Review of GLP-1 and GIP receptor agonists'expanding role covers their guideline-directed use across cardiovascular, kidney, and metabolic conditions with emerging evidence for dual agonism.
Key findingReview of GLP-1 and GIP receptor agonists'expanding role covers their guideline-directed use across
What the researchers found
Review of GLP-1 and GIP receptor agonists'expanding role covers their guideline-directed use across cardiovascular, kidney, and metabolic conditions with emerging evidence for dual agonism.
Why it matters
These findings have practical implications for the growing number of patients using peptide-based therapies.
The numbers in context
Review covers large clinical outcome trials establishing GLP-1 RAs as guideline-directed therapies for multiple CKM conditions.
How the study worked
Study methodology detailed in the full publication.
Who was studied
Patients with cardiovascular-kidney-metabolic syndrome across major clinical trials
What this study cannot tell us
Study limitations in the full publication.
How to read the evidence
Evidence level based on study design in publication.
When this study was published
Published in 2025.
The bigger picture
This study contributes to the expanding evidence for peptide therapeutics in clinical practice.
Questions still open
- What are the long-term implications?
- How do results compare to other evidence?
- What further research is needed?
Common questions
What does this mean for patients?
How reliable is this?
Read the original research
Role of Glucagon-Like Peptide-1 and Glucose-Dependent Insulinotropic Polypeptide/Glucagon-Like Peptide-1 Receptor Agonists in Management of Cardiovascular-Kidney-Metabolic (CKM) Conditions.
Cardiology clinics, 43(3), 415-432
Citation
Alicic, Radica Z; Neumiller, Joshua J. (2025). Role of Glucagon-Like Peptide-1 and Glucose-Dependent Insulinotropic Polypeptide/Glucagon-Like Peptide-1 Receptor Agonists in Management of Cardiovascular-Kidney-Metabolic (CKM) Conditions.. Cardiology clinics, 43(3), 415-432. https://doi.org/10.1016/j.ccl.2024.12.003