Use of Biomedical Ontologies for Integration of Biological Knowledge for Learning and Prediction of Adverse Drug Reactions.

Gene regulation and systems biology Pub Date : 2017-03-15 eCollection Date: 2017-01-01 DOI:10.1177/1177625017696075
Shadia Zaman, Sirarat Sarntivijai, Darrell R Abernethy
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引用次数: 14

Abstract

Drug-induced toxicity is a major public health concern that leads to patient morbidity and mortality. To address this problem, the Food and Drug Administration is working on the PredicTox initiative, a pilot research program on tyrosine kinase inhibitors, to build mechanistic and predictive models for drug-induced toxicity. This program involves integrating data acquired during preclinical studies and clinical trials within pharmaceutical company development programs that they have agreed to put in the public domain and in publicly available biological, pharmacological, and chemical databases. The integration process is accommodated by biomedical ontologies, a set of standardized vocabularies that define terms and logical relationships between them in each vocabulary. We describe a few programs that have used ontologies to address biomedical questions. The PredicTox effort is leveraging the experience gathered from these early initiatives to develop an infrastructure that allows evaluation of the hypothesis that having a mechanistic understanding underlying adverse drug reactions will improve the capacity to understand drug-induced clinical adverse drug reactions.

Abstract Image

Abstract Image

利用生物医学本体整合生物知识,以学习和预测药物不良反应。
药物毒性是导致患者发病和死亡的主要公共卫生问题。为了解决这个问题,美国食品和药物管理局正在开展PredicTox计划,这是一个关于酪氨酸激酶抑制剂的试点研究项目,旨在建立药物毒性的机制和预测模型。该项目涉及整合制药公司开发项目中临床前研究和临床试验期间获得的数据,这些数据已同意放入公共领域,并公开提供生物、药理学和化学数据库。生物医学本体是一组标准化词汇表,用于定义术语和每个词汇表中术语之间的逻辑关系。我们描述了一些使用本体来解决生物医学问题的程序。PredicTox项目正在利用从这些早期倡议中收集的经验来开发一个基础设施,该基础设施允许对假设进行评估,即对药物不良反应的机制了解将提高了解药物引起的临床药物不良反应的能力。
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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