AI Article Synopsis

  • Metabolomics plays a crucial role in identifying disease-related metabolites, aiding in disease diagnosis and understanding underlying mechanisms.
  • A new model called Disease and Literature Driven Metabolism Prediction Model (DLMPM) was developed to identify potential connections between metabolites and diseases, uncovering 1,406 direct associations and predicting over 119,000 unknown ones.
  • DLMPM demonstrates strong performance in predicting metabolic signatures for diseases, achieving an average AUC value of 82.33%, and outperforms previous methods, thus enhancing research on human diseases.

Article Abstract

Background: In biological systems, metabolomics can not only contribute to the discovery of metabolic signatures for disease diagnosis, but is very helpful to illustrate the underlying molecular disease-causing mechanism. Therefore, identification of disease-related metabolites is of great significance for comprehensively understanding the pathogenesis of diseases and improving clinical medicine.

Results: In the paper, we propose a disease and literature driven metabolism prediction model (DLMPM) to identify the potential associations between metabolites and diseases based on latent factor model. We build the disease glossary with disease terms from different databases and an association matrix based on the mapping between diseases and metabolites. The similarity of diseases and metabolites is used to complete the association matrix. Finally, we predict potential associations between metabolites and diseases based on the matrix decomposition method. In total, 1,406 direct associations between diseases and metabolites are found. There are 119,206 unknown associations between diseases and metabolites predicted with a coverage rate of 80.88%. Subsequently, we extract training sets and testing sets based on data increment from the database of disease-related metabolites and assess the performance of DLMPM on 19 diseases. As a result, DLMPM is proven to be successful in predicting potential metabolic signatures for human diseases with an average AUC value of 82.33%.

Conclusion: In this paper, a computational model is proposed for exploring metabolite-disease pairs and has good performance in predicting potential metabolites related to diseases through adequate validation. The results show that DLMPM has a better performance in prioritizing candidate diseases-related metabolites compared with the previous methods and would be helpful for researchers to reveal more information about human diseases.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8985251PMC
http://dx.doi.org/10.1186/s12864-022-08504-wDOI Listing

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