# Short- and Middle-Term Nephroprotective and Cardioprotective Effects of Pentoxifylline in Patients with Diabetic Nephropathy: A Randomized Controlled Trial

**Authors:** Oliva Mejía-Rodríguez, Marcela Ávila-Díaz, Carmen Prado-Uribe, María Eugenia Galván-Plata, Helios Vega Gómez, Cleto Álvarez-Aguilar, Miguel Angel Cuevas-Budhart, Ramón Paniagua

PMC · DOI: 10.3390/medsci14010026 · Medical Sciences · 2026-01-06

## TL;DR

Pentoxifylline helps protect both the kidneys and heart in diabetic patients with advanced kidney disease.

## Contribution

This study is the first to demonstrate combined nephroprotective and cardioprotective effects of pentoxifylline in diabetic nephropathy patients.

## Key findings

- Pentoxifylline significantly reduced microalbuminuria and improved kidney function over 12 months.
- Pentoxifylline decreased left ventricular mass index, indicating heart protection.
- The drug was well-tolerated with no significant adverse events.

## Abstract

Background/Objectives. Pentoxifylline (PTF) is an effective treatment to delay the progress of Diabetic Nephropathy; it also has beneficial effects on heart failure, two closely related clinical conditions. However, the simultaneous Nephroprotective and Cardioprotective effects of PTF have not been appropriately analyzed. The objective of this study was to analyze if both effects occur together in Diabetic patients. Material and Methods. A Randomized Controlled Trial was performed to compare Placebo (P-G) vs. PTF (400 mg/8 h) (PTF-G) in patients with CKD stages III–IV (KDIGO) due to Diabetic Nephropathy. Creatinine-Cystatin C-based Estimated Glomerular Filtration Rate (eGFRCysCCr) and Microalbuminuria were evaluated at baseline, six, and twelve months. Echocardiographic assessment of heart morphology and function was performed. Results. Ninety-three patients were available for the final analysis, 52 in the PTF group and 41 in the P group. There were no differences in clinical and biochemical parameters between groups at baseline. At 6 months, microalbuminuria changed 27.96 ± 43.06 in P-G and −30.27 ± 41.48 mg/24 h in PTF-G (p < 0.001), eGFRCysCCr changed −1.55 ± 7.10 in P-G and 1.40 ± 7.28 mL/min/1.73 m2 in PTF-G (p = 0.083), and left ventricular mass index (LVMI) changed 10.86 ± 16.40 in P-G and −2.71 ± 19.52 g/m2 in PTF-G (p = 0.001). At 12 months, microalbuminuria changed 24.10 ± 43.28 in P-G and −43.18 ± 52.13 mg/24 h in PTF-G (p < 0.001), eGFRCysCCr changed −6.55 ± 10.18 in P-G and 0.98 ± 8.17 mL/min/1.73 m2 in PTF-G (p = 0.008), and LVMI changed 20.79 ± 20.06 in P-G and −0.82 ± 25.95 g/m2 in PTF-G (p = 0.028). No significant adverse events occurred in any group. Conclusions. Pentoxifylline is a safe and effective treatment with combined Nephroprotective and Cardioprotective effects in advanced diabetic nephropathy.

## Linked entities

- **Chemicals:** Pentoxifylline (PubChem CID 4740)
- **Diseases:** Diabetic Nephropathy (MONDO:0005016), heart failure (MONDO:0005252)

## Full-text entities

- **Diseases:** Diabetic Nephropathy (MESH:D003928), CKD (MESH:D012080), Diabetic (MESH:D003920), heart failure (MESH:D006333)
- **Chemicals:** microalbuminuria (-), PTF (MESH:D010431), Creatinine (MESH:D003404), P (MESH:D010758)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12821668/full.md

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Source: https://tomesphere.com/paper/PMC12821668