Renal effects of GLP-1 receptor agonists and tirzepatide in individuals with type 2 diabetes: seeds of a promising future.
Endocrine · 2024
Last updated 2026-05-28A review of studies found that tirzepatide, a dual GIP/GLP-1 drug, may help protect the kidneys in people with type 2 diabetes by lowering blood sugar, reducing body weight by up to 20%, improving insulin sensitivity, decreasing systolic blood pressure by about 8 mmHg, and lowering inflammation and triglycerides. While these effects suggest potential benefits for kidney health, more research is needed to confirm whether tirzepatide directly reduces kidney damage or improves long-term kidney outcomes.
AI summary of the abstract below.
| Journal | Endocrine, 2024 |
|---|---|
| Citations | 31 |
| Relative citation ratio | 6.36 |
| NIH percentile | 95 |
| Molecules | tirzepatide |
| Conditions studied | Type 2 Diabetes, Chronic Kidney Disease |
Abstract
PURPOSE: Chronic kidney disease (CKD) is one of the most common complications of type 2 diabetes (T2D), and CKD-related disability and mortality are increasing despite the recent advances in diabetes management. The dual GIP/GLP-1 receptor agonist tirzepatide is among the furthest developed multi-agonists for diabetes care and has so far displayed promising nephroprotective effects. This review aims to summarize the evidence regarding the nephroprotective effects of glucagon-like peptide-1 receptor agonists (GLP-1RA) and tirzepatide and the putative mechanisms underlying the favorable renal profile of tirzepatide.
METHODS: A comprehensive literature search was performed from inception to July 31st 2023 to select research papers addressing the renal effects of GLP-1RA and tirzepatide.
RESULTS: The pathogenesis of CKD in patients with T2D likely involves many contributors besides hyperglycemia, such as hypertension, obesity, insulin resistance and glomerular atherosclerosis, exerting kidney damage through metabolic, fibrotic, inflammatory, and hemodynamic mechanisms. Tirzepatide displayed an unprecedented glucose and body weight lowering potential, presenting also with the ability to increase insulin sensitivity, reduce systolic blood pressure and inflammation and ameliorate dyslipidemia, particularly by reducing triglycerides levels.
CONCLUSION: Tirzepatide is likely to counteract most of the pathogenetic factors contributing to CKD in T2D, potentially representing a step forward in incretin-based therapy towards nephroprotection. Further evidence is needed to understand its role in renal hemodynamics, fibrosis, cell damage and atherosclerosis, as well as to conclusively show reduction of hard renal outcomes.
Verbatim abstract via PubMed 38472620 ↗
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