Document Type
Article
Publication Date
12-1-2022
Abstract
AIM: To evaluate the cardiovascular outcomes of glucagon-like peptide-1 receptor agonists (GLP1-RA) in patients with type 2 diabetes (T2DM) and chronic kidney disease (CKD).
MATERIALS AND METHODS: We searched PubMed, Ovid MEDLINE, CINAHL, and Web of Science databases for randomized controlled trials reporting event rates for a composite cardiovascular outcome of cardiovascular death, myocardial infarction, and stroke in patients with T2DM and CKD receiving GLP1-RA or placebo. Studies were restricted to those reporting specific event rates for patients with CKD separately from the overall population. We conducted a meta-analysis using a random-effects model. This meta-analysis was registered on PROSPERO (CRD42022320157).
RESULTS: A total of four studies comprising 7130 patients was included in our analysis. Four different GLP1-RA were assessed in a population with CKD defined as estimated glomerular filtration rate (eGFR)/min/1.73 m
CONCLUSIONS: Pooled analysis of clinical trials reporting separate cardiovascular events rates in patients with T2DM and CKD did not find GLP1-RA to be associated with a reduction in composite cardiovascular event rates. Select GLP1-RA may offer cardiovascular event reduction in patients with T2DM and CKD, but this does not appear to be a class effect. Use of GLP1-RA with demonstrated cardiovascular benefits should be preferred in patients with CKD and T2DM to further reduce cardiovascular risk.
Recommended Citation
Kelly, Michael; Lewis, Jelena; Rao, Hindu; Carter, Jessica; Portillo, Ivan; and Beuttler, Richard, "Effects of GLP-1 Receptor Agonists on Cardiovascular Outcomes in Patients With Type 2 Diabetes and Chronic Kidney Disease: A Systematic Review and Meta-Analysis" (2022). College of Pharmacy Faculty Papers. Paper 55.
https://jdc.jefferson.edu/pharmacyfp/55
Creative Commons License
This work is licensed under a Creative Commons Attribution-Noncommercial 4.0 License
PubMed ID
36271706
Language
English
Comments
This article is the author's final published version in Pharmacotherapy, Volume 42, Issue 12, December 2022, Pg. 921 - 928.
The published version is available at https://doi.org/10.1002/phar.2737. Copyright © 2022 The Authors.