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利拉鲁肽对 2 型糖尿病患者心血管事件和死亡率的影响:系统评价和随机对照试验的荟萃分析。

Effects of exenatide long-acting release on cardiovascular events and mortality in patients with type 2 diabetes: a systematic review and meta-analysis of randomized controlled trials.

机构信息

Department of Medicine, University of Padova, Via Giustiniani 2, 35128, Padua, Italy.

出版信息

Acta Diabetol. 2019 Sep;56(9):1051-1060. doi: 10.1007/s00592-019-01347-0. Epub 2019 Apr 16.

DOI:10.1007/s00592-019-01347-0
PMID:30993527
Abstract

AIMS

Patients with type 2 diabetes (T2D) have an increased risk of cardiovascular disease. Recent cardiovascular outcome trials (CVOTs) with liraglutide, semaglutide, and albiglutide have shown significant reduction in major adverse cardiovascular events. Conversely, the CVOT with exenatide long-acting release (ELAR) confirmed cardiovascular safety of the drug, but did not reached superiority versus placebo. Herein, we systematically evaluated the effect of ELAR versus placebo or active comparators on cardiovascular events and mortality in patients with T2D.

METHODS

We screened the literature for randomized controlled trials reporting cardiovascular events and deaths in patients receiving ELAR versus those receiving placebo or any other glucose-lowering medications. Event rates were pooled and compared using the random-effects model.

RESULT

We retrieved 16 trials comparing the occurrence of cardiovascular events and mortality in patients treated with ELAR versus placebo or active comparators. The pooled rate ratio for cardiovascular events was similar in the two groups (0.99; 95% CI 0.92-1.06). The rate ratio for all-cause mortality was significantly lower in exenatide group than in comparators (0.87; 95% CI 0.77-0.97). When results of the EXSCEL trial were omitted, the pooled rate ratio for cardiovascular events and mortality was 0.80 (95% CI 0.40-1.63) and 0.75 (95% CI 0.30-1.84), respectively.

CONCLUSIONS

Treatment with ELAR does not increase the risk of cardiovascular events and may reduce all-cause mortality.

摘要

目的

2 型糖尿病(T2D)患者发生心血管疾病的风险增加。最近的利拉鲁肽、司美格鲁肽和阿必鲁肽心血管结局试验(CVOT)显示,主要不良心血管事件显著减少。相反,艾塞那肽长效释放制剂(ELAR)的 CVOT 证实了该药物的心血管安全性,但未优于安慰剂。在此,我们系统评估了 ELAR 与安慰剂或阳性对照药物在 T2D 患者中的心血管事件和死亡率的影响。

方法

我们对报告 ELAR 治疗患者与安慰剂或任何其他降糖药物治疗患者心血管事件和死亡的随机对照试验进行了文献筛选。使用随机效应模型对事件发生率进行了汇总和比较。

结果

我们检索到 16 项比较 ELAR 治疗患者与安慰剂或阳性对照药物发生心血管事件和死亡率的试验。两组心血管事件的合并率比相似(0.99;95%CI 0.92-1.06)。与对照药物相比,艾塞那肽组的全因死亡率显著降低(0.87;95%CI 0.77-0.97)。当排除 EXSCEL 试验的结果时,心血管事件和死亡率的合并率比分别为 0.80(95%CI 0.40-1.63)和 0.75(95%CI 0.30-1.84)。

结论

ELAR 治疗不会增加心血管事件的风险,并且可能降低全因死亡率。

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