Identifying drug interactions using machine learning


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Demirsoy I., KARAİBRAHİMOĞLU A.

Advances in Clinical and Experimental Medicine, cilt.32, sa.8, ss.829-838, 2023 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 32 Sayı: 8
  • Basım Tarihi: 2023
  • Doi Numarası: 10.17219/acem/169852
  • Dergi Adı: Advances in Clinical and Experimental Medicine
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, EMBASE, Directory of Open Access Journals
  • Sayfa Sayıları: ss.829-838
  • Anahtar Kelimeler: biostatistics, drug–drug interaction, machine learning algorithms, prediction, similarity matrices
  • Uşak Üniversitesi Adresli: Evet

Özet

Idris Demirsoy would like to thank all the people whose assistance was a milestone in the completion of this project. The author thanks Mondira Bhattacharya for introducing him to people who are expert in their field, Jaishri Meer for providing detailed information about drug–drug interactions and showing him MedDRA system, among others. The author would like to thank Tim Carlson for explaining the clinical drug–drug interactions, among others, Erhan Berber for emphasizing patient view on drug–drug interactions, Balachandra Ambiga for selecting him for the project, and Shereen McIntyre for believing in him and supporting him. The majority of Americans, accounting for 51% of the population, take 2 or more drugs daily. Unfortunately, nearly 100,000 people die annually as a result of adverse drug reactions (ADRs), making it the 4th most common cause of mortality in the USA. Drug–drug interactions (DDIs) and their impact on patients represent critical challenges for the healthcare system. To reduce the incidence of ADRs, this study focuses on identifying DDIs using a machine-learning approach. Drug-related information was obtained from various free databases, including DrugBank, BioGRID and Comparative Toxicogenomics Database. Eight similarity matrices between drugs were created as covariates in the model in order to assess their influence on DDIs. Three distinct machine learning algorithms were considered, namely, logistic regression (LR), eXtreme Gradient Boosting (XGBoost) and neural network (NN). Our study examined 22 notable drugs and their interactions with 841 other drugs from DrugBank. The accuracy of the machine learning approaches ranged from 68% to 78%, while the F1 scores ranged from 78% to 83%. Our study indicates that enzyme and target similarity are the most significant parameters in identifying DDIs. Finally, our data-driven approach reveals that machine learning methods can accurately predict DDIs and provide additional insights in a timely and cost-effective manner.