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Identifying the serious clinical outcomes of adverse reactions to drugs by a multi-task deep learning framework
Adverse Drug Reactions (ADRs) have a direct impact on human health. As continuous pharmacovigilance and drug monitoring prove to be costly and time-consuming, computational methods have emerged as promising alternatives. However, most existing computational methods primarily focus on predicting whet...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449791/ https://www.ncbi.nlm.nih.gov/pubmed/37620651 http://dx.doi.org/10.1038/s42003-023-05243-w |
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author | Zhao, Haochen Ni, Peng Zhao, Qichang Liang, Xiao Ai, Di Erhardt, Shannon Wang, Jun Li, Yaohang Wang, Jianxin |
author_facet | Zhao, Haochen Ni, Peng Zhao, Qichang Liang, Xiao Ai, Di Erhardt, Shannon Wang, Jun Li, Yaohang Wang, Jianxin |
author_sort | Zhao, Haochen |
collection | PubMed |
description | Adverse Drug Reactions (ADRs) have a direct impact on human health. As continuous pharmacovigilance and drug monitoring prove to be costly and time-consuming, computational methods have emerged as promising alternatives. However, most existing computational methods primarily focus on predicting whether or not the drug is associated with an adverse reaction and do not consider the core issue of drug benefit-risk assessment—whether the treatment outcome is serious when adverse drug reactions occur. To this end, we categorize serious clinical outcomes caused by adverse reactions to drugs into seven distinct classes and present a deep learning framework, so-called GCAP, for predicting the seriousness of clinical outcomes of adverse reactions to drugs. GCAP has two tasks: one is to predict whether adverse reactions to drugs cause serious clinical outcomes, and the other is to infer the corresponding classes of serious clinical outcomes. Experimental results demonstrate that our method is a powerful and robust framework with high extendibility. GCAP can serve as a useful tool to successfully address the challenge of predicting the seriousness of clinical outcomes stemming from adverse reactions to drugs. |
format | Online Article Text |
id | pubmed-10449791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104497912023-08-26 Identifying the serious clinical outcomes of adverse reactions to drugs by a multi-task deep learning framework Zhao, Haochen Ni, Peng Zhao, Qichang Liang, Xiao Ai, Di Erhardt, Shannon Wang, Jun Li, Yaohang Wang, Jianxin Commun Biol Article Adverse Drug Reactions (ADRs) have a direct impact on human health. As continuous pharmacovigilance and drug monitoring prove to be costly and time-consuming, computational methods have emerged as promising alternatives. However, most existing computational methods primarily focus on predicting whether or not the drug is associated with an adverse reaction and do not consider the core issue of drug benefit-risk assessment—whether the treatment outcome is serious when adverse drug reactions occur. To this end, we categorize serious clinical outcomes caused by adverse reactions to drugs into seven distinct classes and present a deep learning framework, so-called GCAP, for predicting the seriousness of clinical outcomes of adverse reactions to drugs. GCAP has two tasks: one is to predict whether adverse reactions to drugs cause serious clinical outcomes, and the other is to infer the corresponding classes of serious clinical outcomes. Experimental results demonstrate that our method is a powerful and robust framework with high extendibility. GCAP can serve as a useful tool to successfully address the challenge of predicting the seriousness of clinical outcomes stemming from adverse reactions to drugs. Nature Publishing Group UK 2023-08-24 /pmc/articles/PMC10449791/ /pubmed/37620651 http://dx.doi.org/10.1038/s42003-023-05243-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Zhao, Haochen Ni, Peng Zhao, Qichang Liang, Xiao Ai, Di Erhardt, Shannon Wang, Jun Li, Yaohang Wang, Jianxin Identifying the serious clinical outcomes of adverse reactions to drugs by a multi-task deep learning framework |
title | Identifying the serious clinical outcomes of adverse reactions to drugs by a multi-task deep learning framework |
title_full | Identifying the serious clinical outcomes of adverse reactions to drugs by a multi-task deep learning framework |
title_fullStr | Identifying the serious clinical outcomes of adverse reactions to drugs by a multi-task deep learning framework |
title_full_unstemmed | Identifying the serious clinical outcomes of adverse reactions to drugs by a multi-task deep learning framework |
title_short | Identifying the serious clinical outcomes of adverse reactions to drugs by a multi-task deep learning framework |
title_sort | identifying the serious clinical outcomes of adverse reactions to drugs by a multi-task deep learning framework |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10449791/ https://www.ncbi.nlm.nih.gov/pubmed/37620651 http://dx.doi.org/10.1038/s42003-023-05243-w |
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