Key result
In patients with type 2 diabetes and high cardiovascular risk, liraglutide reduced the incidence of first and recurrent myocardial infarctions compared to placebo.
Why the study?
Does liraglutide reduce the incidence of first and recurrent myocardial infarctions in patients with type 2 diabetes mellitus and high cardiovascular risk?
RCT (n=9,340)
Does liraglutide reduce the incidence of first and recurrent myocardial infarctions in patients with type 2 diabetes mellitus and high cardiovascular risk?
In patients with type 2 diabetes and high cardiovascular risk, liraglutide reduces the overall incidence of first and recurrent myocardial infarctions compared to placebo.
Answers are grounded in this paper and cite their sources.
Supports liraglutide to lower MI risk in high-risk type 2 diabetes; confirms cardiovascular benefit in randomized evidence.
Diabetes mellitus (DM) is a known risk factor for myocardial infarction (MI); however, data regarding MI subtypes in people with diabetes are limited. In the Liraglutide Effect and Action in Diabetes: Evaluation of Cardiovascular Outcome Results (LEADER) trial (n = 9,340), liraglutide significantly reduced the risk of major adverse cardiovascular (CV) events (composite of CV death, nonfatal MI, or nonfatal stroke) versus placebo in patients with type 2 DM and high CV risk. Liraglutide also reduced risk of first MI (292 events with liraglutide vs 339 with placebo). This post hoc analysis characterized MIs (first and recurrent) occurring in LEADER, by treatment arm and regarding incidence, outcome, subtype, and troponin levels. A total of 780 MIs (first and recurrent) were reported, with fewer in the liraglutide-treatment group than in the placebo-treatment group (359 vs 421, p = 0.022). Numerically fewer MIs were associated with CV death with liraglutide than with placebo (17 vs 28 fatal MIs, p = 0.28). Symptomatic MIs in both arms were mainly non-ST-segment elevation MI (555/641) and spontaneous MI (518/641). Numerically greater proportions of symptomatic MIs were associated with troponin levels ≤5× or ≤10× the upper reference limit with liraglutide versus placebo (p = 0.16 and p = 0.42, respectively). At baseline, more liraglutide-treated patients than placebo-treated patients with MI during the trial had a history of coronary artery bypass graft (p = 0.008), and fewer had peripheral arterial disease in the lower extremities (p = 0.005) and >50% stenosis of the coronary artery, the carotid artery, or other arteries (p = 0.044). In conclusion, this analysis showed that liraglutide reduces the incidence of MIs in patients with type 2 DM at high CV risk and may impact the clinical outcomes of MI.
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Marso et al. (2018) conducted an RCT in Type 2 diabetes mellitus and high cardiovascular risk (n=9,340). Liraglutide vs. Placebo was evaluated on First and recurrent myocardial infarctions (p=0.022). In patients with type 2 diabetes and high cardiovascular risk, liraglutide reduced the incidence of first and recurrent myocardial infarctions compared to placebo.
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