# Prognostic Significance of Malnutrition Indices in ST-Elevation Myocardial Infarction: A Comparative Analysis of CONUT and PNI Scores After Primary PCI

**Authors:** Fatma Can, Gönül Zeren, Tülay Bayram Gürkan, Zeynep Ece Demirbaş

PMC · DOI: 10.3390/diagnostics16040573 · 2026-02-14

## TL;DR

This study compares two malnutrition scores, CONUT and PNI, to predict in-hospital mortality in patients with heart attacks treated with a specific procedure.

## Contribution

The study shows that the CONUT score is better than PNI at predicting mortality in STEMI patients after primary PCI.

## Key findings

- In-hospital mortality rate was 5.7% among 4599 STEMI patients.
- CONUT score showed better predictive performance than PNI for in-hospital mortality.
- Moderate-to-severe malnutrition was observed in 17–21% of patients using CONUT and 8–10% using PNI.

## Abstract

Background: The purpose of this study was to compare the prognostic value of Controlling Nutritional Status (CONUT) and Prognostic Nutritional Index (PNI) scores for predicting in-hospital mortality among patients who presented with ST-segment elevation myocardial infarction (STEMI) and received primary percutaneous coronary intervention (P-PCI). Methods: This retrospective cohort study comprised 4599 STEMI patients who received P-PCI. The primary outcome was described as in-hospital mortality. Multivariable logistic regression analysis was performed to determine the association between in-hospital mortality and CONUT and PNI scores. Model performance and goodness-of-fit measures were used for comparison. Results: In-hospital mortality rate was 5.7% (n = 261). Patients who died during the index hospitalization were older and more likely to have diabetes, prior myocardial infarction (MI), revascularization history, longer total ischemic time, no-reflow and reduced left ventricular ejection fraction (LVEF). According to body mass index (BMI) categories, moderate-to-severe malnutrition was observed in approximately 17–21% and 8–10% of patients according to the CONUT and PNI scores, respectively. Both CONUT and PNI scores were significantly associated with in-hospital mortality. However, the model incorporating CONUT demonstrated superior goodness of fit and higher discriminative performance compared with the model incorporating PNI. Conclusions: Among patients with STEMI, moderate-severe malnutrition was present in nearly 10% and 20% when evaluated using PNI and CONUT, respectively. The CONUT score demonstrated superior predictive performance for in-hospital mortality compared with PNI.

## Linked entities

- **Diseases:** myocardial infarction (MONDO:0005068), diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** NPPB (natriuretic peptide B) [NCBI Gene 4879] {aka BNP, Iso-ANP}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** -reflow phenomenon (MESH:D054318), ACS (MESH:D054058), sarcopenia (MESH:D055948), MIA (MESH:D007249), injury to (MESH:D014947), malignancy (MESH:D009369), DM (MESH:D003920), left bundle branch block (MESH:D002037), ischemic (MESH:D002545), overweight (MESH:D050177), Cardiovascular cachexia (MESH:D002100), chest pain (MESH:D002637), myocardial blush (MESH:D009202), obese (MESH:D009765), ST-Elevation Myocardial Infarction (MESH:D000072657), ischemia (MESH:D007511), atherosclerotic (MESH:D050197), Takotsubo syndrome (MESH:D054549), death (MESH:D003643), CONUT (MESH:D044342), gastrointestinal malabsorption (MESH:D008286), HT (MESH:D006973), myocardial ischemia (MESH:D017202), End-stage renal disease (MESH:D007676), infection (MESH:D007239), cardiovascular disease (MESH:D002318), MI (MESH:D009203), CAD (MESH:D003324), heart failure (MESH:D006333), underweight (MESH:D013851), Chronic (MESH:D002908), Coronary (MESH:D003323)
- **Chemicals:** P (MESH:D010758), aspirin (MESH:D001241), cholesterol (MESH:D002784), ACE-I (-), clopidogrel (MESH:D000077144), urea (MESH:D014508), gadolinium (MESH:D005682), glucose (MESH:D005947), Creatinine (MESH:D003404), heparin (MESH:D006493)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939604/full.md

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Source: https://tomesphere.com/paper/PMC12939604