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SGLT-2 抑制剂与其他降血糖药物相关的心血管事件:CVD-REAL 2 研究。

Cardiovascular Events Associated With SGLT-2 Inhibitors Versus Other Glucose-Lowering Drugs: The CVD-REAL 2 Study.

机构信息

Department of Cardiovascular Disease, Saint Luke's Mid America Heart Institute and University of Missouri-Kansas City, Kansas City, Missouri.

National Heart Centre, Singapore and SingHealth Duke-NUS, Singapore; University Medical Centre Groningen, Groningen, the Netherlands.

出版信息

J Am Coll Cardiol. 2018 Jun 12;71(23):2628-2639. doi: 10.1016/j.jacc.2018.03.009. Epub 2018 Mar 11.

Abstract

BACKGROUND

Randomized trials demonstrated a lower risk of cardiovascular (CV) events with sodium-glucose cotransporter-2 inhibitors (SGLT-2i) in patients with type 2 diabetes (T2D) at high CV risk. Prior real-world data suggested similar SGLT-2i effects in T2D patients with a broader risk profile, but these studies focused on heart failure and death and were limited to the United States and Europe.

OBJECTIVES

The purpose of this study was to examine a broad range of CV outcomes in patients initiated on SGLT-2i versus other glucose-lowering drugs (oGLDs) across 6 countries in the Asia Pacific, the Middle East, and North American regions.

METHODS

New users of SGLT-2i and oGLDs were identified via claims, medical records, and national registries in South Korea, Japan, Singapore, Israel, Australia, and Canada. Propensity scores for SGLT-2i initiation were developed in each country, with 1:1 matching. Hazard ratios (HRs) for death, hospitalization for heart failure (HHF), death or HHF, MI, and stroke were assessed by country and pooled using weighted meta-analysis.

RESULTS

After propensity-matching, there were 235,064 episodes of treatment initiation in each group; ∼27% had established CV disease. Patient characteristics were well-balanced between groups. Dapagliflozin, empagliflozin, ipragliflozin, canagliflozin, tofogliflozin, and luseogliflozin accounted for 75%, 9%, 8%, 4%, 3%, and 1% of exposure time in the SGLT-2i group, respectively. Use of SGLT-2i versus oGLDs was associated with a lower risk of death (HR: 0.51; 95% confidence interval [CI]: 0.37 to 0.70; p < 0.001), HHF (HR: 0.64; 95% CI: 0.50 to 0.82; p = 0.001), death or HHF (HR: 0.60; 95% CI: 0.47 to 0.76; p < 0.001), MI (HR: 0.81; 95% CI: 0.74 to 0.88; p < 0.001), and stroke (HR: 0.68; 95% CI: 0.55 to 0.84; p < 0.001). Results were directionally consistent across both countries and patient subgroups, including those with and without CV disease.

CONCLUSIONS

In this large, international study of patients with T2D from the Asia Pacific, the Middle East, and North America, initiation of SGLT-2i was associated with a lower risk of CV events across a broad range of outcomes and patient characteristics. (Comparative Effectiveness of Cardiovascular Outcomes in New Users of SGLT-2 Inhibitors [CVD-REAL]; NCT02993614).

摘要

背景

随机试验表明,在心血管风险较高的 2 型糖尿病(T2D)患者中,钠-葡萄糖共转运蛋白-2 抑制剂(SGLT-2i)可降低心血管(CV)事件风险。先前的真实世界数据表明,SGLT-2i 在具有更广泛风险特征的 T2D 患者中具有类似的效果,但这些研究侧重于心力衰竭和死亡,并且仅限于美国和欧洲。

目的

本研究旨在研究亚太地区、中东和北美 6 个国家/地区新开始使用 SGLT-2i 与其他降血糖药物(oGLD)的患者的广泛 CV 结局。

方法

通过索赔、医疗记录和国家登记册,在韩国、日本、新加坡、以色列、澳大利亚和加拿大确定了 SGLT-2i 和 oGLD 的新使用者。在每个国家/地区制定了 SGLT-2i 起始的倾向评分,并进行了 1:1 匹配。使用加权荟萃分析按国家评估并汇总了死亡率、心力衰竭住院(HHF)、死亡或 HHF、心肌梗死(MI)和中风的风险比(HR)。

结果

在倾向匹配后,每组各有 235064 例治疗起始的发作;约 27%的患者有已确诊的 CV 疾病。两组患者的特征平衡良好。达格列净、恩格列净、依帕列净、卡格列净、托格列净和卢格列净分别占 SGLT-2i 组暴露时间的 75%、9%、8%、4%、3%和 1%。与 oGLD 相比,使用 SGLT-2i 与较低的死亡风险相关(HR:0.51;95%置信区间[CI]:0.37 至 0.70;p<0.001)、HFH(HR:0.64;95%CI:0.50 至 0.82;p=0.001)、死亡或 HFH(HR:0.60;95%CI:0.47 至 0.76;p<0.001)、MI(HR:0.81;95%CI:0.74 至 0.88;p<0.001)和中风(HR:0.68;95%CI:0.55 至 0.84;p<0.001)。结果在国家和患者亚组中均具有方向性一致性,包括有和没有 CV 疾病的患者。

结论

在这项来自亚太地区、中东和北美的 T2D 患者的大型国际研究中,SGLT-2i 的起始与广泛的 CV 结局和患者特征相关的 CV 事件风险降低相关。(新型 SGLT-2 抑制剂在心血管结局方面的比较效果[CVD-REAL];NCT02993614)。

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