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Glucagon-like peptide-1 receptor agonists and heart failure in type 2 diabetes: Systematic review and meta-analysis of randomized and observational studies

  • Ling Li
  • , Sheyu Li
  • , Jiali Liu
  • , Ke Deng
  • , Jason W. Busse
  • , Per Olav Vandvik
  • , Evelyn Wong
  • , Zahra N. Sohani
  • , Malgorzata M. Bala
  • , Lorena P. Rios
  • , German Malaga
  • , Shanil Ebrahim
  • , Jiantong Shen
  • , Longhao Zhang
  • , Pujing Zhao
  • , Qunfei Chen
  • , Yingqiang Wang
  • , Gordon H. Guyatt
  • , Xin Sun
  • Sichuan University
  • West China School of Pharmacy
  • McMaster University
  • McMaster University
  • Norwegian Knowledge Centre for the Health Services
  • Innlandet Hospital Trust
  • University of British Columbia
  • University of Toronto Faculty of Medicine
  • Jagiellonian University Medical College
  • Hospital Clinico FUSAT
  • Stanford University School of Medicine
  • Hospital for Sick Kids
  • Lanzhou University
  • Department of Medical Administration

Research output: Contribution to journalArticlepeer-review

40 Scopus citations

Abstract

Background: The effect of glucagon-like peptide-1(GLP-1) receptor agonists on heart failure remains uncertain. We therefore conducted a systematic review to assess the possible impact of GLP-1 agonists on heart failure or hospitalization for heart failure in patients with type 2 diabetes. Methods: We searched MEDLINE, EMBASE, the Cochrane Central Register of Controlled Trials (CENTRAL) and ClinicalTrials.gov to identify randomized controlled trials (RCTs) and observational studies that addressed the effect of GLP-1 receptor agonists in adults with type 2 diabetes, and explicitly reported heart failure or hospitalization for heart failure. Two paired reviewers screened reports, collected data, and assessed the risk of bias. We pooled data from RCTs and observational studies separately, and used the GRADE approach to rate the quality of evidence. Results: We identified 25 studies that were eligible for our review; 21 RCTs (n = 18,270) and 4 observational studies (n = 111,029). Low quality evidence from 20 RCTs suggested, if anything, a lower incidence of heart failure between GLP-1 agonists versus control (17/7,441 vs. 19/4,317; odds ratio (OR) 0.62, 95 % confidence interval (CI) 0.31 to 1.22; risk difference (RD) 19 fewer, 95 % CI 34 fewer to 11 more per 1000 over 5 years). Three cohort studies comparing GLP-1 agonists to alternative agents provided very low quality evidence that GLP-1 agonists do not increase the incidence of heart failure. One RCT provided moderate quality evidence that GLP-1 agonists were not associated with hospitalization for heart failure (lixisenatide vs placebo: 122/3,034 vs. 127/3,034; adjusted hazard ratio 0.96, 95 % CI 0.75 to 1.23; RD 4 fewer, 95 % CI 25 fewer to 23 more per 1000 over 5 years) and a case-control study provided very low quality evidence also suggesting no association (GLP-1 agonists vs. other anti-hyperglycemic drugs: 1118 cases and 17,626 controls, adjusted OR 0.67, 95 % CI 0.32 to 1.42). Conclusions: The current evidence suggests that GLP-1 agonists do not increase the risk of heart failure or hospitalization for heart failure among patients with type 2 diabetes.

Original languageEnglish
Article number91
JournalBMC Cardiovascular Disorders
Volume16
Issue number1
DOIs
StatePublished - 2016

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Glucagon-like peptide-1 receptor
  • Heart failure
  • Meta-analysis
  • Systematic review
  • Type 2 diabetes

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