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Computationally Modelling Cholesterol Metabolism and Atherosclerosis

Davies, Callum; Morgan, Amy E.; Mc Auley, Mark T.

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Authors

Callum Davies

Profile image of Amy Morgan

Dr Amy Morgan A.E.Morgan2@salford.ac.uk
Lecturer in Biomedical Science



Abstract

Cardiovascular disease (CVD) is the leading cause of death globally. The underlying pathological driver of CVD is atherosclerosis. The primary risk factor for atherosclerosis is elevated low-density lipoprotein cholesterol (LDL-C). Dysregulation of cholesterol metabolism is synonymous with a rise in LDL-C. Due to the complexity of cholesterol metabolism and atherosclerosis mathematical models are routinely used to explore their non-trivial dynamics. Mathematical modelling has generated a wealth of useful biological insights, which have deepened our understanding of these processes. To date however, no model has been developed which fully captures how whole-body cholesterol metabolism intersects with atherosclerosis. The main reason for this is one of scale. Whole body cholesterol metabolism is defined by macroscale physiological processes, while atherosclerosis operates mainly at a microscale. This work describes how a model of cholesterol metabolism was combined with a model of atherosclerotic plaque formation. This new model is capable of reproducing the output from its parent models. Using the new model, we demonstrate how this system can be utilized to identify interventions that lower LDL-C and abrogate plaque formation.

Citation

Davies, C., Morgan, A. E., & Mc Auley, M. T. (2023). Computationally Modelling Cholesterol Metabolism and Atherosclerosis. Biology, 12(8), 1133. https://doi.org/10.3390/biology12081133

Journal Article Type Article
Acceptance Date Aug 10, 2023
Online Publication Date Aug 14, 2023
Publication Date Aug 14, 2023
Deposit Date Aug 22, 2024
Publicly Available Date Sep 18, 2024
Journal Biology
Electronic ISSN 2079-7737
Publisher MDPI
Peer Reviewed Peer Reviewed
Volume 12
Issue 8
Pages 1133
DOI https://doi.org/10.3390/biology12081133
PMID 37627017

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