TY - UNPB
T1 - Identifying locations susceptible to micro-anatomical reentry using a spatial network representation of atrial fibre maps
AU - Falkenberg, Max
AU - Coleman, James A.
AU - Dobson, Sam
AU - Hickey, David
AU - Terrill, Louie
AU - Ciacci, Alberto
AU - Thomas, Belvin
AU - Peters, Nicholas S.
AU - Sau, Arunashis
AU - Ng, Fu Siong
AU - Zhao, Jichao
AU - Christensen, Kim
N1 - Publisher Copyright:
© 2019 Creative Commons.
PY - 2021/9/15
Y1 - 2021/9/15
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85081116587&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0267166
DO - 10.1371/journal.pone.0267166
M3 - Preprint
AN - SCOPUS:85081116587
SP - 1
EP - 22
BT - Identifying locations susceptible to micro-anatomical reentry using a spatial network representation of atrial fibre maps
PB - bioRxiv
ER -