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

机译:关于受试者间变异性模型的计算机安全药理学:回归模型方法

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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.
机译:安全药理学旨在检测药物在开发过程中的不良作用。然而,由于其在该过程中的低检测功效,因此在体外和计算机上均存在局限性。在这项工作中,研究了药物在组织水平上的作用,并在包括127种模型的多变量场景中对诱导性进行了测试,该模型针对两种不同的组织大小(基础组织和扩张组织)和两种条件(无药物和异丙肾上腺素)进行了测试。从这些模型中,计算出折返的维持时间(MD),并基于模型相关性使用基于典范相关分析(CCA)的回归模型来评估异丙肾上腺素的心律失常作用。对于扩张的心房和异丙肾上腺素,维持房颤的模型数量更多。在基本尺寸的心律失常性测试装置上,CCA分析获得了96%的准确度,在扩张的装置上获得了100%的准确度。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性,为个性化药物奠定了基础。

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