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.

RESULTS

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).

CONCLUSIONS

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).

摘要

背景

钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)被认为通过其渗透利尿潜能改善心脏结局。

目的

本研究旨在检验以下假设,即血管加压素驱动的尿液浓缩作用超过了达格列净治疗引起的葡萄糖尿的渗透利尿作用。

方法

DAPA-Shuttle1(心力衰竭患者 SGLT-2i 治疗的肝-肾水合作用调控)是一项单中心、双盲、随机、安慰剂对照试验,纳入慢性心力衰竭 NYHA 心功能 I/II 级和射血分数降低的患者,随机接受每日 10mg 达格列净或安慰剂(1:1)治疗 4 周。主要终点是与基线相比尿液渗透溶质浓度的变化。次要终点包括 copeptin 水平和溶质自由水清除率的变化。

结果

33 名随机、钠-葡萄糖共转运蛋白 2 抑制剂初治参与者完成了研究,其中 29 名(安慰剂:n=14;达格列净:n=15)提供了准确的 24 小时尿液收集(平均年龄 59±14 岁;左心室射血分数 31%±9%)。达格列净治疗在 48 小时(早期)内导致尿葡萄糖排泄增加 3.3mmol/kg/d(95%CI:2.51-4.04;P<0.0001),并在 4 周后持续存在(晚期;2.7mmol/kg/d [95%CI:1.98-3.51];P<0.0001)。达格列净治疗早期(5.5pmol/L [95%CI:0.45-10.5];P<0.05)和晚期(7.8pmol/L [95%CI:2.77-12.81];P<0.01)血清 copeptin 增加,导致自由水清除率呈比例下降(早期:-9.1mL/kg/d [95%CI:-14 至-4.12;P<0.001];晚期:-11.0mL/kg/d [95%CI:-15.94 至-6.07;P<0.0001])和尿液浓度升高(晚期:134mmol/L [95%CI:39.28-229.12];P<0.01)。因此,达格列净治疗并没有显著增加尿容量(早期平均差异:2.8mL/kg/d [95%CI:-1.97 至 7.48;P=0.25];晚期平均差异:0.9mL/kg/d [95%CI:-3.83 至 5.62];P=0.70)。

结论

生理适应性水合作用消除了达格列净预期的渗透利尿潜能,从而阻止了约 10mL/kg/d·75kg=750mL/kg/d 的葡萄糖驱动的尿容量增加。(心力衰竭患者 SGLT-2i 治疗的肝-肾水合作用调控 [DAPA-Shuttle1];NCT04080518)。

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