Key result
In computational models of AF patients, incorporating interstitial collagen deposits significantly decreased amplitude and increased fractionation on electrograms compared to controls.
Why the study?
How interstitial collagen deposits and epicardium-endocardium electrical dissociation manifest on the electrogram remains unclear.
Does epicardium-endocardium electrical dissociation caused by interstitial collagen affect unipolar electrogram characteristics in computational models of atrial fibrillation?
Does epicardium-endocardium electrical dissociation caused by interstitial collagen affect unipolar electrogram characteristics in computational models of atrial fibrillation?
Computational modeling demonstrates that transmural electrical dissociation from fibrosis significantly alters EGM morphology, suggesting these characteristics could be combined with imaging to better select AF ablation targets.
May link interstitial collagen to fractionated EGMs in AF models; leaves open whether this informs ablation targets.
Myocardial structural remodeling leads to atrial fibrillation (AF). Interstitial collagen deposits remodel myocardium, causing disruption of electrical propagation between the endocardial and the epicardial layers, and affecting propagation within layers as well. How these changes manifest on the electrogram (EGM) is unclear. Here we investigate the consequences of epicardium- endocardium electrical dissociation on EGMs. Left atrial patient-specific bilayer computational models were constructed using MRI from AF patients (n = 11). Interstitial collagen was incorporated as microstructural discontinuities within layers and causing transmural dissociation in the high-fibrosis areas. The models where the fibrosis was not included were considered as controls. Changes in the unipolar EGM characteristics were computed. A propagation delay was observed between both layers. No monotonic linear relationship between control and fibrotic EGMs was found. With the collagen deposits, amplitude decreases and increased fractionation on EGMs were significant. EGM area also tended to become smaller, and duration and waveform asymmetry were affected. In conclusion, measurements of EGM morphology can be used together with clinical imaging data to distinguish between different substrate modifications, and better select ablation targets.
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Saha et al. (2019) studied Atrial fibrillation (n=11). Interstitial collagen (fibrosis model) vs. Models without fibrosis (controls) was evaluated on Changes in unipolar EGM characteristics. In computational models of AF patients, incorporating interstitial collagen deposits significantly decreased amplitude and increased fractionation on electrograms compared to controls.
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