基于BioBERT和BLSTM的生物医学文本药物-药物相互作用提取

IF 4 Q2 COMPUTER SCIENCE, ARTIFICIAL INTELLIGENCE
Maryam KafiKang, Abdeltawab Hendawi
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引用次数: 1

摘要

在药物领域,当两种或多种药物相互作用时,就会发生药物-药物相互作用(ddi),可能会改变药物的预期效果,并导致不良的患者健康结果。因此,识别和理解这些相互作用是至关重要的。近年来,越来越多的新化合物被发现,从而发现了许多新的ddi。需要有效的方法来提取和分析ddi,因为大多数此类信息仍然主要位于生物医学文章和来源中。尽管发展了各种技术,但准确预测ddi仍然是一个重大挑战。本文提出了一种新的解决方案,利用关系生物记忆(R-BioBERT)对ddi进行检测和分类,并利用双向长短期记忆(BLSTM)来提高预测的准确性。除了确定两种药物是否相互作用外,该方法还确定了它们之间相互作用的具体类型。结果表明,与我们的基线模型相比,使用BLSTM可以显著提高f分数,这在三个著名的DDI提取数据集(包括SemEval 2013、TAC 2018和TAC 2019)上得到了证明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug-Drug Interaction Extraction from Biomedical Text Using Relation BioBERT with BLSTM
In the context of pharmaceuticals, drug-drug interactions (DDIs) occur when two or more drugs interact, potentially altering the intended effects of the drugs and resulting in adverse patient health outcomes. Therefore, it is essential to identify and comprehend these interactions. In recent years, an increasing number of novel compounds have been discovered, resulting in the discovery of numerous new DDIs. There is a need for effective methods to extract and analyze DDIs, as the majority of this information is still predominantly located in biomedical articles and sources. Despite the development of various techniques, accurately predicting DDIs remains a significant challenge. This paper proposes a novel solution to this problem by leveraging the power of Relation BioBERT (R-BioBERT) to detect and classify DDIs and the Bidirectional Long Short-Term Memory (BLSTM) to improve the accuracy of predictions. In addition to determining whether two drugs interact, the proposed method also identifies the specific types of interactions between them. Results show that the use of BLSTM leads to significantly higher F-scores compared to our baseline model, as demonstrated on three well-known DDI extraction datasets that includes SemEval 2013, TAC 2018, and TAC 2019.
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来源期刊
CiteScore
6.30
自引率
0.00%
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审稿时长
7 weeks
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