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达格列净、艾塞那肽及其联合应用对 2 型糖尿病患者尿白蛋白排泄的影响:一项随机交叉临床试验研究。

Albuminuria-lowering effect of dapagliflozin, exenatide, and their combination in patients with type 2 diabetes: A randomized cross-over clinical study.

机构信息

Department of Clinical Pharmacy and Pharmacology, University of Groningen, Groningen, The Netherlands.

Department of Clinical Pharmacy, Martini Hospital, Groningen, The Netherlands.

出版信息

Diabetes Obes Metab. 2023 Jun;25(6):1758-1768. doi: 10.1111/dom.15033. Epub 2023 Mar 13.

Abstract

AIM

To evaluate the albuminuria-lowering effect of dapagliflozin, exenatide, and the combination of dapagliflozin and exenatide in patients with type 2 diabetes and microalbuminuria or macroalbuminuria.

METHODS

Participants with type 2 diabetes, an estimated glomerular filtration rate (eGFR) of more than 30 ml/min/1.73m and an urinary albumin: creatinine ratio (UACR) of more than 3.5 mg/mmol and 100 mg/mmol or less completed three 6-week treatment periods, during which dapagliflozin 10 mg/d, exenatide 2 mg/wk and both drugs combined were given in random order. The primary outcome was the percentage change in UACR. Secondary outcomes included blood pressure, HbA1c, body weight, extracellular volume, fractional lithium excretion and renal haemodynamic variables as determined by magnetic resonance imaging.

RESULTS

We enrolled 20 patients, who completed 53 treatment periods in total. Mean percentage change in UACR from baseline was -21.9% (95% CI: -34.8% to -6.4%) during dapagliflozin versus -7.7% (95% CI: -23.5% to 11.2%) during exenatide and -26.0% (95% CI: -38.4% to -11.0%) during dapagliflozin-exenatide treatment. No correlation was observed in albuminuria responses between the different treatments. Numerically greater reductions in systolic blood pressure, body weight and eGFR were observed during dapagliflozin-exenatide treatment compared with dapagliflozin or exenatide alone. Renal blood flow and effective renal plasma flow (ERPF) did not significantly change with either treatment regimen. However, all but four and two patients in the dapagliflozin and dapagliflozin-exenatide groups, respectively, showed reductions in ERPF. The filtration fraction did not change during treatment with dapagliflozin or exenatide, and decreased during dapagliflozin-exenatide treatment (-1.6% [95% CI: -3.2% to -0.01%]; P = .048).

CONCLUSIONS

In participants with type 2 diabetes and albuminuria, treatment with dapagliflozin, exenatide and dapagliflozin-exenatide reduced albuminuria, with a numerically larger reduction in the combined dapagliflozin-exenatide treatment group.

摘要

目的

评估达格列净、艾塞那肽以及达格列净与艾塞那肽联合应用在合并微量白蛋白尿或大量白蛋白尿的 2 型糖尿病患者中的降蛋白尿作用。

方法

纳入估计肾小球滤过率(eGFR)超过 30ml/min/1.73m2 且尿白蛋白与肌酐比值(UACR)超过 3.5mg/mmol 但低于 100mg/mmol 的 2 型糖尿病患者,完成 3 个 6 周的治疗周期,分别随机接受达格列净 10mg/d、艾塞那肽 2mg/周和两种药物联合治疗。主要转归为 UACR 的百分比变化。次要转归包括血压、糖化血红蛋白(HbA1c)、体重、细胞外容量、锂排泄分数以及磁共振成像测定的肾血流动力学变量。

结果

共纳入 20 例患者,共完成 53 个治疗周期。与艾塞那肽组(-7.7%,95%CI:-23.5%至 11.2%)相比,达格列净组(-21.9%,95%CI:-34.8%至-6.4%)和达格列净与艾塞那肽联合组(-26.0%,95%CI:-38.4%至-11.0%)的 UACR 自基线的百分比变化更大。不同治疗方法之间的蛋白尿反应没有相关性。与单独使用达格列净或艾塞那肽相比,达格列净与艾塞那肽联合治疗时收缩压、体重和 eGFR 的降低更为显著。两种治疗方案均未显著改变肾血流量和有效肾血浆流量(ERPF)。然而,达格列净组和达格列净与艾塞那肽联合组分别有除 4 例和 2 例患者外,其余患者的 ERPF 均降低。治疗期间,达格列净或艾塞那肽治疗组的滤过分数无变化,而达格列净与艾塞那肽联合治疗组的滤过分数下降(-1.6%,95%CI:-3.2%至-0.01%;P=0.048)。

结论

在合并白蛋白尿的 2 型糖尿病患者中,达格列净、艾塞那肽和达格列净与艾塞那肽联合治疗均可降低白蛋白尿,联合治疗组的降幅更大。

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