# Effects of Contemporary Therapies on Cardiovascular and Renal Outcomes in Diabetic Kidney Disease: A Systematic Review of Randomized Controlled Trials (RCTs)

**Authors:** Wisam Bachar Al Sumodi, Muslim Sajjad, Sami Ullah Rana, Ghulam Ahmed, Aakash Hans, Waleed Mirani

PMC · DOI: 10.7759/cureus.95400 · Cureus · 2025-10-25

## TL;DR

This study reviews how new treatments like finerenone affect heart and kidney outcomes in diabetic kidney disease patients.

## Contribution

The study highlights finerenone's effectiveness in reducing cardiovascular and renal risks in diabetic kidney disease.

## Key findings

- Finerenone reduces composite cardiovascular events and renal outcomes in patients with type 2 diabetes and CKD.
- Renal benefits of finerenone are dose-dependent up to 20 mg daily, with hyperkalemia as a notable side effect.
- Finerenone's benefits extend to diverse subgroups, including those with stage 4 CKD and those on other therapies.

## Abstract

This systematic review evaluated the impact of contemporary therapies on cardiovascular (CV) and renal outcomes in patients with diabetic kidney disease (DKD), with a particular focus on finerenone as a novel nonsteroidal mineralocorticoid receptor antagonist. Across eight eligible studies involving more than 13,000 participants with type 2 diabetes and chronic kidney disease (CKD), finerenone consistently reduced the risk of composite CV events, including CV death, myocardial infarction, stroke, and hospitalization for heart failure, as well as composite renal outcomes such as kidney failure, sustained estimated glomerular filtration rate decline, or renal death. Subgroup analyses demonstrated that these benefits extended across diverse populations, including patients with stage 4 CKD, those stratified by age and sex, and individuals receiving diuretics, GLP-1 receptor agonists, or with baseline left ventricular hypertrophy. Importantly, the renal protective effects appeared dose-dependent up to 20 mg daily, with safety concerns primarily limited to an increased incidence of hyperkalemia, though discontinuation rates remained low. An earlier comparative trial of renin-angiotensin system inhibitors showed no significant differences between agents but highlighted tolerability advantages with angiotensin receptor blockers. Collectively, these findings reinforce the role of finerenone as an effective therapy for cardiorenal risk reduction in DKD, while also identifying areas for further research including advanced kidney disease, long-term renal preservation, and combination therapy strategies.

## Linked entities

- **Chemicals:** finerenone (PubChem CID 24993045)
- **Diseases:** diabetic kidney disease (MONDO:0005016), type 2 diabetes (MONDO:0005148), chronic kidney disease (MONDO:0005300), cardiovascular disease (MONDO:0004995), heart failure (MONDO:0005252), myocardial infarction (MONDO:0005068), stroke (MONDO:0005098)

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}
- **Diseases:** heart failure (MESH:D006333), left ventricular hypertrophy (MESH:D017379), kidney disease (MESH:D007674), 4 CKD (MESH:D051436), kidney failure (MESH:D051437), stroke (MESH:D020521), death (MESH:D003643), myocardial infarction (MESH:D009203), type 2 diabetes (MESH:D003924), hyperkalemia (MESH:D006947), DKD (MESH:D003928)
- **Chemicals:** angiotensin system inhibitors (-), finerenone (MESH:C576501)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12643440/full.md

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Source: https://tomesphere.com/paper/PMC12643440