Prediction of Disease Comorbidity Using HeteSim Scores based on Multiple Heterogeneous Networks

Curr Gene Ther. 2019;19(4):232-241. doi: 10.2174/1566523219666190917155959.

Abstract

Background: Accumulating experimental studies have indicated that disease comorbidity causes additional pain to patients and leads to the failure of standard treatments compared to patients who have a single disease. Therefore, accurate prediction of potential comorbidity is essential to design more efficient treatment strategies. However, only a few disease comorbidities have been discovered in the clinic.

Objective: In this work, we propose PCHS, an effective computational method for predicting disease comorbidity.

Materials and methods: We utilized the HeteSim measure to calculate the relatedness score for different disease pairs in the global heterogeneous network, which integrates six networks based on biological information, including disease-disease associations, drug-drug interactions, protein-protein interactions and associations among them. We built the prediction model using the Support Vector Machine (SVM) based on the HeteSim scores.

Results and conclusion: The results showed that PCHS performed significantly better than previous state-of-the-art approaches and achieved an AUC score of 0.90 in 10-fold cross-validation. Furthermore, some of our predictions have been verified in literatures, indicating the effectiveness of our method.

Keywords: Disease comorbidity; HeteSim measure; disease drug; disease gene; heterogeneous network; protein-protein interaction..

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms
  • China / epidemiology
  • Comorbidity
  • Computational Biology / methods*
  • Drug Interactions*
  • Female
  • Humans
  • Lung Neoplasms / drug therapy
  • Lung Neoplasms / epidemiology*
  • Lung Neoplasms / metabolism
  • Lung Neoplasms / pathology
  • Models, Statistical
  • Ovarian Neoplasms / drug therapy
  • Ovarian Neoplasms / epidemiology*
  • Ovarian Neoplasms / metabolism
  • Ovarian Neoplasms / pathology
  • Prevalence
  • Protein Interaction Maps*