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TMFUF: a triple matrix factorization-based unified framework for predicting comprehensive drug-drug interactions of new drugs

BACKGROUND: A significant number of adverse drug reactions is caused by unexpected Drug-drug interactions (DDIs). The identification of DDIs becomes crucial before the co-prescription of multiple drugs is made. Such a task in clinics or in drug discovery usually requires high costs and numerous limi...

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Autores principales: Shi, Jian-Yu, Huang, Hua, Li, Jia-Xin, Lei, Peng, Zhang, Yan-Ning, Dong, Kai, Yiu, Siu-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245591/
https://www.ncbi.nlm.nih.gov/pubmed/30453924
http://dx.doi.org/10.1186/s12859-018-2379-8
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author Shi, Jian-Yu
Huang, Hua
Li, Jia-Xin
Lei, Peng
Zhang, Yan-Ning
Dong, Kai
Yiu, Siu-Ming
author_facet Shi, Jian-Yu
Huang, Hua
Li, Jia-Xin
Lei, Peng
Zhang, Yan-Ning
Dong, Kai
Yiu, Siu-Ming
author_sort Shi, Jian-Yu
collection PubMed
description BACKGROUND: A significant number of adverse drug reactions is caused by unexpected Drug-drug interactions (DDIs). The identification of DDIs becomes crucial before the co-prescription of multiple drugs is made. Such a task in clinics or in drug discovery usually requires high costs and numerous limitations, while computational approaches are able to predict potential DDIs effectively by utilizing diverse drug attributes (e.g. side effects). Nevertheless, they’re incapable when required to predict enhancive and degressive DDIs, which change increasingly and decreasingly the pharmacological behavior of interacting drugs respectively. The pharmacological change of DDIs is one of the most important factors when making a multi-drug prescription. RESULTS: In this work, we design a Triple Matrix Factorization-based Unified Framework (TMFUF) to address the above issue. By leveraging a group of side effect entries of drugs, TMFUF achieves the inspiring result (AUC = 0.842 and AUPR = 0.526) in the case of conventional DDI prediction under the traditional screening task. In the comparison with two state-of-the-art approaches, TMFUF demonstrates it superiority by ~ 7% and ~ 20% improvement in terms of AUC and AUPR respectively. More importantly, TMFUF shows its ability in the comprehensive DDI prediction under different screening tasks. Finally, a utilization TMFUF reveals the significant pairs of side effects, which contribute to form enhancive and degressive DDIs, for further clinical validation. CONCLUSIONS: The proposed TMFUF is first capable to predict both conventional binary DDIs and comprehensive DDIs such that it captures the pharmacological changes caused by DDIs. Furthermore, it provides a unified solution of DDI prediction for two screening scenarios, which involves newly given drugs having no prior interaction. Another advantage is its ability to indicate how significantly the pairs of drug features contribute to form DDIs.
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spelling pubmed-62455912018-11-26 TMFUF: a triple matrix factorization-based unified framework for predicting comprehensive drug-drug interactions of new drugs Shi, Jian-Yu Huang, Hua Li, Jia-Xin Lei, Peng Zhang, Yan-Ning Dong, Kai Yiu, Siu-Ming BMC Bioinformatics Research BACKGROUND: A significant number of adverse drug reactions is caused by unexpected Drug-drug interactions (DDIs). The identification of DDIs becomes crucial before the co-prescription of multiple drugs is made. Such a task in clinics or in drug discovery usually requires high costs and numerous limitations, while computational approaches are able to predict potential DDIs effectively by utilizing diverse drug attributes (e.g. side effects). Nevertheless, they’re incapable when required to predict enhancive and degressive DDIs, which change increasingly and decreasingly the pharmacological behavior of interacting drugs respectively. The pharmacological change of DDIs is one of the most important factors when making a multi-drug prescription. RESULTS: In this work, we design a Triple Matrix Factorization-based Unified Framework (TMFUF) to address the above issue. By leveraging a group of side effect entries of drugs, TMFUF achieves the inspiring result (AUC = 0.842 and AUPR = 0.526) in the case of conventional DDI prediction under the traditional screening task. In the comparison with two state-of-the-art approaches, TMFUF demonstrates it superiority by ~ 7% and ~ 20% improvement in terms of AUC and AUPR respectively. More importantly, TMFUF shows its ability in the comprehensive DDI prediction under different screening tasks. Finally, a utilization TMFUF reveals the significant pairs of side effects, which contribute to form enhancive and degressive DDIs, for further clinical validation. CONCLUSIONS: The proposed TMFUF is first capable to predict both conventional binary DDIs and comprehensive DDIs such that it captures the pharmacological changes caused by DDIs. Furthermore, it provides a unified solution of DDI prediction for two screening scenarios, which involves newly given drugs having no prior interaction. Another advantage is its ability to indicate how significantly the pairs of drug features contribute to form DDIs. BioMed Central 2018-11-20 /pmc/articles/PMC6245591/ /pubmed/30453924 http://dx.doi.org/10.1186/s12859-018-2379-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Shi, Jian-Yu
Huang, Hua
Li, Jia-Xin
Lei, Peng
Zhang, Yan-Ning
Dong, Kai
Yiu, Siu-Ming
TMFUF: a triple matrix factorization-based unified framework for predicting comprehensive drug-drug interactions of new drugs
title TMFUF: a triple matrix factorization-based unified framework for predicting comprehensive drug-drug interactions of new drugs
title_full TMFUF: a triple matrix factorization-based unified framework for predicting comprehensive drug-drug interactions of new drugs
title_fullStr TMFUF: a triple matrix factorization-based unified framework for predicting comprehensive drug-drug interactions of new drugs
title_full_unstemmed TMFUF: a triple matrix factorization-based unified framework for predicting comprehensive drug-drug interactions of new drugs
title_short TMFUF: a triple matrix factorization-based unified framework for predicting comprehensive drug-drug interactions of new drugs
title_sort tmfuf: a triple matrix factorization-based unified framework for predicting comprehensive drug-drug interactions of new drugs
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245591/
https://www.ncbi.nlm.nih.gov/pubmed/30453924
http://dx.doi.org/10.1186/s12859-018-2379-8
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