Global Myocardial Work-Derived Nomogram for Coronary Stenosis Assessment in Stable Coronary Artery Disease: Development and External Validation
<b>Background:</b> 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. <b>Methods:</b> 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. <b>Results:</b> 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. <b>Conclusions:</b> Our nomogram provides a non-invasive tool for preoperative risk stratification and optimizes the use of invasive diagnostics in stable CAD patients without RWMA.
Authors
- Lei Li (ORCID: https://orcid.org/0000-0001-8723-3461)
- Qianshan Ding (ORCID: https://orcid.org/0000-0002-9989-6876)
- Pingyang Zhang
- Wenfang Wu
- Jing Dong
- Miao Li
Institutions
- Nanjing Medical University (CN)
Publication Details
- Journal
- Diagnostics
- Published
- 2026-02-13
- DOI
- https://doi.org/10.3390/diagnostics16040570
- Primary Topic
- Cardiovascular Function and Risk Factors
- Type
- article
- Field-Weighted Citation Impact
- 0.00