# Coronary angiography–derived index of microcirculatory resistance associated with contrast-induced acute kidney injury in patients with STEMI

**Authors:** Sifang Zhong, Jinyang Lu, Kaiyue Gong, Yixuan Wu, Zishuang Dong, Yuan Lu

PMC · DOI: 10.3389/fcvm.2025.1541208 · Frontiers in Cardiovascular Medicine · 2025-05-01

## TL;DR

This study finds that a measure of coronary microcirculatory dysfunction is linked to a higher risk of kidney injury after heart procedures in STEMI patients.

## Contribution

The study identifies caIMR as an independent predictor and improves risk models for contrast-induced acute kidney injury in STEMI patients.

## Key findings

- caIMR is an independent predictor of CI-AKI (OR = 1.072, 95% CI: 1.051–1.094).
- RCS analysis shows a linear dose-response relationship between caIMR and CI-AKI.
- Adding caIMR improves risk prediction (NRI = 0.721, IDI = 0.102).

## Abstract

More than half of ST-segment elevation myocardial infarction (STEMI) patients have coronary microcirculatory dysfunction (CMD) after percutaneous coronary intervention (PCI). This study aimed to explore the role of CMD in the occurrence of contrast-induced acute kidney injury (CI-AKI) in patients with STEMI.

This was a single-centre retrospective clinical observational study. Coronary angiography–derived index of microcirculatory resistance (caIMR) was measured and used to assess CMD. Regression analysis was used to identify risk factors for CI-AKI. Restricted cubic splines (RCS) was employed to examine the dose-response relationship between caIMR and CI-AKI. The predictive accuracy of the models was assessed with net reclassification index (NRI), and integrated discrimination improvement (IDI).

This study included 745 patients, the incidence of CI-AKI was 10.6% (79/745). Multivariate logistic regression identified caIMR (OR = 1.072, 95% CI: 1.051–1.094) as an independent predictor of CI-AKI. RCS analysis indicated a linear dose-response relationship between caIMR and CI-AKI. Receiver operating characteristic (ROC) analysis demonstrated that the areas under the curve for caIMR was 0.725, the optimal cutoff value was 25.95 U. Integration of caIMR could significantly improve the risk model for CI-AKI in STEMI patients (NRI = 0.721, IDI = 0.102, P < 0.001).

Elevated caIMR is an independent risk factor for the development of CI-AKI after PCI in STEMI patients. Integrating caIMR significantly improves the risk model for CI-AKI.

## Linked entities

- **Diseases:** ST-segment elevation myocardial infarction (MONDO:0041656)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, TNNT1 (troponin T1, slow skeletal type) [NCBI Gene 7138] {aka ANM, NEM5, STNT, TNT, TNTS}
- **Diseases:** CI-AKI (MESH:D058186), endothelial dysfunction (MESH:D014652), cardiovascular diseases (MESH:D002318), hyperemia (MESH:D006940), ST-segment elevation myocardial infarction (MESH:D000072657), CKD (MESH:D051436), myocardial reperfusion injury (MESH:D015428), hematologic disorders (MESH:D006402), CMD (MESH:D003327), coronary (MESH:D003323), inflammatory (MESH:D007249), kidney dysfunction (MESH:D007674), autoimmune diseases (MESH:D001327), microvascular dysfunction (MESH:D017566), TIMI (MESH:D009203), myocardial damage (MESH:D009202), malignancy (MESH:D009369), dysfunction (MESH:D006331), infarct (MESH:D007238), diabetes (MESH:D003920), chronic renal failure (MESH:D007676), pulmonary infection (MESH:D012141)
- **Chemicals:** aspirin (MESH:D001241), FBG (-), Nicorandil (MESH:D020108), creatinine (MESH:D003404), adenosine (MESH:D000241), glucose (MESH:D005947), nitrates (MESH:D009566)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12078307/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12078307/full.md

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Source: https://tomesphere.com/paper/PMC12078307