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Effects of Dapagliflozin on Volume Status When Added to Renin–Angiotensin System Inhibitors

机译:当加入肾素-血管紧张素系统抑制剂时达格列净对容量状态的影响

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摘要

Sodium glucose co-transporter 2 (SGLT2) inhibitors reduce the risk of heart and kidney failure in patients with type 2 diabetes, possibly due to diuretic effects. Previous non-placebo-controlled studies with SGLT2 inhibitors observed changes in volume markers in healthy individuals and in patients with type 2 diabetes with preserved kidney function. It is unclear whether patients with type 2 diabetes and signs of kidney damage show similar changes. Therefore, a post hoc analysis was performed on two randomized controlled trials (n = 69), assessing effects of dapagliflozin 10 mg/day when added to renin–angiotensin system inhibition in patients with type 2 diabetes and urinary albumin-to-creatinine ratio ≥30 mg/g. Blood and 24-h urine was collected at the start and the end of treatment periods lasting six and 12 weeks. Effects of dapagliflozin compared to placebo on various markers of volume status were determined. Fractional lithium excretion, a marker of proximal tubular sodium reabsorption, was assessed in 33 patients. Dapagliflozin increased urinary glucose excretion by 217.2 mmol/24 h (95% confidence interval (CI): from 155.7 to 278.7, p < 0.01) and urinary osmolality by 60.4 mOsmol/kg (from 30.0 to 90.9, p < 0.01), compared to placebo. Fractional lithium excretion increased by 19.6% (from 6.7 to 34.2; p < 0.01), suggesting inhibition of sodium reabsorption in the proximal tubule. Renin and copeptin increased by 46.9% (from 21.6 to 77.4, p < 0.01) and 33.0% (from 23.9 to 42.7, p < 0.01), respectively. Free water clearance (FWC) decreased by −885.3 mL/24 h (from −1156.2 to −614.3, p < 0.01). These changes in markers of volume status suggest that dapagliflozin exerts both osmotic and natriuretic diuretic effects in patients with type 2 diabetes and kidney damage, as reflected by increased urinary osmolality and fractional lithium excretion. As a result, compensating mechanisms are activated to retain sodium and water.
机译:钠葡萄糖共转运蛋白2(SGLT2)抑制剂可降低2型糖尿病患者发生心肾衰竭的风险,这可能是由于利尿作用所致。先前使用SGLT2抑制剂进行的非安慰剂对照研究观察到健康个体和肾功能得以保留的2型糖尿病患者体内的体积标志物变化。目前尚不清楚2型糖尿病和肾脏损害的征兆是否表现出相似的变化。因此,对两项随机对照试验(n = 69)进行了事后分析,评估了达格列净10 mg /天与2型糖尿病患者的肾素-血管紧张素系统抑制作用合用时尿白蛋白与肌酐比值≥的效果。 30毫克/克。在治疗期开始和结束的六到十二周内采集血液和24小时尿液。确定了达格列净与安慰剂相比对各种容量状态指标的影响。在33例患者中评估了分数锂排泄,这是近端肾小管钠吸收的标志。达格列净使尿葡萄糖排泄增加217.2 mmol / 24 h(95%置信区间(CI):从155.7至278.7,p <0.01),尿渗透压升高60.4 mOsmol / kg(从30.0至90.9,p <0.01)安慰剂。锂的排泄分数增加了19.6%(从6.7增至34.2; p <0.01),表明抑制了近端小管中钠的重吸收。肾素和肽素分别增加了46.9%(从21.6增至77.4,p <0.01)和33.0%(从23.9增至42.7,p <0.01)。自由水清除率(FWC)降低了-885.3 mL / 24小时(从-1156.2降低到-614.3,p <0.01)。容量状态标志物的这些变化表明,达格列净对2型糖尿病和肾脏损害的患者具有渗透性和利钠利尿作用,如尿渗透压升高和锂排泄分数升高所反映。结果,激活了补偿机制以保留钠和水。

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