Constructing human atrial electrophysiological models mimicking a patient-specific cell group
Patient-specific modelling aims to produce computational models of human physiology tailored to a specific patient. In line with this, we construct multiple human atrial electrophysiological models mimicking the behaviour of single atrial myocytes extracted from a homogeneous patient group. We study...
Main Authors: | , , , , |
---|---|
Format: | Conference item |
Published: |
Institute of Electrical and Electronics Engineers
2015
|
_version_ | 1797070547984580608 |
---|---|
author | Muszkiewicz, A Bueno-Orovio, A Liu, X Casadei, B Rodriguez, B |
author_facet | Muszkiewicz, A Bueno-Orovio, A Liu, X Casadei, B Rodriguez, B |
author_sort | Muszkiewicz, A |
collection | OXFORD |
description | Patient-specific modelling aims to produce computational models of human physiology tailored to a specific patient. In line with this, we construct multiple human atrial electrophysiological models mimicking the behaviour of single atrial myocytes extracted from a homogeneous patient group. We study cells with the action potential duration being 2-3 times lower than in human atrial electrophysiological models. Assuming such a difference can be rationalized by altering the values of ionic conductances, we generated 15000 models by simultaneously varying conductance values of the most important currents affecting the action potential (AP). We paced the models at different frequencies and conditions, probing the importance of ion concentrations and stimulus strength, and kept the models producing AP biomarkers consistent with experiments. We discovered that both the ionic conductances and external factors play a critical role in producing biomarker values consistent with experiments. By mimicking experimental conditions, we generated 604 models fully covering the experimental range of AP biomarkers. In conclusion, both the ionic conductances and external factors are vital in tailoring single-cell electrophysiological models to a narrow patient group. This has implications in understanding the propensity of subgroups of the total population to disease conditions. |
first_indexed | 2024-03-06T22:40:25Z |
format | Conference item |
id | oxford-uuid:5b5ad72d-4805-4aaa-9650-bc9cc2665780 |
institution | University of Oxford |
last_indexed | 2024-03-06T22:40:25Z |
publishDate | 2015 |
publisher | Institute of Electrical and Electronics Engineers |
record_format | dspace |
spelling | oxford-uuid:5b5ad72d-4805-4aaa-9650-bc9cc26657802022-03-26T17:21:35ZConstructing human atrial electrophysiological models mimicking a patient-specific cell groupConference itemhttp://purl.org/coar/resource_type/c_5794uuid:5b5ad72d-4805-4aaa-9650-bc9cc2665780Symplectic Elements at OxfordInstitute of Electrical and Electronics Engineers2015Muszkiewicz, ABueno-Orovio, ALiu, XCasadei, BRodriguez, BPatient-specific modelling aims to produce computational models of human physiology tailored to a specific patient. In line with this, we construct multiple human atrial electrophysiological models mimicking the behaviour of single atrial myocytes extracted from a homogeneous patient group. We study cells with the action potential duration being 2-3 times lower than in human atrial electrophysiological models. Assuming such a difference can be rationalized by altering the values of ionic conductances, we generated 15000 models by simultaneously varying conductance values of the most important currents affecting the action potential (AP). We paced the models at different frequencies and conditions, probing the importance of ion concentrations and stimulus strength, and kept the models producing AP biomarkers consistent with experiments. We discovered that both the ionic conductances and external factors play a critical role in producing biomarker values consistent with experiments. By mimicking experimental conditions, we generated 604 models fully covering the experimental range of AP biomarkers. In conclusion, both the ionic conductances and external factors are vital in tailoring single-cell electrophysiological models to a narrow patient group. This has implications in understanding the propensity of subgroups of the total population to disease conditions. |
spellingShingle | Muszkiewicz, A Bueno-Orovio, A Liu, X Casadei, B Rodriguez, B Constructing human atrial electrophysiological models mimicking a patient-specific cell group |
title | Constructing human atrial electrophysiological models mimicking a patient-specific cell group |
title_full | Constructing human atrial electrophysiological models mimicking a patient-specific cell group |
title_fullStr | Constructing human atrial electrophysiological models mimicking a patient-specific cell group |
title_full_unstemmed | Constructing human atrial electrophysiological models mimicking a patient-specific cell group |
title_short | Constructing human atrial electrophysiological models mimicking a patient-specific cell group |
title_sort | constructing human atrial electrophysiological models mimicking a patient specific cell group |
work_keys_str_mv | AT muszkiewicza constructinghumanatrialelectrophysiologicalmodelsmimickingapatientspecificcellgroup AT buenoorovioa constructinghumanatrialelectrophysiologicalmodelsmimickingapatientspecificcellgroup AT liux constructinghumanatrialelectrophysiologicalmodelsmimickingapatientspecificcellgroup AT casadeib constructinghumanatrialelectrophysiologicalmodelsmimickingapatientspecificcellgroup AT rodriguezb constructinghumanatrialelectrophysiologicalmodelsmimickingapatientspecificcellgroup |