Contrastive learning of adverse events to provide effective and interpretable vector representations for machine-assisted pharmacovigilance.

IF 7.3 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Olivér M Balogh, Mátyás Pétervári, Áron M Csernák, Eszter Puhl, András Horváth, Péter Ferdinandy, Bence Ágg
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引用次数: 0

Abstract

Post-marketing surveillance is crucial for drug safety, yet the tools of pharmacovigilance rely solely on text-based data that may limit contemporary machine learning methodologies in the support of decision-making. With the recent surge of employing large language models (LLMs) for text-based tasks, there also arises an unmet need for a different approach which is not grounded in the linguistic patterns of unfiltered natural text, like LLMs, but rather based on real-world drug safety data. Here, we adapt contrastive learning algorithms to generate adverse event vector representations from spontaneous adverse event reports to serve as machine-readable (i.e. numerical) resources for downstream pharmacovigilance applications, such as drug-event association prediction for signal detection or causality assessment. We present comprehensive interpretability analyses of the resulting representations through density-based clustering, semantic evaluation, and comparison of multivariate dispersions, revealing patterns that reflect both functional and causal relations of the adverse events while also capturing drug-safety-related information better than existing medical terminologies and encoder-only LLMs. Furthermore, we demonstrate the applicability of our representations as input features in our downstream classifier model, outperforming the reporting odds ratio method, commonly used by regulatory agencies, and also LLM-generated representations (area under the receiver operating characteristic curve: 0.88 versus 0.76-0.83) on drug-event association prediction benchmarks. Therefore, we propose an interpretable adverse event vector representation, serving as a general resource that could enable the development of a wide array of machine learning applications to support decision-making in pharmacovigilance and facilitate patient safety.

不良事件的对比学习,为机器辅助药物警戒提供有效和可解释的载体表示。
上市后监测对药物安全至关重要,然而药物警戒工具仅依赖于基于文本的数据,这可能会限制当代机器学习方法在支持决策方面的作用。随着最近在基于文本的任务中使用大型语言模型(llm)的激增,也出现了对一种不同方法的需求,这种方法不像llm那样基于未经过滤的自然文本的语言模式,而是基于现实世界的药物安全数据。在这里,我们采用对比学习算法从自发不良事件报告中生成不良事件向量表示,作为下游药物警戒应用的机器可读(即数字)资源,例如用于信号检测或因果关系评估的药物事件关联预测。我们通过基于密度的聚类、语义评估和多变量离散度的比较,对结果表示进行了全面的可解释性分析,揭示了反映不良事件的功能和因果关系的模式,同时也比现有的医学术语和仅编码的llm更好地捕获了药物安全相关信息。此外,我们证明了我们的表征作为下游分类器模型输入特征的适用性,在药物事件关联预测基准上优于监管机构常用的报告比值比方法,以及llm生成的表征(接收者工作特征曲线下面积:0.88 vs 0.76-0.83)。因此,我们提出了一种可解释的不良事件向量表示,作为一种通用资源,可以开发广泛的机器学习应用程序,以支持药物警戒中的决策并促进患者安全。
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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来源期刊
Briefings in bioinformatics
Briefings in bioinformatics 生物-生化研究方法
CiteScore
13.20
自引率
13.70%
发文量
549
审稿时长
6 months
期刊介绍: Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data. The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.
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