# Time-Varying Prognostic Impact of the Age×BUN/LVEF Index on Long-Term MACCE After ST-Elevation Myocardial Infarction

**Authors:** Seda Elcim Yildirim, Tarik Yildirim, Mehmet Tolga Hekim, Tuncay Kiris, Eyüp Avci

PMC · DOI: 10.3390/jcdd13030130 · Journal of Cardiovascular Development and Disease · 2026-03-10

## TL;DR

A new index combining age, blood urea nitrogen, and heart function helps predict long-term heart risks in patients who had a severe heart attack.

## Contribution

The AGEBUNeFR index offers dynamic and incremental prognostic information for STEMI patients beyond conventional models.

## Key findings

- The AGEBUNeFR index was independently associated with MACCE after multivariable adjustment.
- The index showed significant prognostic value in both early and late post-PCI periods.
- It provides a practical tool for long-term risk stratification after STEMI.

## Abstract

Background: Despite advances in reperfusion strategies, long-term major adverse cardiac and cerebrovascular events (MACCE) remain frequent after ST-elevation myocardial infarction (STEMI). Practical risk stratification tools applicable at presentation are therefore needed. We investigated the prognostic value of a simple composite index integrating age, blood urea nitrogen, and left ventricular ejection fraction (Age×BUN/LVEF) for predicting long-term MACCE in STEMI patients treated with primary percutaneous coronary intervention (PCI). Methods: This retrospective, single-center cohort study included 313 consecutive STEMI patients undergoing primary PCI between 2020 and 2024. The Age×BUN/LVEF (AGEBUNeFR) index was calculated using age and admission blood urea nitrogen values and left ventricular ejection fraction assessed during index hospitalization. The primary outcome was long-term MACCE, defined as a composite of all-cause mortality, recurrent myocardial infarction, repeat revascularization, stroke, and heart failure hospitalization. The median follow-up was 2.24 years (interquartile range 1.40–3.06). Results: During follow-up, 93 patients (29.7%) experienced MACCE. The AGEBUNeFR index was independently associated with MACCE after multivariable adjustment (adjusted HR 1.028 per unit increase, 95% CI 1.016–1.040; p < 0.001). Time-varying analyses demonstrated a dynamic prognostic effect, with significant associations in the early post-PCI period (p = 0.002) and a pronounced re-emergence of risk during late follow-up (>36 months; p < 0.001). Conclusions: The AGEBUNeFR index is a simple, readily available, and powerful predictor of long-term MACCE in STEMI patients undergoing primary PCI. By integrating age, renal/hemodynamic stress, and cardiac function, this composite index provides dynamic and incremental prognostic information beyond conventional clinical models, supporting its potential role as a practical tool for long-term risk stratification after STEMI.

## Linked entities

- **Diseases:** myocardial infarction (MONDO:0005068), heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, ACE (angiotensin I converting enzyme) [NCBI Gene 1636] {aka ACE1, CD143, DCP, DCP1}, PCSK9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 255738] {aka FH3, FHCL3, HCHOLA3, LDLCQ1, NARC-1, NARC1}, AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}
- **Diseases:** ventricular remodeling (MESH:D020257), inflammation (MESH:D007249), Thrombus (MESH:D013927), myocardial stunning (MESH:D017682), heart failure (MESH:D006333), hypertension (MESH:D006973), ischemic (MESH:D002545), Advanced (MESH:D020178), TIMI (MESH:D009203), cardiac and cerebrovascular (MESH:D002561), chronic obstructive pulmonary disease (MESH:D029424), frailty (MESH:D000073496), coronary occlusion (MESH:D054059), reperfusion damage (MESH:D015427), diabetes mellitus (MESH:D003920), ischemia (MESH:D007511), myocardial damage (MESH:D009202), coronary artery disease (MESH:D003324), ST-Elevation Myocardial Infarction (MESH:D000072657), MACCE (MESH:D002318), systemic (MESH:D015619), myocardial dysfunction (MESH:D006331), Lung Cancer Inflammation (MESH:D008175), death (MESH:D003643), renal hypoperfusion (MESH:D006030), infarct (MESH:D007238), peripheral artery disease (MESH:D058729), LAD (MESH:C535887), Stroke (MESH:D020521), dyslipidemia (MESH:D050171), acute coronary syndrome (MESH:D054058), injury to (MESH:D014947), hemodynamic impairment (MESH:D060825)
- **Chemicals:** glucose (MESH:D005947), Urea (MESH:D014508), ASA (MESH:D001241), creatinine (MESH:D003404), triglycerides (MESH:D014280), lipid (MESH:D008055), ezetimibe (MESH:D000069438), urea nitrogen (MESH:C530477), MRA (MESH:C502936), cholesterol (MESH:D002784), antithrombotic (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13026586/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC13026586/full.md

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Source: https://tomesphere.com/paper/PMC13026586