Similarity-based machine learning support vector machine predictor of drug-drug interactions with improved accuracies.
drug-drug interactions
machine learning
pairwise kernel
similarity-based model
support vector machines
Journal
Journal of clinical pharmacy and therapeutics
ISSN: 1365-2710
Titre abrégé: J Clin Pharm Ther
Pays: England
ID NLM: 8704308
Informations de publication
Date de publication:
Apr 2019
Apr 2019
Historique:
received:
29
05
2018
revised:
29
10
2018
accepted:
18
11
2018
pubmed:
20
12
2018
medline:
21
3
2019
entrez:
20
12
2018
Statut:
ppublish
Résumé
Drug-drug interactions (DDI) are frequent causes of adverse clinical drug reactions. Efforts have been directed at the early stage to achieve accurate identification of DDI for drug safety assessments, including the development of in silico predictive methods. In particular, similarity-based in silico methods have been developed to assess DDI with good accuracies, and machine learning methods have been employed to further extend the predictive range of similarity-based approaches. However, the performance of a developed machine learning method is lower than expectations partly because of the use of less diverse DDI training data sets and a less optimal set of similarity measures. In this work, we developed a machine learning model using support vector machines (SVMs) based on the literature-reported established set of similarity measures and comprehensive training data sets. The established similarity measures include the 2D molecular structure similarity, 3D pharmacophoric similarity, interaction profile fingerprint (IPF) similarity, target similarity and adverse drug effect (ADE) similarity, which were extracted from well-known databases, such as DrugBank and Side Effect Resource (SIDER). A pairwise kernel was constructed for the known and possible drug pairs based on the five established similarity measures and then used as the input vector of the SVM. The 10-fold cross-validation studies showed a predictive performance of AUROC >0.97, which is significantly improved compared with the AUROC of 0.67 of an analogously developed machine learning model. Our study suggested that a similarity-based SVM prediction is highly useful for identifying DDI. in silico methods based on multifarious drug similarities have been suggested to be feasible for DDI prediction in various studies. In this way, our pairwise kernel SVM model had better accuracies than some previous works, which can be used as a pharmacovigilance tool to detect potential DDI.
Types de publication
Journal Article
Validation Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
268-275Subventions
Organisme : Guizhou Provincial Administration of Traditional Chinese Medicine for Traditional Chinese Medicine program
ID : QZYY-2018-063
Organisme : the National Natural Science Foundation of China
ID : 81373482
Organisme : the National Natural Science Foundation of China
ID : 81373378
Organisme : The Fundamental Research Funds for the Central Universities
ID : ZJ14040
Organisme : The High Performance Computing Center at China Pharmaceutical University
Organisme : Key clinical specialty construction project in Guizhou province in 2016
Organisme : Construction project of surgical talent base in Guizhou province in 2014
Informations de copyright
© 2018 John Wiley & Sons Ltd.