Glucagon-Like Peptide-1 Receptor Agonists Across the Spectrum of Heart Failure

Author:

Ferreira João Pedro123ORCID,Sharma Abhinav4ORCID,Butler Javed5ORCID,Packer Milton67ORCID,Zannad Faiez2ORCID,Vasques-Nóvoa Francisco18,Leite-Moreira Adelino1,Neves João Sérgio19

Affiliation:

1. UnIC@RISE, Department of Surgery and Physiology, Cardiovascular Research and Development Center, University of Porto , Porto , Portugal

2. Université de Lorraine, Inserm, Centre d’Investigations Cliniques Plurithématique 1433, and Inserm U1116, CHRU, F-CRIN INI-CRCT (Cardiovascular and Renal Clinical Trialists) , Nancy , France

3. Heart Failure Clinic, Centro Hospitalar de Vila Nova de Gaia/Espinho , Vila Nova de Gaia , Portugal

4. Centre for Outcomes Research and Evaluation Research Institute of the McGill University Health Centre, Division of Cardiology McGill University Health Centre McGill University, DREAM-CV Laboratory McGill University Health Centre McGill University , Montreal, QC , Canada

5. Baylor Scott and White Research Institute , Dallas, TX , USA

6. Baylor Heart and Vascular Institute, Baylor University Medical Center , Dallas, TX , USA

7. Imperial College , London , UK

8. Department of Internal Medicine, Centro Hospitalar Universitário de São João , Porto , Portugal

9. Department of Endocrinology, Diabetes and Metabolism, Centro Hospitalar Universitário de São João , Porto , Portugal

Abstract

Abstract Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) have been used to reduce body weight in overweight or people with obesity and to improve glycemic control and cardiovascular outcomes among people with type 2 diabetes (T2D) and a high cardiovascular risk. However, the effects of GLP-1 RAs may be modified by the presence of heart failure (HF). In this review, we summarize the evidence for the use of GLP-1 RA across a patient's risk with a particular focus on HF. After a careful review of the literature, we challenge the current views about the use of GLP-1 RAs and suggest performing active HF screening (with directed clinical history, physical examination, an echocardiogram, and natriuretic peptides) before initiating a GLP-1 RA. After HF screening, we suggest GLP-1 RA treatment decisions as follows: (1) in people with T2D without HF, GLP-1 RAs should be used for reducing the risk of myocardial infarction and stroke, with a possible effect to reduce the risk of HF hospitalizations; (2) in patients with HF and preserved ejection fraction, GLP-1 RAs do not reduce HF hospitalizations but may reduce atherosclerotic events, and their use may be considered in an individualized manner; and (3) in patients with HF and reduced ejection fraction, the use of GLP-1 RAs warrants caution due to potential risk of worsening HF events and arrhythmias, pending risk–benefit data from further studies.

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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