Liraglutide in the treatment of heart failure: insight from FIGHT and LIVE.
Cardiovasc Diabetol · 2020
Last updated 2026-05-28A review of two studies (FIGHT and LIVE) found that liraglutide, a GLP-1 drug, did not improve heart function or blood sugar control in patients with heart failure. In the LIVE study, liraglutide increased heart rate and serious heart-related side effects, while improving walking distance and blood sugar levels.
AI summary of the abstract below.
| Journal | Cardiovasc Diabetol, 2020 |
|---|---|
| Citations | 14 |
| Relative citation ratio | 0.64 |
| NIH percentile | 36 |
| Molecules | liraglutide |
| Conditions studied | Heart Failure |
Abstract
There are many glucose-lowering agents used in patients with heart failure, showing mixed results, this study was conducted to determine the effect of liraglutide, a glucagon-like peptide-1 analogue, on the treatment of patients with heart failure. Patients from the FIGHT and LIVE trials were included, all overlapped data were summarized and described. No significant changes from baseline in left ventricular ejection fraction, N-terminal pro-B-type natriuretic peptide, hemoglobin A1c, heart rate, left ventricular end-systolic volume index, left ventricular end-diastolic volume index, and 6 min walk test were observed in FIGHT. In LIVE, liraglutide significantly decreased hemoglobin A1c and inceased 6 min walk test and increased heart rate and serious cardiac adverse events, and there were no statistical differences in left ventricular ejection fraction, N-terminal pro-B-type natriuretic peptide, left ventricular end-systolic volume index, and left ventricular end-diastolic volume index. In this study, we found that there is not enough reason to support the use of liraglutide in patients with heart failure, and importantly, the safety of liraglutide in this particular population remains uncertain. Enhanced recognition the risks and benefits of liraglutide would help guide therapeutic decisions in patients with heart failure.
Verbatim abstract via PubMed 32631360 ↗
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