# Prognostic value of cardiac magnetic resonance–derived global longitudinal strain in LGE-negative dilated cardiomyopathy

**Authors:** Tian-Yue Zhang, Tian Lan, Ling-Li Wang, Yu-Cong Zheng, Xin-Yi Feng, Fei-Yao Wang, Fan Zhang, Hua-Yan Xu, Xi Liu, Zhi Yang, Rui Li

PMC · DOI: 10.1371/journal.pone.0345077 · PLOS One · 2026-03-27

## TL;DR

This study shows that global longitudinal strain from cardiac MRI improves risk prediction for sudden cardiac death in patients with a specific type of heart disease.

## Contribution

The study demonstrates that GLS is a novel independent predictor of sudden cardiac death in LGE-negative dilated cardiomyopathy.

## Key findings

- GLS remained significant in predicting sudden cardiac death in patients with LVEF <20%.
- A model combining GLS and LVEF outperformed LVEF alone in predicting sudden cardiac death.
- Adding age and NYHA classification further improved the model's performance.

## Abstract

Dilated cardiomyopathy (DCM) is a major cause of heart failure and sudden cardiac death (SCD), with a 5-year survival rate of approximately 45%–50%. Current risk stratification is predominantly dependent on left ventricular ejection fraction (LVEF), which has limited sensitivity and specificity. Hence, more effective biomarkers should be used in late gadolinium enhancement (LGE)-negative patients.

A total of 378 consecutive patients with LGE-negative DCM were enrolled from four hospitals between December 2016 and December 2022. Cardiac magnetic resonance imaging-derived strain parameters (global radial strain, global circumferential strain, and global longitudinal strain [GLS]) were assessed against the primary (SCD and related events) and secondary (heart failure, appropriate implantable cardioverter-defibrillator therapy) endpoints. Internal validation was performed using stratified bootstrap resampling with Harrell’s optimism correction to report the optimism-corrected C-index. Data were accessed for research purposes from 15/06/2023–30/12/2023, and all records were de-identified prior to analysis.

Over a median follow-up of 59.78 months, 35 (9.26%) and 72 (19.0%) patients presented with the primary and secondary endpoints, respectively. Based on the multivariate Cox analysis, GLS, LVEF, and age were independent prognostic factors. However, only GLS (HR = 1.37; P = 0.041) remained significant in the LVEF <20% subgroup. A model integrating GLS and LVEF had a better discrimination ability for SCD than LVEF strata alone (apparent C-index 0.756 vs 0.714, P < 0.001). This advantage persisted after bootstrap internal validation (B = 1000; optimism-corrected C-index 0.754 vs 0.711, Holm adjusted P = 0.048). Further inclusion of age and New York Heart Association (NYHA) classification enhanced the model’s performance (model 4): apparent C-index 0.801; optimism-corrected C-index 0.785).

GLS is an independent predictor of SCD-related events in LGE-negative DCM. Incorporating GLS with conventional indicators such as age, NYHA classification, and LVEF significantly enhances prognostic discrimination and model robustness, indicating potential value for future clinical risk stratification.

## Linked entities

- **Diseases:** dilated cardiomyopathy (MONDO:0005021), heart failure (MONDO:0005252), sudden cardiac death (MONDO:0007264)

## Full-text entities

- **Diseases:** SCD (MESH:D016757), arrhythmic (OMIM:212500), acute myocardial injury (MESH:D056486), myocardial strain (MESH:D013180), ventricular fibrillation (MESH:D014693), fibrosis (MESH:D005355), hypertension (MESH:D006973), heart failure (MESH:D006333), mitral insufficiency (MESH:D008944), respiratory (MESH:D012131), valvular heart disease (MESH:D006349), LV dilation (MESH:D018487), inflammation (MESH:D007249), ventricular tachycardia (MESH:D017180), VAs (MESH:D001145), LGE (MESH:C564835), myocardial dysfunction (MESH:D006331), CMR (MESH:C564543), deaths (MESH:D003643), left bundle branch block (MESH:D002037), VA (MESH:C563443), myocarditis (MESH:D009205), stenosis (MESH:D003251), DCM (MESH:D002311), cardiomyopathies (MESH:D009202), tachyarrhythmia (MESH:D013610), ICD (MESH:D057873), microvascular dysfunction (MESH:D017566), coronary artery disease (MESH:D003324), cardiac arrest (MESH:D006323)
- **Chemicals:** implantable (-), gadolinium (MESH:D005682)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13028522/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC13028522/full.md

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Source: https://tomesphere.com/paper/PMC13028522