Key result
GLP-1 and dual agonists linked to ~53% lower major events in obese dialysis patients.
Why the study?
GLP-1 receptor agonists reduce weight and improve cardiovascular outcomes in patients with obesity regardless of diabetes status, but little is known about their cardiovascular effects in patients with obesity and end-stage CKD on dialysis.
Does the use of GLP-1 receptor agonists and dual agonists reduce the composite of all-cause mortality, myocardial infarction, or stroke in non-diabetic adults with overweight or obesity and dialysis-dependent end-stage chronic kidney disease?
Cohort (n=3,136)
Yes
Does the use of GLP-1 receptor agonists and dual agonists reduce the composite of all-cause mortality, myocardial infarction, or stroke in non-diabetic adults with overweight or obesity and dialysis-dependent end-stage chronic kidney disease?
In non-diabetic patients with overweight or obesity and dialysis-dependent CKD, GLP-1 receptor agonists and dual agonists are associated with significantly lower rates of major adverse cardiovascular events and all-cause mortality.
Introduction Glucagon-like peptide-1 (GLP-1) receptor agonists have demonstrated weight reduction and improvement in cardiovascular outcomes in patients with obesity regardless of the presence of diabetes. However, little is known about its effects among patients with end-stage chronic kidney disease (CKD). This study aims to determine whether the administration of these analogs in patients with obesity and CKD on dialysis results in a reduction of cardiovascular events. Objective To evaluate, utilizing real-world data, whether the use of GLP-1 receptor agonists and dual agonists is associated with a reduction in cardiovascular events and all-cause mortality in obese patients with end-stage CKD on dialysis. METHODOLOGY: We conducted a retrospective cohort analysis using the TriNetX Global Health Research Network via anonymized electronic medical records. We identified adult patients (≥18 years) with overweight or obesity (Body Mass Index (BMI) ≥ 27 kg/m²) and dialysis-dependent CKD, categorized into those treated with (exposure group) or without (control group) GLP-1 receptor agonists and dual agonists. Patients with diabetes, priorbariatric surgery or kidney transplantation were excluded. . Users of GLP-1 and dual agonists were matched to the reference cohort (non-users) using propensity score matching. The primary outcome was a composite of all-cause mortality, myocardial infarction (MI), or stroke. Results After propensity score matching, the final cohort comprised 3,136 patients monitored over median a 10-year follow-up period. The use of GLP-1 and dual agonists was associated with reduction in the of composite of death, MI, or stroke) compared to the reference group (HR 0.47; 95% CI 0.39–0.57). In secondary analyses, the benefits were statistically significant for all-cause mortality (HR 0.34; 95% CI 0.26–0.43) and MI (HR 0.56; 95% CI 0.38–0.82) componentes, but not for. stroke (HR 0.94; 95% CI 0.61–1.43). Conclusion In obese patients with CKD on dialysis, the use of GLP-1 and dual agonists was associated with a reduction in major cardiovascular events and all-cause mortality. These findings suggest that these therapies may provide substantial cardioprotective benefits in this high-risk population. Randomzied studies to confirm our findings in this populaiton are warranted.
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Prado et al. (2026) conducted a cohort in Overweight or obesity and dialysis-dependent end-stage chronic kidney disease (n=3,136). GLP-1 receptor agonists and dual agonists vs. Non-users (reference cohort) was evaluated on Composite of all-cause mortality, myocardial infarction (MI), or stroke (HR 0.47, 95% CI 0.39–0.57). GLP-1 and dual agonist use was associated with a reduced composite of all-cause mortality, MI, or stroke compared to non-use in obese patients on dialysis (HR 0.47; 95% CI 0.39–0.57).
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