Protective effect of glucagon-like peptide-1 agents on reperfusion injury for acute myocardial infarction: a meta-analysis of randomized controlled trials

Ann Med. 2017 Nov;49(7):552-561. doi: 10.1080/07853890.2017.1306653. Epub 2017 Mar 31.

Abstract

Background: The cardioprotective properties of glucagon-like peptide-1 (GLP-1) receptor agonists in acute myocardial infarction (AMI) patients against reperfusion injury remain unclear. We performed a meta-analysis to assess their role in the acute phase of AMI.

Methods and results: Randomized controlled trials (RCTs) comparing GLP-1 agents with placebo in AMI patients undergoing percutaneous coronary intervention were identified by searching PubMed, Embase and Cochrane libraries. Six RCTs with 800 patients were included in the meta-analysis. Compared with placebo, GLP-1 agents improved left ventricular ejection fraction (LVEF) by 2.46 [95% confidence interval (CI): 0.23-4.70%] and reduced the infarct size in grams as well as in percentage of the area at risk [weighted mean difference (WMD) - 5.29, 95% CI: -10.39 to -0.19; WMD -0.08, 95% CI: -0.12 to -0.04, respectively]. The incidence of cardiovascular events appeared to be lower with GLP-1 therapy, but the statistical significance was not reached [relative risk (RR): 0.78; 95% CI: 0.58-1.06]. In terms of safety evaluation, GLP-1 treatment increased the risk of gastrointestinal adverse events (RR: 5.50, 95% CI: 2.85-10.60).

Conclusions: Our analysis shows that in patients with AMI undergoing PCI, GLP-1 treatment is associated with improved LVEF and reduced infarct size.

Trial registration: ClinicalTrials.gov NCT02001363 NCT00835848 NCT01254123 NCT01580514.

Keywords: Glucagon-like peptide-1; acute myocardial infarction; meta-analysis.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Gastrointestinal Tract / drug effects
  • Glucagon-Like Peptide 1 / analogs & derivatives*
  • Glucagon-Like Peptide-1 Receptor / agonists*
  • Humans
  • Incidence
  • Myocardial Infarction / complications
  • Myocardial Infarction / epidemiology
  • Myocardial Infarction / therapy*
  • Percutaneous Coronary Intervention
  • Protective Agents / pharmacology
  • Protective Agents / therapeutic use*
  • Randomized Controlled Trials as Topic
  • Reperfusion Injury / etiology
  • Reperfusion Injury / prevention & control*
  • Stroke Volume / drug effects
  • Ventricular Function, Left / drug effects

Substances

  • GLP1R protein, human
  • Glucagon-Like Peptide-1 Receptor
  • Protective Agents
  • Glucagon-Like Peptide 1

Associated data

  • ClinicalTrials.gov/NCT02001363
  • ClinicalTrials.gov/NCT00835848
  • ClinicalTrials.gov/NCT01254123
  • ClinicalTrials.gov/NCT01580514