# Global Myocardial Work-Derived Nomogram for Coronary Stenosis Assessment in Stable Coronary Artery Disease: Development and External Validation

**Authors:** Miao Li, Wenfang Wu, Lin Li, Qianshan Ding, Jing Dong, Pingyang Zhang

PMC · DOI: 10.3390/diagnostics16040570 · Diagnostics · 2026-02-13

## TL;DR

This study creates and validates a non-invasive tool using heart function data to identify significant coronary blockages in patients with stable heart disease.

## Contribution

A novel nomogram combining global myocardial work efficiency and clinical biomarkers is developed and validated for coronary stenosis assessment.

## Key findings

- The nomogram achieved high discrimination in both training and validation sets (AUC 0.916 and 0.911, respectively).
- The model showed good calibration with low mean absolute error in both training and validation sets.
- Decision curve analysis confirmed the clinical utility of the nomogram across all probability thresholds.

## Abstract

Background: Non-invasive identification of coronary stenosis in stable coronary artery disease (CAD) patients lacking regional wall motion abnormalities (RWMA) remains challenging. This study aimed to develop and validate a myocardial work-derived nomogram for predicting significant coronary stenosis in these patients. Methods: In this retrospective study, 181 consecutive patients with angiographically confirmed CAD, preserved LVEF (≥55%), and no resting wall motion abnormalities were enrolled. Global myocardial work efficiency (GWE) was assessed using echocardiographic pressure–strain loop analysis. A multivariable-derived nomogram incorporating GWE and clinical biomarkers was developed and externally validated for predicting severe coronary stenosis. Results: The nomogram incorporating GWE, lipoprotein-associated phospholipase A2 (LP-PLA2), N-terminal pro brain natriuretic peptide (NT-proBNP), and serum creatinine (Scr) demonstrated favorable discrimination in both the training set (AUC 0.916, 95% CI 0.866–0.952) and validation set (AUC 0.911, 95% CI 0.853–0.951), with good calibration (mean absolute error: 1.9% vs 3.2% in training vs validation, respectively). Decision curve analysis confirmed clinical utility across all probability thresholds. Conclusions: Our nomogram provides a non-invasive tool for preoperative risk stratification and optimizes the use of invasive diagnostics in stable CAD patients without RWMA.

## Linked entities

- **Diseases:** coronary artery disease (MONDO:0005010)

## Full-text entities

- **Genes:** PLA2G7 (phospholipase A2 group VII) [NCBI Gene 7941] {aka LDL-PLA2, LP-PLA2, PAFAD, PAFAH}, ACE (angiotensin I converting enzyme) [NCBI Gene 1636] {aka ACE1, CD143, DCP, DCP1}, APOA1 (apolipoprotein A1) [NCBI Gene 335] {aka AMYLD3, HPALP2, apo(a)}, CCS (copper chaperone for superoxide dismutase) [NCBI Gene 9973], LPA (lipoprotein(a)) [NCBI Gene 4018] {aka AK38, APOA, LP}, AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}, APOB (apolipoprotein B) [NCBI Gene 338] {aka FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48}
- **Diseases:** inflammation (MESH:D007249), injury to (MESH:D014947), hyperlipidemia (MESH:D006949), LVOT obstruction (MESH:D000092242), coronary lesion (MESH:D003327), acute coronary syndrome (MESH:D054058), RWMA (MESH:D009041), diabetes mellitus (MESH:D003920), ischemic (MESH:D002545), valvular disease (MESH:D006349), angina (MESH:D000787), aortic stenosis (MESH:D001024), arrhythmia (MESH:D001145), chest pain (MESH:D002637), cardiomyopathy (MESH:D009202), Stroke (MESH:D020521), ischemia (MESH:D007511), stenosis (MESH:D003251), triple-vessel disease (MESH:C536008), Coronary Stenosis (MESH:D023921), hypertension (MESH:D006973), myocardial infarction (MESH:D009203), obstructive lesions (MESH:D008173), myocardial dysfunction (MESH:D006331), CAD (MESH:D003324), mechanical dysfunction (MESH:D041781)
- **Chemicals:** oxygen (MESH:D010100), TG (MESH:D014280), cholesterol (MESH:D002784), blood glucose (MESH:D001786), DCA (-), 18F-FDG (MESH:D019788), glucose (MESH:D005947), creatinine (MESH:D003404), calcium (MESH:D002118)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12939228/full.md

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Source: https://tomesphere.com/paper/PMC12939228