Cargando…
Integrating Multiple Evidence Sources to Predict Adverse Drug Reactions Based on a Systems Pharmacology Model
Identifying potential adverse drug reactions (ADRs) is critically important for drug discovery and public health. Here we developed a multiple evidence fusion (MEF) method for the large-scale prediction of drug ADRs that can handle both approved drugs and novel molecules. MEF is based on the similar...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592529/ https://www.ncbi.nlm.nih.gov/pubmed/26451329 http://dx.doi.org/10.1002/psp4.12002 |
_version_ | 1782393201210949632 |
---|---|
author | Cao, D-S Xiao, N Li, Y-J Zeng, W-B Liang, Y-Z Lu, A-P Xu, Q-S Chen, AF |
author_facet | Cao, D-S Xiao, N Li, Y-J Zeng, W-B Liang, Y-Z Lu, A-P Xu, Q-S Chen, AF |
author_sort | Cao, D-S |
collection | PubMed |
description | Identifying potential adverse drug reactions (ADRs) is critically important for drug discovery and public health. Here we developed a multiple evidence fusion (MEF) method for the large-scale prediction of drug ADRs that can handle both approved drugs and novel molecules. MEF is based on the similarity reference by collaborative filtering, and integrates multiple similarity measures from various data types, taking advantage of the complementarity in the data. We used MEF to integrate drug-related and ADR-related data from multiple levels, including the network structural data formed by known drug–ADR relationships for predicting likely unknown ADRs. On cross-validation, it obtains high sensitivity and specificity, substantially outperforming existing methods that utilize single or a few data types. We validated our prediction by their overlap with drug–ADR associations that are known in databases. The proposed computational method could be used for complementary hypothesis generation and rapid analysis of potential drug–ADR interactions. |
format | Online Article Text |
id | pubmed-4592529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45925292015-10-08 Integrating Multiple Evidence Sources to Predict Adverse Drug Reactions Based on a Systems Pharmacology Model Cao, D-S Xiao, N Li, Y-J Zeng, W-B Liang, Y-Z Lu, A-P Xu, Q-S Chen, AF CPT Pharmacometrics Syst Pharmacol Original Articles Identifying potential adverse drug reactions (ADRs) is critically important for drug discovery and public health. Here we developed a multiple evidence fusion (MEF) method for the large-scale prediction of drug ADRs that can handle both approved drugs and novel molecules. MEF is based on the similarity reference by collaborative filtering, and integrates multiple similarity measures from various data types, taking advantage of the complementarity in the data. We used MEF to integrate drug-related and ADR-related data from multiple levels, including the network structural data formed by known drug–ADR relationships for predicting likely unknown ADRs. On cross-validation, it obtains high sensitivity and specificity, substantially outperforming existing methods that utilize single or a few data types. We validated our prediction by their overlap with drug–ADR associations that are known in databases. The proposed computational method could be used for complementary hypothesis generation and rapid analysis of potential drug–ADR interactions. John Wiley & Sons, Ltd 2015-09 2015-09-11 /pmc/articles/PMC4592529/ /pubmed/26451329 http://dx.doi.org/10.1002/psp4.12002 Text en © 2015 The Authors CPT: Pharmacometrics & Systems Pharmacology published by Wiley Periodicals, Inc. on behalf of American Society for Clinical Pharmacology and Therapeutics. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Cao, D-S Xiao, N Li, Y-J Zeng, W-B Liang, Y-Z Lu, A-P Xu, Q-S Chen, AF Integrating Multiple Evidence Sources to Predict Adverse Drug Reactions Based on a Systems Pharmacology Model |
title | Integrating Multiple Evidence Sources to Predict Adverse Drug Reactions Based on a Systems Pharmacology Model |
title_full | Integrating Multiple Evidence Sources to Predict Adverse Drug Reactions Based on a Systems Pharmacology Model |
title_fullStr | Integrating Multiple Evidence Sources to Predict Adverse Drug Reactions Based on a Systems Pharmacology Model |
title_full_unstemmed | Integrating Multiple Evidence Sources to Predict Adverse Drug Reactions Based on a Systems Pharmacology Model |
title_short | Integrating Multiple Evidence Sources to Predict Adverse Drug Reactions Based on a Systems Pharmacology Model |
title_sort | integrating multiple evidence sources to predict adverse drug reactions based on a systems pharmacology model |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592529/ https://www.ncbi.nlm.nih.gov/pubmed/26451329 http://dx.doi.org/10.1002/psp4.12002 |
work_keys_str_mv | AT caods integratingmultipleevidencesourcestopredictadversedrugreactionsbasedonasystemspharmacologymodel AT xiaon integratingmultipleevidencesourcestopredictadversedrugreactionsbasedonasystemspharmacologymodel AT liyj integratingmultipleevidencesourcestopredictadversedrugreactionsbasedonasystemspharmacologymodel AT zengwb integratingmultipleevidencesourcestopredictadversedrugreactionsbasedonasystemspharmacologymodel AT liangyz integratingmultipleevidencesourcestopredictadversedrugreactionsbasedonasystemspharmacologymodel AT luap integratingmultipleevidencesourcestopredictadversedrugreactionsbasedonasystemspharmacologymodel AT xuqs integratingmultipleevidencesourcestopredictadversedrugreactionsbasedonasystemspharmacologymodel AT chenaf integratingmultipleevidencesourcestopredictadversedrugreactionsbasedonasystemspharmacologymodel |