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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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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. |
format | Online Article Text |
id | pubmed-6226030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
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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