In Silico Safety Pharmacology on Intersubject Variability Population of Models: A Regression Model Approach

A. S. D. L. Nava, A. Liberos, I. Hernández-Romero, María de la Salud Guillem Sánchez, F. Atienza, F. Fernández‐Avilés, A. Climent
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Abstract

Safety pharmacology aims at detecting undesirable effect of drugs during its development. However, limitations are present at both in-vitro and in-silico level because of its low detection efficacy during this process. In this work, the effect of drugs at tissue level was studied and inducibility in a multivariable scenario including 127 models tested for two different tissue sizes (basal and dilated) and two conditions (no drug and isoproterenol) was obtained. From these models, maintenance duration (MD) of the reentry was calculated and a regression model based on Canonical Correlation Analysis (CCA) was implemented to evaluate the proarrhythmic effect of isoproterenol depending on model size. The number of models with AF maintenance was larger for dilated atria and isoproterenol. CCA analysis obtained 96% accuracy on an arrhythmogenicity test set for basal size and 100% on the dilated one. A new promising methodology was proposed for safety pharmacology including variability between patients, setting the base for personalized medicine.
计算机安全药理学的学科间变异模型群体:回归模型方法
安全药理学的目的是发现药物在开发过程中的不良作用。然而,由于其在此过程中的检测效率较低,因此在体外和芯片水平上都存在局限性。在这项工作中,研究了药物在组织水平上的作用,并在多变量情景下对127个模型进行了两种不同组织大小(基础和扩张)和两种条件(无药物和异丙肾上腺素)的诱导性测试。根据这些模型,计算再入维持时间(MD),并基于典型相关分析(CCA)建立回归模型,根据模型大小评估异丙肾上腺素的促心律失常作用。心房扩张组和异丙肾上腺素组维持房颤的模型数量较多。CCA分析在基础尺寸的致心律失常试验集上获得96%的准确性,在扩张尺寸上获得100%的准确性。提出了一种新的有前途的安全药理学方法,包括患者之间的差异,为个性化医疗奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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