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Glucagon-like peptide-1 receptor agonist in myocardial infarction and atherosclerotic cardiovascular disease risk reduction: a comprehensive meta-analysis of number needed to treat, efficacy and safety.

Tang, Ansel Shao Pin; Hsu, Jovan Teng Yuan; Chong, Sheena Kar Shuan; Quek, Jingxuan; Shek, Genevieve; Sulaimi, Farisah; Chan, Kai En; Anand, Vickram Vijay; Chong, Bryan; Mehta, Anurag; Toh, Sue-Anne; Muthiah, Mark; Dimitriadis, Georgios K; le Roux, Carel W; Chan, Mark Yan-Yee; Mamas, Mamas Andreas; Chin, Yip Han; Chew, Nicholas W S

Glucagon-like peptide-1 receptor agonist in myocardial infarction and atherosclerotic cardiovascular disease risk reduction: a comprehensive meta-analysis of number needed to treat, efficacy and safety. Thumbnail


Authors

Ansel Shao Pin Tang

Jovan Teng Yuan Hsu

Sheena Kar Shuan Chong

Jingxuan Quek

Genevieve Shek

Farisah Sulaimi

Kai En Chan

Vickram Vijay Anand

Bryan Chong

Anurag Mehta

Sue-Anne Toh

Mark Muthiah

Georgios K Dimitriadis

Carel W le Roux

Mark Yan-Yee Chan

Yip Han Chin

Nicholas W S Chew



Abstract

BackgroundGlucagon like peptide-1 receptor agonist (GLP-1RA) use in individuals with high atherosclerotic cardiovascular disease (ASCVD) risk reduces major adverse cardiovascular events (MACE). However, its clinical impact, in terms of numbers needed to treat (NNT), efficacy and safety profile in reducing the risk of myocardial infarction (MI) and the individual ASCVD constituents remain unclear.MethodsElectronic databases, Medline and Embase were reviewed for randomized trials from inception to 29 May 2025. Risk-reduction effect of GLP-1RA were pooled using pairwise meta-analysis with random-effects model. The primary outcome was MI, and secondary outcomes were the individual ASCVD constituents.Results109,846 patients from 25 unique studies were included. Over a follow-up duration of 3.48 ± 1.51 (1.55 to 5.47) years, GLP-1RA reduced the risk of total MI (RR: 0.86, p < 0.01), with numbers needed to benefit (NNTB) of 207 to prevent one event of MI. Higher body mass index was associated with greater MI risk reduction (β: -0.09, p = 0.03) in GLP-1RA users. GLP-1RA reduced cardiovascular mortality (RR: 0.87, p < 0.01, NNTB 170), MACE (RR: 0.87, p < 0.01, NNTB 67) and stroke (RR: 0.88, p < 0.01, NNTB 335) compared to placebo. GLP-1RA commonly resulted in gastrointestinal side-effects amongst other systems (RR: 1.55, p < 0.01, NNTH 9).ConclusionGLP-1RA reduced the risk of MI, stroke, cardiovascular mortality and MACE in a broad range of patients with and without T2DM and/or prior ASCVD, supporting its role in ASCVD prevention, especially in the cohort with high BMI.Trial registrationOpen Science Framework ( https://doi.org/10.17605/OSF.IO/7VXN5 ).

Citation

Tang, A. S. P., Hsu, J. T. Y., Chong, S. K. S., Quek, J., Shek, G., Sulaimi, F., Chan, K. E., Anand, V. V., Chong, B., Mehta, A., Toh, S.-A., Muthiah, M., Dimitriadis, G. K., le Roux, C. W., Chan, M. Y.-Y., Mamas, M. A., Chin, Y. H., & Chew, N. W. S. (2025). Glucagon-like peptide-1 receptor agonist in myocardial infarction and atherosclerotic cardiovascular disease risk reduction: a comprehensive meta-analysis of number needed to treat, efficacy and safety. Cardiovascular Diabetology, 24(1), 285. https://doi.org/10.1186/s12933-025-02840-3

Journal Article Type Review
Acceptance Date Jun 24, 2025
Online Publication Date Jul 12, 2025
Publication Date 2025
Deposit Date Jul 31, 2025
Publicly Available Date Jul 31, 2025
Journal Cardiovascular diabetology
Electronic ISSN 1475-2840
Publisher Springer Verlag
Peer Reviewed Peer Reviewed
Volume 24
Issue 1
Pages 285
DOI https://doi.org/10.1186/s12933-025-02840-3
Keywords GLP-1-receptor agonist, GLP-1RA, Myocardial Infarction, Stroke, Cardiovascular mortality, Cardiovascular disease, Numbers-needed-to-treat
Public URL https://keele-repository.worktribe.com/output/1328172
PMID 40652242

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