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International Multisite Study of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Drug Proarrhythmic Potential Assessment

To assess the utility of human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) as an in vitro proarrhythmia model, we evaluated the concentration dependence and sources of variability of electrophysiologic responses to 28 drugs linked to low, intermediate, and high torsades de point...

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Autores principales: Blinova, Ksenia, Dang, Qianyu, Millard, Daniel, Smith, Godfrey, Pierson, Jennifer, Guo, Liang, Brock, Mathew, Lu, Hua Rong, Kraushaar, Udo, Zeng, Haoyu, Shi, Hong, Zhang, Xiaoyu, Sawada, Kohei, Osada, Tomoharu, Kanda, Yasunari, Sekino, Yuko, Pang, Li, Feaster, Tromondae K., Kettenhofen, Ralf, Stockbridge, Norman, Strauss, David G., Gintant, Gary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6226030/
https://www.ncbi.nlm.nih.gov/pubmed/30257217
http://dx.doi.org/10.1016/j.celrep.2018.08.079
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author Blinova, Ksenia
Dang, Qianyu
Millard, Daniel
Smith, Godfrey
Pierson, Jennifer
Guo, Liang
Brock, Mathew
Lu, Hua Rong
Kraushaar, Udo
Zeng, Haoyu
Shi, Hong
Zhang, Xiaoyu
Sawada, Kohei
Osada, Tomoharu
Kanda, Yasunari
Sekino, Yuko
Pang, Li
Feaster, Tromondae K.
Kettenhofen, Ralf
Stockbridge, Norman
Strauss, David G.
Gintant, Gary
author_facet Blinova, Ksenia
Dang, Qianyu
Millard, Daniel
Smith, Godfrey
Pierson, Jennifer
Guo, Liang
Brock, Mathew
Lu, Hua Rong
Kraushaar, Udo
Zeng, Haoyu
Shi, Hong
Zhang, Xiaoyu
Sawada, Kohei
Osada, Tomoharu
Kanda, Yasunari
Sekino, Yuko
Pang, Li
Feaster, Tromondae K.
Kettenhofen, Ralf
Stockbridge, Norman
Strauss, David G.
Gintant, Gary
author_sort Blinova, Ksenia
collection PubMed
description To assess the utility of human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) as an in vitro proarrhythmia model, we evaluated the concentration dependence and sources of variability of electrophysiologic responses to 28 drugs linked to low, intermediate, and high torsades de pointes (TdP) risk categories using two commercial cell lines and standardized protocols in a blinded multisite study using multielectrode array or voltage-sensing optical approaches. Logistical and ordinal linear regression models were constructed using drug responses as predictors and TdP risk categories as outcomes. Three of seven predictors (drug-induced arrhythmia-like events and prolongation of repolarization at either maximum tested or maximal clinical exposures) categorized drugs with reasonable accuracy (area under the curve values of receiver operator curves ~0.8). hiPSC-CM line, test site, and platform had minimal influence on drug categorization. These results demonstrate the utility of hiPSCCMs to detect drug-induced proarrhythmic effects as part of the evolving Comprehensive In Vitro Proarrhythmia Assay paradigm.
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spelling pubmed-62260302018-11-09 International Multisite Study of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Drug Proarrhythmic Potential Assessment Blinova, Ksenia Dang, Qianyu Millard, Daniel Smith, Godfrey Pierson, Jennifer Guo, Liang Brock, Mathew Lu, Hua Rong Kraushaar, Udo Zeng, Haoyu Shi, Hong Zhang, Xiaoyu Sawada, Kohei Osada, Tomoharu Kanda, Yasunari Sekino, Yuko Pang, Li Feaster, Tromondae K. Kettenhofen, Ralf Stockbridge, Norman Strauss, David G. Gintant, Gary Cell Rep Article To assess the utility of human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) as an in vitro proarrhythmia model, we evaluated the concentration dependence and sources of variability of electrophysiologic responses to 28 drugs linked to low, intermediate, and high torsades de pointes (TdP) risk categories using two commercial cell lines and standardized protocols in a blinded multisite study using multielectrode array or voltage-sensing optical approaches. Logistical and ordinal linear regression models were constructed using drug responses as predictors and TdP risk categories as outcomes. Three of seven predictors (drug-induced arrhythmia-like events and prolongation of repolarization at either maximum tested or maximal clinical exposures) categorized drugs with reasonable accuracy (area under the curve values of receiver operator curves ~0.8). hiPSC-CM line, test site, and platform had minimal influence on drug categorization. These results demonstrate the utility of hiPSCCMs to detect drug-induced proarrhythmic effects as part of the evolving Comprehensive In Vitro Proarrhythmia Assay paradigm. 2018-09-25 /pmc/articles/PMC6226030/ /pubmed/30257217 http://dx.doi.org/10.1016/j.celrep.2018.08.079 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Blinova, Ksenia
Dang, Qianyu
Millard, Daniel
Smith, Godfrey
Pierson, Jennifer
Guo, Liang
Brock, Mathew
Lu, Hua Rong
Kraushaar, Udo
Zeng, Haoyu
Shi, Hong
Zhang, Xiaoyu
Sawada, Kohei
Osada, Tomoharu
Kanda, Yasunari
Sekino, Yuko
Pang, Li
Feaster, Tromondae K.
Kettenhofen, Ralf
Stockbridge, Norman
Strauss, David G.
Gintant, Gary
International Multisite Study of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Drug Proarrhythmic Potential Assessment
title International Multisite Study of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Drug Proarrhythmic Potential Assessment
title_full International Multisite Study of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Drug Proarrhythmic Potential Assessment
title_fullStr International Multisite Study of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Drug Proarrhythmic Potential Assessment
title_full_unstemmed International Multisite Study of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Drug Proarrhythmic Potential Assessment
title_short International Multisite Study of Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes for Drug Proarrhythmic Potential Assessment
title_sort international multisite study of human-induced pluripotent stem cell-derived cardiomyocytes for drug proarrhythmic potential assessment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6226030/
https://www.ncbi.nlm.nih.gov/pubmed/30257217
http://dx.doi.org/10.1016/j.celrep.2018.08.079
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