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A weighted non-negative matrix factorization approach to predict potential associations between drug and disease.
Wang, Mei-Neng; Xie, Xue-Jun; You, Zhu-Hong; Ding, De-Wu; Wong, Leon.
Afiliação
  • Wang MN; School of Mathematics and Computer Science, Yichun University, Yichun, 336000, Jiangxi, China.
  • Xie XJ; School of Mathematics and Computer Science, Yichun University, Yichun, 336000, Jiangxi, China.
  • You ZH; School of Computer Science, Northwestern Polytechnical University, Xi'an, 710072, China. zhuhongyou@nwpu.edu.cn.
  • Ding DW; School of Mathematics and Computer Science, Yichun University, Yichun, 336000, Jiangxi, China. dwding2008@aliyun.com.
  • Wong L; Xinjiang Technical Institutes of Physics and Chemistry, Chinese Academy of Sciences, Urumqi, 830011, China.
J Transl Med ; 20(1): 552, 2022 12 03.
Article em En | MEDLINE | ID: mdl-36463215
ABSTRACT

BACKGROUND:

Associations of drugs with diseases provide important information for expediting drug development. Due to the number of known drug-disease associations is still insufficient, and considering that inferring associations between them through traditional in vitro experiments is time-consuming and costly. Therefore, more accurate and reliable computational methods urgent need to be developed to predict potential associations of drugs with diseases.

METHODS:

In this study, we present the model called weighted graph regularized collaborative non-negative matrix factorization for drug-disease association prediction (WNMFDDA). More specifically, we first calculated the drug similarity and disease similarity based on the chemical structures of drugs and medical description information of diseases, respectively. Then, to extend the model to work for new drugs and diseases, weighted [Formula see text] nearest neighbor was used as a preprocessing step to reconstruct the interaction score profiles of drugs with diseases. Finally, a graph regularized non-negative matrix factorization model was used to identify potential associations between drug and disease.

RESULTS:

During the cross-validation process, WNMFDDA achieved the AUC values of 0.939 and 0.952 on Fdataset and Cdataset under ten-fold cross validation, respectively, which outperforms other competing prediction methods. Moreover, case studies for several drugs and diseases were carried out to further verify the predictive performance of WNMFDDA. As a result, 13(Doxorubicin), 13(Amiodarone), 12(Obesity) and 12(Asthma) of the top 15 corresponding candidate diseases or drugs were confirmed by existing databases.

CONCLUSIONS:

The experimental results adequately demonstrated that WNMFDDA is a very effective method for drug-disease association prediction. We believe that WNMFDDA is helpful for relevant biomedical researchers in follow-up studies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Algoritmos Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Algoritmos Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article