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西格列汀与开放标签 SGLT2 抑制剂平行或序贯治疗对 2 型糖尿病患者死亡率及心肾结局的影响:来自 EXSCEL 试验的结果。

Effects of exenatide and open-label SGLT2 inhibitor treatment, given in parallel or sequentially, on mortality and cardiovascular and renal outcomes in type 2 diabetes: insights from the EXSCEL trial.

机构信息

Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca, 1 MedImmune Way, Gaithersburg, MD, 20878, USA.

Clinical Pharmacology and Safety Sciences, R&D, AstraZeneca, Boston, USA.

出版信息

Cardiovasc Diabetol. 2019 Oct 22;18(1):138. doi: 10.1186/s12933-019-0942-x.

Abstract

BACKGROUND

Sodium-glucose cotransporter-2 inhibitors (SGLT2i) and glucagon-like peptide-1 receptor agonists (GLP-1 RA) improve cardiovascular and renal outcomes in patients with type 2 diabetes through distinct mechanisms. However, evidence on clinical outcomes in patients treated with both GLP-1 RA and SGLT2i is lacking. We aim to provide insight into the effects of open-label SGLT2i use in parallel with or shortly after once-weekly GLP-1 RA exenatide (EQW) on cardiorenal outcomes.

METHODS

In the EXSCEL cardiovascular outcomes trial EQW arm, SGLT2i drop-in occurred in 8.7% of participants. These EQW+SGLT2i users were propensity-matched to: (1) placebo-arm participants not taking SGLT2i (n = 572 per group); and to (2) EQW-arm participants not taking SGLT2i (n = 575), based on their last measured characteristics before SGLT2i initiation, and equivalent study visit in comparator groups. Time-to-first major adverse cardiovascular event (MACE) and all-cause mortality (ACM) were compared using Cox regression analyses. eGFR slopes were quantified using mixed model repeated measurement analyses.

RESULTS

In adjusted analyses, the risk for MACE with combination EQW+SGLT2i use was numerically lower compared with both placebo (adjusted hazard ratio 0.68, 95% CI 0.39-1.17) and EQW alone (0.85, 0.48-1.49). Risk of ACM was nominally significantly reduced compared with placebo (0.38, 0.16-0.90) and compared with EQW (0.41, 0.17-0.95). Combination EQW+SGLT2i use also nominally significantly improved estimated eGFR slope compared with placebo (+ 1.94, 95% CI 0.94-2.94 mL/min/1.73 m/year) and EQW alone (+ 2.38, 1.40-3.35 mL/min/1.73 m/year).

CONCLUSIONS

This post hoc analysis supports the hypothesis that combinatorial EQW and SGLT2i therapy may provide benefit on cardiovascular outcomes and mortality. Trial registration Clinicaltrials.gov, Identifying number: NCT01144338, Date of registration: June 15, 2010.

摘要

背景

钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)和胰高血糖素样肽-1 受体激动剂(GLP-1 RA)通过不同的机制改善 2 型糖尿病患者的心血管和肾脏结局。然而,关于同时接受 GLP-1 RA 和 SGLT2i 治疗的患者的临床结局证据尚缺乏。我们旨在深入了解在每周一次 GLP-1 RA 艾塞那肽(EQW)治疗期间或之后不久开始使用 SGLT2i 的开放标签使用对心肾结局的影响。

方法

在 EXSCEL 心血管结局试验的 EQW 臂中,8.7%的参与者开始使用 SGLT2i。这些 EQW+SGLT2i 用户与:(1)未服用 SGLT2i 的安慰剂组参与者(每组 572 人);和(2)未服用 SGLT2i 的 EQW 组参与者(每组 575 人)进行了倾向评分匹配,这是基于他们在开始使用 SGLT2i 之前的最后一次测量特征,以及在比较组中进行了等效的研究访问。使用 Cox 回归分析比较首次主要不良心血管事件(MACE)和全因死亡率(ACM)的时间。使用混合模型重复测量分析量化 eGFR 斜率。

结果

在调整后的分析中,与安慰剂相比(调整后的危险比 0.68,95%CI 0.39-1.17)和与 EQW 单独使用相比(0.85,0.48-1.49),联合使用 EQW+SGLT2i 的 MACE 风险数值较低。与安慰剂(0.38,0.16-0.90)和 EQW(0.41,0.17-0.95)相比,ACM 风险名义上显著降低。与安慰剂(+1.94,95%CI 0.94-2.94 mL/min/1.73 m/year)和 EQW 单独使用(+2.38,1.40-3.35 mL/min/1.73 m/year)相比,联合使用 EQW+SGLT2i 也可名义上显著改善估计的 eGFR 斜率。

结论

这项事后分析支持以下假设,即联合使用 EQW 和 SGLT2i 治疗可能对心血管结局和死亡率有益。

试验注册

Clinicaltrials.gov,识别号:NCT01144338,注册日期:2010 年 6 月 15 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfb5/6805385/54fcfd950f84/12933_2019_942_Fig1_HTML.jpg

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