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Wild type and K897T polymorphisms of the hERG gene: modeling the APD in Caucasians

The presented study aims to assess the possibility of simulating changes in cardiac cell electrophysiology due to K897T polymorphism in the Caucasian population. In the first part of the experiment, the parameters of the equations describing channel gating were fitted to the experimental data. Then,...

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Detalles Bibliográficos
Autores principales: Glinka, Anna, Polak, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Biomedical Informatics 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3523219/
https://www.ncbi.nlm.nih.gov/pubmed/23251039
http://dx.doi.org/10.6026/97320630081062
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author Glinka, Anna
Polak, Sebastian
author_facet Glinka, Anna
Polak, Sebastian
author_sort Glinka, Anna
collection PubMed
description The presented study aims to assess the possibility of simulating changes in cardiac cell electrophysiology due to K897T polymorphism in the Caucasian population. In the first part of the experiment, the parameters of the equations describing channel gating were fitted to the experimental data. Then, the action potentials of midmyocardial cells of 100 individuals were simulated in the in vitro - in vivo extrapolation system - ToxComp. Mean APD90 for the entire simulated population is 352.05 ms (SD = 21.69 ms). Mean APD90 for the 80 individuals with the WT version of the hERG gene and for the 20 K897T homo- and heterozygotes is respectively 349.08 ms (SD = 21.09 ms) and 363.95ms (SD = 20.41 ms). The ToxComp system can be useful in predicting the impact of genetic variability on drug triggered cardiac cell electrophysiology interference.
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spelling pubmed-35232192012-12-18 Wild type and K897T polymorphisms of the hERG gene: modeling the APD in Caucasians Glinka, Anna Polak, Sebastian Bioinformation Hypothesis The presented study aims to assess the possibility of simulating changes in cardiac cell electrophysiology due to K897T polymorphism in the Caucasian population. In the first part of the experiment, the parameters of the equations describing channel gating were fitted to the experimental data. Then, the action potentials of midmyocardial cells of 100 individuals were simulated in the in vitro - in vivo extrapolation system - ToxComp. Mean APD90 for the entire simulated population is 352.05 ms (SD = 21.69 ms). Mean APD90 for the 80 individuals with the WT version of the hERG gene and for the 20 K897T homo- and heterozygotes is respectively 349.08 ms (SD = 21.09 ms) and 363.95ms (SD = 20.41 ms). The ToxComp system can be useful in predicting the impact of genetic variability on drug triggered cardiac cell electrophysiology interference. Biomedical Informatics 2012-11-13 /pmc/articles/PMC3523219/ /pubmed/23251039 http://dx.doi.org/10.6026/97320630081062 Text en © 2012 Biomedical Informatics This is an open-access article, which permits unrestricted use, distribution, and reproduction in any medium, for non-commercial purposes, provided the original author and source are credited.
spellingShingle Hypothesis
Glinka, Anna
Polak, Sebastian
Wild type and K897T polymorphisms of the hERG gene: modeling the APD in Caucasians
title Wild type and K897T polymorphisms of the hERG gene: modeling the APD in Caucasians
title_full Wild type and K897T polymorphisms of the hERG gene: modeling the APD in Caucasians
title_fullStr Wild type and K897T polymorphisms of the hERG gene: modeling the APD in Caucasians
title_full_unstemmed Wild type and K897T polymorphisms of the hERG gene: modeling the APD in Caucasians
title_short Wild type and K897T polymorphisms of the hERG gene: modeling the APD in Caucasians
title_sort wild type and k897t polymorphisms of the herg gene: modeling the apd in caucasians
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3523219/
https://www.ncbi.nlm.nih.gov/pubmed/23251039
http://dx.doi.org/10.6026/97320630081062
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