Application of Convolutional Neural Networks Using Action Potential Shape for In-Silico Proarrhythmic Risk Assessment

被引:3
|
作者
Jeong, Da Un [1 ]
Yoo, Yedam [1 ]
Marcellinus, Aroli [1 ]
Lim, Ki Moo [1 ,2 ,3 ]
机构
[1] Kumoh Natl Inst Technol, Dept IT Convergence Engn, Gumi 39253, South Korea
[2] Kumoh Natl Inst Technol, Dept Med IT Convergence Engn, Gumi 39253, South Korea
[3] Meta Heart Inc, Gumi 39253, South Korea
基金
新加坡国家研究基金会;
关键词
drug screening; action potential shape; convolutional neural network; TORSADE-DE-POINTES; INTERVAL PROLONGATION; PREDICTION; DRUGS;
D O I
10.3390/biomedicines11020406
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study proposes a convolutional neural network (CNN) model using action potential (AP) shapes as input for proarrhythmic risk assessment, considering the hypothesis that machine-learning features automatically extracted from AP shapes contain more meaningful information than do manually extracted indicators. We used 28 drugs listed in the comprehensive in vitro proarrhythmia assay (CiPA), consisting of eight high-risk, eleven intermediate-risk, and nine low-risk torsadogenic drugs. We performed drug simulations to generate AP shapes using experimental drug data, obtaining 2000 AP shapes per drug. The proposed CNN model was trained to classify the TdP risk into three levels, high-, intermediate-, and low-risk, based on in silico AP shapes generated using 12 drugs. We then evaluated the performance of the proposed model for 16 drugs. The classification accuracy of the proposed CNN model was excellent for high- and low-risk drugs, with AUCs of 0.914 and 0.951, respectively. The model performance for intermediate-risk drugs was good, at 0.814. Our proposed model can accurately assess the TdP risks of drugs from in silico AP shapes, reflecting the pharmacokinetics of ionic currents. We need to secure more drugs for future studies to improve the TdP-risk-assessment robustness.
引用
收藏
页数:13
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