Identifying locations susceptible to micro-anatomical reentry using a spatial network representation of atrial fibre maps

Max Falkenberg, James A. Coleman, Sam Dobson, David Hickey, Louie Terrill, Alberto Ciacci, Belvin Thomas, Nicholas S. Peters, Arunashis Sau, Fu Siong Ng, Jichao Zhao, Kim Christensen

Research output: Working paper/PreprintPreprint

Abstract (may include machine translation)

Micro-anatomical reentry has been identified as a potential driver of atrial fibrillation (AF). In this paper, we introduce a novel computational method which aims to identify which atrial regions are most susceptible to micro-reentry. The approach, which considers the structural basis for micro-reentry only, is based on the premise that the accumulation of electrically insulating interstitial fibrosis can be modelled by simulating percolation-like phenomena on spatial networks. Our results suggest that at high coupling, where micro-reentry is rare, the micro-reentrant substrate is highly clustered in areas where the atrial walls are thin and have convex wall morphology. However, as transverse connections between fibres are removed, mimicking the accumulation of interstitial fibrosis, the substrate becomes less spatially clustered, and the bias to forming in thin, convex regions of the atria is reduced. Comparing our algorithm on image-based models with and without atrial fibre structure, we find that strong longitudinal fibre coupling can suppress the micro-reentrant substrate, whereas regions with disordered fibre orientations have an enhanced risk of micro-reentry. We suggest that with further development, these methods may have future potential for patient-specific risk stratification, taking a longitudinal view of the development of the micro-reentrant substrate.

Original languageEnglish
PublisherbioRxiv
Pages1-22
DOIs
StatePublished - 15 Sep 2021
Externally publishedYes

Fingerprint

Dive into the research topics of 'Identifying locations susceptible to micro-anatomical reentry using a spatial network representation of atrial fibre maps'. Together they form a unique fingerprint.

Cite this