# Trimetazidine and allopurinol for the prevention of Contrast-associated acute kidney injury in elective percutaneous coronary intervention: a randomized controlled trial

**Authors:** Nourhan Osama Ali, Naglaa Samir Bazan, Hatem Hossam Mowafy, Mohamed E.A. Abdelrahim, Hadeer S. Harb

PMC · DOI: 10.1007/s00228-025-03985-6 · 2026-01-22

## TL;DR

This study tested if adding trimetazidine and allopurinol to standard hydration could prevent kidney injury after a heart procedure, but found no significant benefit.

## Contribution

The study is the first to evaluate the TMZ–allopurinol combination for contrast-associated acute kidney injury prevention in elective PCI patients.

## Key findings

- The TMZ–allopurinol combination showed a non-significant trend toward reducing CA-AKI incidence.
- ACEF and Mehran scores had limited predictive value for CA-AKI in this patient population.
- SGLT2 and DPP-4 inhibitors were associated with smaller creatinine increases, suggesting potential nephroprotection.

## Abstract

Contrast-associated acute kidney injury (CA-AKI) is a significant concern following percutaneous coronary intervention (PCI). This study assessed whether adding trimetazidine (TMZ) or TMZ/allopurinol to standard hydration reduces CA-AKI among elective PCI patients.

129 patients undergoing elective PCI were randomized into three groups: Group 1 received (IV isotonic saline + TMZ + allopurinol), Group 2 received (IV isotonic saline + TMZ), and Group 3 (control) received (IV isotonic saline only). The primary outcome was the incidence of CA-AKI at 24- and 48-hour post-PCI. Risk was stratified using the Mehran and the Age, Creatinine, and Ejection Fraction (ACEF) scores.

Group 1 demonstrated a non-significant reduction in CA-AKI incidence compared with Groups 2 and 3 (24 h: 4.65%, 4.55%, and 9.52%; 48 h: 16.28%, 20.45%, and 28.57%; p > 0.05). All patients were classified as low–moderate risk by ACEF and Mehran scores, neither of which predicted CA-AKI. At 48 h, SGLT2 inhibitors users demonstrated a smaller rise in creatinine compared with non-users (–0.04 ± 0.158 mg/dL vs. 0.096 ± 0.237 mg/dL, p < 0.05), as did DPP-4 inhibitor users (–0.05 ± 0.217 mg/dL vs. +0.098 ± 0.237 mg/dL, p < 0.05). Diuretics were associated with greater increases (p < 0.05).

The TMZ–allopurinol combination showed a favorable but non-significant trend toward reducing CA-AKI, while ACEF and Mehran scores demonstrated limited predictive value. Improved risk-stratification tools and larger studies in higher-risk patients are needed. SGLT2 and DPP-4 inhibitors showed smaller creatinine increases, suggesting possible nephroprotection, but this remains exploratory.

## Linked entities

- **Chemicals:** trimetazidine (PubChem CID 21109), allopurinol (PubChem CID 135401907)
- **Diseases:** acute kidney injury (MONDO:0002492), heart disease (MONDO:0005267)

## Full-text entities

- **Genes:** SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}
- **Diseases:** gout (MESH:D006073), hyperuricemia (MESH:D033461), Hepatitis C (MESH:D019698), cardiogenic shock (MESH:D012770), acidosis (MESH:D000138), fibrosis (MESH:D005355), CKD (MESH:D012080), ischemic (MESH:D002545), fluid overload (MESH:D019190), acute coronary syndromes (MESH:D054058), pulmonary edema (MESH:D011654), type 2 diabetes mellitus (MESH:D003924), end-stage renal disease (MESH:D007676), DM (MESH:D003920), AKI (MESH:D058186), inflammation (MESH:D007249), Disease (MESH:D004194), left ventricular systolic dysfunction (MESH:D018487), heart failure (MESH:D006333), ACEF (MESH:D054144), CIN (MESH:D005119), renal insufficiency (MESH:D051437), injury (MESH:D014947), Hypotension (MESH:D007022), Diet in Renal Disease (MESH:D007674), anemia (MESH:D000740), ischemia (MESH:D007511), hepatic failure (MESH:D017093), cytotoxic (MESH:D064420)
- **Chemicals:** aspirin (MESH:D001241), lipids (MESH:D008055), Metformin (MESH:D008687), ACEF (-), Meglumine Ioxitalamate (MESH:C001694), ticagrelor (MESH:D000077486), fatty acid (MESH:D005227), aminoglycosides (MESH:D000617), Creatinine (MESH:D003404), Iohexol (MESH:D007472), amphotericin B (MESH:D000666), Allopurinol (MESH:D000493), glucose (MESH:D005947), bicarbonate (MESH:D001639), Urea (MESH:D014508), clopidogrel (MESH:D000077144), N-acetylcysteine (MESH:D000111), vitamin C (MESH:D001205), oxygen (MESH:D010100), cisplatin (MESH:D002945), Uric Acid (MESH:D014527), Ioxitalamate (MESH:C002587), sodium chloride (MESH:D012965), adenosine triphosphate (MESH:D000255), TMZ (MESH:D014292)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12823743/full.md

---
Source: https://tomesphere.com/paper/PMC12823743