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Stan: A Probabilistic Programming Language.斯坦:一种概率编程语言。
J Stat Softw. 2017;76. doi: 10.18637/jss.v076.i01. Epub 2017 Jan 11.
2
A human population-based organotypic in vitro model for cardiotoxicity screening.用于心脏毒性筛选的基于人体的器官型体外模型。
ALTEX. 2018;35(4):441-452. doi: 10.14573/altex.1805301. Epub 2018 Jul 8.
3
CiPA challenges and opportunities from a non-clinical, clinical and regulatory perspectives. An overview of the safety pharmacology scientific discussion.从非临床、临床和监管角度看CiPA面临的挑战与机遇。安全药理学科学讨论概述。
J Pharmacol Toxicol Methods. 2018 Sep-Oct;93:15-25. doi: 10.1016/j.vascn.2018.06.005. Epub 2018 Jun 27.
4
Effects of moxifloxacin on the proarrhythmic surrogate markers in healthy Filipino subjects: Exposure-response modeling using ECG data of thorough QT/QTc study.莫西沙星对健康菲律宾受试者致心律失常替代标志物的影响:基于全面 QT/QTc 研究 ECG 数据的暴露-反应关系建模。
J Pharmacol Sci. 2018 Apr;136(4):234-241. doi: 10.1016/j.jphs.2018.01.009. Epub 2018 Mar 27.
5
Assessing QT/QTc interval prolongation with concentration-QT modeling for Phase I studies: impact of computational platforms, model structures and confidence interval calculation methods.评估 I 期研究中浓度- QT 模型的 QT/QTc 间期延长:计算平台、模型结构和置信区间计算方法的影响。
J Pharmacokinet Pharmacodyn. 2018 Jun;45(3):469-482. doi: 10.1007/s10928-018-9582-0. Epub 2018 Mar 19.
6
Study Design Parameters Affecting Exposure Response Analysis of QT Data: Results From Simulation Studies.影响QT数据暴露反应分析的研究设计参数:模拟研究结果
J Clin Pharmacol. 2018 May;58(5):674-685. doi: 10.1002/jcph.1065. Epub 2018 Feb 8.
7
Scientific white paper on concentration-QTc modeling.浓度-QTc 建模的科学白皮书。
J Pharmacokinet Pharmacodyn. 2018 Jun;45(3):383-397. doi: 10.1007/s10928-017-9558-5. Epub 2017 Dec 5.
8
Human Induced Pluripotent Stem Cell (hiPSC)-Derived Cells to Assess Drug Cardiotoxicity: Opportunities and Problems.人诱导多能干细胞(hiPSC)衍生细胞评估药物心脏毒性:机遇与问题。
Annu Rev Pharmacol Toxicol. 2018 Jan 6;58:83-103. doi: 10.1146/annurev-pharmtox-010617-053110. Epub 2017 Oct 6.
9
Mechanistic Model-Informed Proarrhythmic Risk Assessment of Drugs: Review of the "CiPA" Initiative and Design of a Prospective Clinical Validation Study.基于机制模型的药物致心律失常风险评估:“CiPA”计划综述及前瞻性临床验证研究设计
Clin Pharmacol Ther. 2018 Jan;103(1):54-66. doi: 10.1002/cpt.896. Epub 2017 Nov 16.
10
An Analysis of the Relationship Between Preclinical and Clinical QT Interval-Related Data.临床前与临床 QT 间期相关数据关系分析。
Toxicol Sci. 2017 Sep 1;159(1):94-101. doi: 10.1093/toxsci/kfx125.

在体 QT/QTc 研究:准确预测临床浓度-QTc 关系的体外人类模型。

Thorough QT/QTc in a Dish: An In Vitro Human Model That Accurately Predicts Clinical Concentration-QTc Relationships.

机构信息

Department of Veterinary Integrative Biosciences, Texas A&M University, College Station, Texas, USA.

出版信息

Clin Pharmacol Ther. 2019 May;105(5):1175-1186. doi: 10.1002/cpt.1259. Epub 2018 Dec 2.

DOI:10.1002/cpt.1259
PMID:30346629
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6465173/
Abstract

"Thorough QT/corrected QT (QTc)" (TQT) studies are cornerstones of clinical cardiovascular safety assessment. However, TQT studies are resource intensive, and preclinical models predictive of the threshold of regulatory concern are lacking. We hypothesized that an in vitro model using induced pluripotent stem cell (iPSC)-derived cardiomyocytes from a diverse sample of human subjects can serve as a "TQT study in a dish." For 10 positive and 3 negative control drugs, in vitro concentration-QTc, computed using a population Bayesian model, accurately predicted known in vivo concentration-QTc. Moreover, predictions of the percent confidence that the regulatory threshold of 10 ms QTc prolongation would be breached were also consistent with in vivo evidence. This "TQT study in a dish," consisting of a population-based iPSC-derived cardiomyocyte model and Bayesian concentration-QTc modeling, has several advantages over existing in vitro platforms, including higher throughput, lower cost, and the ability to accurately predict the in vivo concentration range below the threshold of regulatory concern.

摘要

“全面 QT/校正 QT(QTc)”(TQT)研究是临床心血管安全性评估的基石。然而,TQT 研究需要大量资源,并且缺乏能够预测监管关注阈值的临床前模型。我们假设,使用来自不同人类受试者的诱导多能干细胞(iPSC)衍生的心肌细胞的体外模型可以作为“TQT 研究在培养皿中”。对于 10 种阳性和 3 种阴性对照药物,使用群体贝叶斯模型计算的体外浓度-QTc 准确预测了已知的体内浓度-QTc。此外,预测监管阈值 10ms QTc 延长的置信度百分比与体内证据也一致。这种“TQT 研究在培养皿中”,由基于群体的 iPSC 衍生的心肌细胞模型和贝叶斯浓度-QTc 建模组成,与现有的体外平台相比具有几个优势,包括更高的通量、更低的成本,并且能够准确预测监管关注阈值以下的体内浓度范围。