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

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 R...

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Veröffentlicht in:The journal of clinical endocrinology and metabolism 2024-01, Vol.109 (1), p.4-9
Hauptverfasser: Ferreira, João Pedro, Sharma, Abhinav, Butler, Javed, Packer, Milton, Zannad, Faiez, Vasques-Nóvoa, Francisco, Leite-Moreira, Adelino, Neves, João Sérgio
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Sprache:eng
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Zusammenfassung: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.
ISSN:0021-972X
1945-7197
DOI:10.1210/clinem/dgad398