Heise Tim, Jordan Jens, Wanner Christoph, Heer Martina, Macha Sreeraj, Mattheus Michaela, Lund Søren S, Woerle Hans J, Broedl Uli C
Profil, Neuss, Germany.
Institute of Clinical Pharmacology, Hannover Medical School, Hannover, Germany.
Clin Ther. 2016 Oct;38(10):2265-2276. doi: 10.1016/j.clinthera.2016.09.001. Epub 2016 Sep 28.
Our aim was to investigate the effects of the sodium glucose cotransporter 2 inhibitor empagliflozin on urinary and serum glucose and electrolytes, urinary volume, osmolality, and the renin-angiotensin system in patients with type 2 diabetes.
In an open-label study, 22 patients receiving metformin (median age 56 years; range 40-65 years) received empagliflozin 25 mg once daily for 5 days. Food, fluid, and sodium intake were standardized for 3 days before and during treatment.
Twenty patients completed treatment. After single and multiple doses of empagliflozin, mean (SE) changes from baseline in 24-hour urinary glucose excretion were 463.3 (57.3) mmol/d and 599.5 (60.0) mmol/d, respectively (83.5 [10.3] g/d and 108.0 [10.8] g/d, respectively) (both P < 0.001), and in fasting serum glucose concentration were -1.8 (0.4) mmol/L and -1.1 (0.3) mmol/L, respectively (both P < 0.001). After a single dose, mean (SE) change from baseline in urine sodium excretion was 45.3 (9.6) mmol/d (P < 0.001), and in urine volume was 341.0 (140.5) g/d (P = 0.025), but there were no changes compared with baseline in either parameter after multiple doses. There were no changes in plasma renin or serum aldosterone with single or multiple doses of empagliflozin. There was a nonsignificant reduction in weight after a single dose of empagliflozin and a mean (SE) change of -1.4 (0.5) kg after multiple doses (P = 0.020).
Empagliflozin 25 mg increased urinary glucose excretion and decreased serum glucose and weight with transient natriuresis and increases in urine volume, without significant changes in the renin-angiotensin system. Clinicaltrials.gov Identifier: NCT01276288.
我们的目的是研究钠-葡萄糖协同转运蛋白2抑制剂恩格列净对2型糖尿病患者尿糖、血糖、电解质、尿量、渗透压以及肾素-血管紧张素系统的影响。
在一项开放标签研究中,22例接受二甲双胍治疗的患者(中位年龄56岁;范围40 - 65岁)每天服用一次25 mg恩格列净,共5天。在治疗前和治疗期间,食物、液体和钠的摄入量均标准化3天。
20例患者完成治疗。单次和多次服用恩格列净后,24小时尿葡萄糖排泄量较基线的平均(标准误)变化分别为463.3(57.3)mmol/d和599.5(60.0)mmol/d(分别为83.5 [10.3] g/d和108.0 [10.8] g/d)(均P < 0.001),空腹血糖浓度较基线的平均(标准误)变化分别为 -1.8(0.4)mmol/L和 -1.1(0.3)mmol/L(均P < 0.001)。单次给药后,尿钠排泄量较基线的平均(标准误)变化为45.3(9.6)mmol/d(P < 0.001),尿量较基线的平均(标准误)变化为341.0(140.5)g/d(P = 0.025),但多次给药后这两个参数与基线相比均无变化。单次或多次服用恩格列净后,血浆肾素或血清醛固酮均无变化。单次服用恩格列净后体重有非显著性下降,多次服用后平均(标准误)变化为 -1.4(0.5)kg(P = 0.020)。
25 mg恩格列净可增加尿葡萄糖排泄,降低血糖和体重,伴有短暂性利钠作用和尿量增加,而肾素-血管紧张素系统无显著变化。Clinicaltrials.gov标识符:NCT01276288。