Drug-Drug Interaction Extraction from Biomedical Texts via Relation BERT

Dinh Phuong Nguyen, T. Ho
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引用次数: 7

Abstract

There is a large number of drugs introduced every year and a number of interactions between drugs also has quick growth. As a result, biomedical texts following new drugs and interactions expand [15]. Several published studies of drug safety have revealed that drug-drug interactions (DDIs) may be detected too late, when millions of patients have already been exposed [25]. Therefore, the management of drug drug interactions is critical issue since the importance of known drug drug interaction and the giant amount of available information around them [5]. Thus, the issue creates an imperative need for the development of high-reliable automatic DDI extraction methods while manual DDI extraction is time-consuming and could lead to out-of-date information. However, the accuracy of the current automatic DDI extraction method is still insufficient for the practical application. In this research, we explore the Relation Bidirectional Encoder Representations from Transformers (Relation BERT) architecture [32] to detect and classify DDIs from biomedical texts using the DDI extraction 2013 corpus [5] and present three proposed models namely R-BERT∗, R-BioBERT1, and R-BioBERT2. From our knowledge, we are the first to investigate the potential of Relation BERT for the aim of accuracy improvement in DDI extraction. By using the state-of-the-art word representation method, three models produce macro-average F1-score of over 79%. Moreover, the accuracy of extracting Advice and Mechanism interaction achieves 90.63% and 97% respectively in terms of F1-score. The high accuracy of the model in Advice and Mechanism interaction creates motivation for wide application of automatic DDI extraction to the practice with high-reliable and humanless.
基于关系BERT的生物医学文本药物-药物相互作用提取
每年都有大量的药物被引入,药物之间的相互作用也在快速增长。因此,新的药物和相互作用之后的生物医学文本扩展了[15]。几项已发表的药物安全性研究表明,当数百万患者已经暴露于药物中时,药物-药物相互作用(ddi)可能被发现得太晚[25]。因此,鉴于已知药物相互作用的重要性以及围绕药物相互作用的大量可用信息,药物相互作用的管理是一个关键问题[5]。因此,该问题迫切需要开发高可靠的自动DDI提取方法,而手动DDI提取既耗时又可能导致信息过时。然而,目前的自动DDI提取方法的精度对于实际应用来说仍然不足。在本研究中,我们利用2013年DDI提取语料库[5],探索了来自变形器的关系双向编码器表示(Relation BERT)架构[32]来检测和分类生物医学文本中的DDI,并提出了三个模型,即R-BERT∗,R-BioBERT1和R-BioBERT2。据我们所知,我们是第一个研究关系BERT的潜力,以提高DDI提取的准确性。通过使用最先进的单词表示方法,三个模型的宏观平均f1得分超过79%。在F1-score上,Advice和Mechanism interaction的提取准确率分别达到90.63%和97%。该模型在建议和机制交互方面的高准确性为DDI自动提取在高可靠、无人工的实践中广泛应用提供了动力。
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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