{"title":"CLHGNNMDA: Hypergraph Neural Network Model Enhanced by Contrastive Learning for miRNA-Disease Association Prediction.","authors":"Rong Zhu, Yong Wang, Ling-Yun Dai","doi":"10.1089/cmb.2024.0720","DOIUrl":null,"url":null,"abstract":"<p><p>Numerous biological experiments have demonstrated that microRNA (miRNA) is involved in gene regulation within cells, and mutations and abnormal expression of miRNA can cause a myriad of intricate diseases. Forecasting the association between miRNA and diseases can enhance disease prevention and treatment and accelerate drug research, which holds considerable importance for the development of clinical medicine and drug research. This investigation introduces a contrastive learning-augmented hypergraph neural network model, termed CLHGNNMDA, aimed at predicting associations between miRNAs and diseases. Initially, CLHGNNMDA constructs multiple hypergraphs by leveraging diverse similarity metrics related to miRNAs and diseases. Subsequently, hypergraph convolution is applied to each hypergraph to extract feature representations for nodes and hyperedges. Following this, autoencoders are employed to reconstruct information regarding the feature representations of nodes and hyperedges and to integrate various features of miRNAs and diseases extracted from each hypergraph. Finally, a joint contrastive loss function is utilized to refine the model and optimize its parameters. The CLHGNNMDA framework employs multi-hypergraph contrastive learning for the construction of a contrastive loss function. This approach takes into account inter-view interactions and upholds the principle of consistency, thereby augmenting the model's representational efficacy. The results obtained from fivefold cross-validation substantiate that the CLHGNNMDA algorithm achieves a mean area under the receiver operating characteristic curve of 0.9635 and a mean area under the precision-recall curve of 0.9656. These metrics are notably superior to those attained by contemporary state-of-the-art methodologies.</p>","PeriodicalId":15526,"journal":{"name":"Journal of Computational Biology","volume":" ","pages":"47-63"},"PeriodicalIF":1.4000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Computational Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1089/cmb.2024.0720","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/27 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
Numerous biological experiments have demonstrated that microRNA (miRNA) is involved in gene regulation within cells, and mutations and abnormal expression of miRNA can cause a myriad of intricate diseases. Forecasting the association between miRNA and diseases can enhance disease prevention and treatment and accelerate drug research, which holds considerable importance for the development of clinical medicine and drug research. This investigation introduces a contrastive learning-augmented hypergraph neural network model, termed CLHGNNMDA, aimed at predicting associations between miRNAs and diseases. Initially, CLHGNNMDA constructs multiple hypergraphs by leveraging diverse similarity metrics related to miRNAs and diseases. Subsequently, hypergraph convolution is applied to each hypergraph to extract feature representations for nodes and hyperedges. Following this, autoencoders are employed to reconstruct information regarding the feature representations of nodes and hyperedges and to integrate various features of miRNAs and diseases extracted from each hypergraph. Finally, a joint contrastive loss function is utilized to refine the model and optimize its parameters. The CLHGNNMDA framework employs multi-hypergraph contrastive learning for the construction of a contrastive loss function. This approach takes into account inter-view interactions and upholds the principle of consistency, thereby augmenting the model's representational efficacy. The results obtained from fivefold cross-validation substantiate that the CLHGNNMDA algorithm achieves a mean area under the receiver operating characteristic curve of 0.9635 and a mean area under the precision-recall curve of 0.9656. These metrics are notably superior to those attained by contemporary state-of-the-art methodologies.
期刊介绍:
Journal of Computational Biology is the leading peer-reviewed journal in computational biology and bioinformatics, publishing in-depth statistical, mathematical, and computational analysis of methods, as well as their practical impact. Available only online, this is an essential journal for scientists and students who want to keep abreast of developments in bioinformatics.
Journal of Computational Biology coverage includes:
-Genomics
-Mathematical modeling and simulation
-Distributed and parallel biological computing
-Designing biological databases
-Pattern matching and pattern detection
-Linking disparate databases and data
-New tools for computational biology
-Relational and object-oriented database technology for bioinformatics
-Biological expert system design and use
-Reasoning by analogy, hypothesis formation, and testing by machine
-Management of biological databases