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Cardioprotective anti-hyperglycaemic medications: a review of clinical trials.

Eur Heart J · 2018

Last updated 2026-07-14

Four major clinical trials (EMPA-REG, CANVAS, LEADER, and SUSTAIN-6) found that certain diabetes medications—empagliflozin, canagliflozin, liraglutide, and semaglutide—reduced cardiovascular events in people with type 2 diabetes. Based on these results, the FDA approved empagliflozin to lower cardiovascular death risk in this group, marking the first diabetes drug approved for this purpose.

AI summary of the abstract below.

JournalEur Heart J, 2018
Citations33
Relative citation ratio1.21
NIH percentile57
Molecules

Abstract

Despite extensive clinical efforts to achieve stricter glycaemic control over the past few decades, cardiovascular (CV) disease remains the leading cause of death among diabetic patients. Recently, sodium-glucose cotransporter-2 (SGLT-2) inhibitors and glucagon-like peptide-1 receptor (GLP-1-R) agonists have gained attention due to their apparent effects in reducing CV mortality. Four CV randomized controlled trials: EMPA-REG, CANVAS, LEADER, and SUSTAIN-6, found a decrease in CV events among patients with type 2 diabetes on empagliflozin, canagliflozin, liraglutide, and semaglutide, respectively. In light of this data, the US Food and Drug Administration has recently approved empagliflozin for CV mortality reduction in type 2 diabetic patients, making it the first diabetes medication approved for such an indication. The purpose of this review is to summarize the results of novel anti-hyperglycaemic medication trials, and shed light on their mode of action and cardioprotective pathways.

Verbatim abstract via PubMed 29236983 ↗