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Antihyperglycemic Medications and Cardiovascular Risk Reduction.

Eur Endocrinol · 2017

Last updated 2026-05-28

Since 2008, the FDA has required new diabetes drugs to prove they don’t increase heart disease risk. Four GLP-1 drugs—liraglutide and semaglutide—and two SGLT2 drugs—canagliflozin and empagliflozin—have shown they can reduce major heart events like heart attack, stroke, or heart-related death by about 12% to 26% compared to a placebo in people with type 2 diabetes who already have heart disease or are at high risk.

AI summary of the abstract below.

JournalEur Endocrinol, 2017
Citations9
Relative citation ratio0.29
NIH percentile18
Molecules
Conditions studied Type 2 Diabetes, Cardiovascular Risk Reduction

Abstract

Cardiovascular disease (CVD) remains a leading cause of death in patients with type 2 diabetes (T2D). In addition to glycemic control, a major focus of diabetes treatment involves cardiovascular (CV) risk reduction. In 2008, the US Food and Drug Administration (FDA) instituted a new requirement that new drugs developed and studied for the treatment of T2D must undergo CV safety testing. Since the advent of this new policy, canagliflozin, empagliflozin, liraglutide and semaglutide have demonstrated superior CV event reduction - via a composite of reduction in CV death, nonfatal myocardial infarction (MI), and nonfatal stroke - compared with placebo in patients with T2D and existing CVD, or at high risk of CVD. Multiple studies are underway to evaluate the CV outcomes of other antihyperglycemic agents. In a time when there are numerous drugs in the T2D armamentarium, positive CV outcomes data influence drug selection and aids practitioners in making more individualised therapeutic recommendations for their patients.

Verbatim abstract via PubMed 29632614 ↗