High resolution, 3D isotropic late gadolinium enhanced imaging for the quantification of left atrial fibrosis and post-ablation scarring
Authors
- Maximilian Fenski
- Richard Hickstein
- Leo Dyke Krüger
- Clemens Ammann
- Thomas Hadler
- Karl Kunze
- Michaela Schmidt
- René M. Botnar
- Claudia Prieto
- André Rudolph
- Marcel Prothmann
- Michael Wiedemann
- Thomas H. Grandy
- Jeanette Schulz-Menger
Journal
- European Heart Journal - Imaging Methods and Practice
Citation
- Eur Heart J Imaging Methods Pract 4 (1): qyag100
Abstract
AIMS: Left atrial (LA) myopathy is a key driver of atrial fibrillation (AF) development and progression. Late gadolinium enhancement (LGE) cardiovascular magnetic resonance enables non-invasive quantification of LA fibrosis, a hallmark of atrial myopathy. However, conventional LGE sequences lack sufficient spatial resolution to accurately depict the thin atrial wall, and reference data in healthy cohorts are scarce. This study aimed to evaluate a high-resolution isotropic 3D LGE Dixon sequence for assessing LA fibrosis in healthy controls and AF patients. METHODS AND RESULTS: In this prospective study, 40 ablation-naïve AF patients (21 paroxysmal, 19 persistent) and 20 healthy controls underwent isotropic (1.3 mm3) 3D whole-heart LGE imaging. Segmentation was successfully performed using CemrgApp in all participants. A setup-specific threshold for fibrosis detection was defined as an image-intensity ratio (IIR) > 1.34 (mean + 2SD of healthy controls) and validated against pre-procedural electroanatomical mapping (EAM) and follow-up imaging at six months post ablation. At baseline, total LA enhancement was higher in persistent than paroxysmal AF (3.65% [1.84–7.16] vs. 1.16% [0.43–2.27]; P = 0.044) and controls (1.25% [0.65–1.75]; P = 0.041). No significant correlation was observed between total LGE-derived fibrosis and bipolar low-voltage area (ρ = −0.03, P = 0.87), though point-by-point analysis showed a weak negative correlation (ρ = −0.05, P < 0.001). In patients with sinus rhythm at follow-up, total fibrosis increased from 1.68% [0.64–6.51] to 6.30% [2.53–12.28]; P < 0.001, driven by peri-ablational scar formation, with no change in remote myocardium. Intra-reader correlation for LA-LGE was excellent: ICC 0.99 (95% CI 0.95–0.99). CONCLUSION: High resolution isotropic 3D LA-LGE enables robust detection of ablation-induced scarring and biologically plausible fibrosis differences between AF stages. However, its correlation with bipolar voltage mapping remains limited, suggesting that LGE and EAM provide complementary information on atrial myopathy.