Key result
GLP-1 receptor agonist use linked to ~28% lower post-MI cardiovascular risk in diabetes.
Why the study?
Trial evidence indicated GLP-1 RAs may reduce cardiovascular events in patients with diabetes and MI, but evaluation was needed in routine care settings.
Does the use of GLP-1 RAs reduce cardiovascular events in patients with diabetes surviving an acute myocardial infarction?
Cohort (n=17,868)
Yes
Does the use of GLP-1 RAs reduce cardiovascular events in patients with diabetes surviving an acute myocardial infarction?
Hazard Ratio: 0.72 (95% CI 0.56–0.92)
Absolute Event Rate: 97.91% vs 148.69%
Use of GLP-1 receptor agonists in routine care is associated with a lower risk of major adverse cardiovascular events in diabetic patients following a myocardial infarction.
GLP-1 RA use was associated with lower post-MI MACE in diabetes; extends observational data but leaves open causality and need for RCTs.
AIMS: Trial evidence indicates that glucagon-like peptide-1 receptor agonists (GLP-1 RAs) may reduce the risk of cardiovascular (CV) events in patients with diabetes and myocardial infarction (MI). We aimed to expand this observation to routine care settings. METHODS AND RESULTS: Prospective observational study including all patients with diabetes surviving an MI and registered in the nationwide SWEDEHEART registry during 2010-17. Multivariable Cox regression analyses were used to estimate the association between GLP-1 RAs use and the study outcome, which was a composite of stroke, heart failure, Re-infarction, or CV death. Covariates included demographics, comorbidities, presentation at admission, and use of secondary CV prevention therapies. In total, 17 868 patients with diabetes were discharged alive after a first event of MI. Their median age was 71 years, 36% were women and their median estimated glomerular filtration rate was 75 mL/min/1.73m2. Of those, 365 (2%) were using GLP-1 RAs. During median 3 years of follow-up, 7005 patients experienced the primary composite outcome. Compared with standard of diabetes care, use of GLP-1 RAs was associated with a lower event risk [adjusted hazard ratio (HR) 0.72; 95% confidence interval (CI): 0.56-0.92], mainly attributed to a lower rate of re-infarction and stroke. Results were similar after propensity score matching or when compared with users of sulfonylurea. There was no suggestion of heterogeneity across subgroups of age, sex, chronic kidney disease, and STEMI. CONCLUSION: GLP-1 RAs use, compared with standard of diabetes care, was associated with lower risk for major CV events in healthcare-managed survivors of an MI.
No takes yet. Share an insight, caveat, or question.
Trevisan et al. (2020) conducted a cohort in Diabetes surviving an acute myocardial infarction (n=17,868). Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) vs. Standard of diabetes care (non-use) was evaluated on Composite of non-fatal stroke, heart failure, myocardial re-infarction, or cardiovascular death (Adjusted HR 0.72, 95% CI 0.56-0.92). Use of GLP-1 receptor agonists in patients with diabetes surviving a myocardial infarction was associated with a 28% lower risk of the primary composite cardiovascular outcome (HR 0.72).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: