Key result
GLP-1 agonists significantly improved left ventricular ejection fraction (MD 2.81) and reduced final infarct size (MD -5.71 g) compared to control in patients with acute myocardial infarction undergoing PCI or CABG.
Why the study?
Controversy exists on the cardioprotective effects of GLP-1 against ischemia-reperfusion injury in AMI patients undergoing PCI and CABG surgery.
Does GLP-1 infusion or its receptor agonists improve LVEF and reduce infarct size in adult patients with AMI undergoing PCI or CABG?
Meta-Analysis (n=1,216)
Does GLP-1 infusion or its receptor agonists improve LVEF and reduce infarct size in adult patients with AMI undergoing PCI or CABG?
In patients with AMI undergoing PCI or CABG, GLP-1 administration is associated with improved LVEF, reduced infarct size, and lower MACE risk, despite increased gastrointestinal side effects.
Answers are grounded in this paper and cite their sources.
Supports adjunctive GLP-1 agonists in AMI revascularization; extends meta-analytic evidence for LVEF recovery and infarct reduction.
Glucagon-like peptide-1 (GLP-1) protects against ischemia-reperfusion injury in patients with acute myocardial infarction (AMI). Controversy exists on the effects of GLP-1 on AMI patients undergoing percutaneous coronary intervention (PCI) and coronary artery bypass graft (CABG) surgery. We aimed to investigate the cardioprotective effects of GLP-1 in AMI patients after PCI and CABG. We searched PubMed, Web of Science, EBSCO, Scopus, and the Cochrane Library for relevant randomized controlled trials (RCTs) up to June 2021, with no restriction on publication date. The following search terms are used: “percutaneous coronary intervention” or “coronary artery bypass grafting” or “myocardial infarction” and “glucagon-like peptide 1” or “exenatide” or “liraglutide”. Articles were independently assessed by 2 reviewers. We included RCTs only that compared GLP-1 with control in AMI patients. Continuous data were pooled as mean differences (MDs), while dichotomous variables were pooled as odds ratios (ORs), with 95% confidence interval (CI), using R software (meta package) for windows. Subgroup analysis according to the intervention type and GLP-agents were conducted. We assessed the heterogeneity among RCTs using the Q statistic and I2 statistic. We also tested publication bias by funnel plot–based methods. The quality of each study was assessed with the Cochrane risk of bias tool. Primary outcomes were changes of left ventricular ejection fraction (LVEF), myocardial infarct characteristics, salvage index. Secondary outcomes included major adverse cardiac events (MACE), gastrointestinal events, and hypoglycemia. Nine RCTs (14 reports) including 1216 patients were included in this meta-analysis. At 3 months follow up, GLP-1 was associated with improved LVEF (MD = 2.81, 95% CI [0.69, 4.94]), infarct size in grams (MD = −5.71, 95% CI [−10.24, −1.18]), and salvage index (MD = 0.09, 95% CI [0.05, 0.14]). While, GLP-1 had less MACE rate than control (RR = 0.64, 95% CI [0.41, 0.99]), and higher gastrointestinal side effects (RR = 4.21, 95% CI [2.39, 7.41]). This meta-analysis illustrated that GLP-1 was associated with better LVEF and reduced infarct size in patients with AMI undergoing PCI and CABG surgery, although the mechanism on how this agent provide this benefit is not clear. Question: What is the effectiveness of Glucagon-like peptide-1 (GLP-1) agonist in patients with acute myocardial infarction (AMI) undergoing percutaneous coronary intervention (PCI) and coronary artery bypass graft (CABG) surgery. Findings: This systematic review and meta-analysis illustrated that GLP-1 was associated with better left ventricular ejection fraction and reduced infarct size in patients with AMI undergoing PCI and CABG surgery, probably by reducing reperfusion injury. Meaning: GLP-1 could improve systolic and diastolic function, lowering the cardiovascular risk of morbidity and mortality in AMI patients.
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Ogbu et al. (2021) conducted a meta-analysis in Acute myocardial infarction (AMI) undergoing percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG) (n=1,216). Glucagon-like peptide-1 (GLP-1) agonist vs. Placebo or insulin was evaluated on Change in left ventricular ejection fraction (LVEF) at 3 months (MD 2.81, 95% CI 0.69, 4.94). GLP-1 agonists significantly improved left ventricular ejection fraction (MD 2.81) and reduced final infarct size (MD -5.71 g) compared to control in patients with acute myocardial infarction undergoing PCI or CABG.
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