Evidence map›Paper›PMID 38216907›Full record

ArticleBMC bioinformatics2024

DNI-MDCAP: improvement of causal MiRNA-disease association prediction based on deep network imputation.

Yu Han, Qiong Zhou, Leibo Liu, Jianwei Li, Yuan Zhou

Abstract read
In one paragraph

Article in BMC bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Yu Han *Department of Biomedical Informatics, School of Basic Medical Sciences, Peking University, Beijing, China.
Qiong Zhou *Department of Biomedical Informatics, School of Basic Medical Sciences, Peking University, Beijing, China.
Leibo LiuDepartment of Biomedical Informatics, School of Basic Medical Sciences, Peking University, Beijing, China.
Jianwei LiInstitute of Computational Medicine, School of Artificial Intelligence, Hebei University of Technology, Tianjin, China.
Yuan ZhouDepartment of Biomedical Informatics, School of Basic Medical Sciences, Peking University, Beijing, China. zhouyuanbioinfo@hsc.pku.edu.cn.

Funding

National Key Research and Development Program of China 2021YFF1201201National Natural Science Foundation of China 32222020National Natural Science Foundation of China 62072154
6 · The paper itself

Abstract

backgroundMiRNAs are involved in the occurrence and development of many diseases. Extensive literature studies have demonstrated that miRNA-disease associations are stratified and encompass ~ 20% causal associations. Computational models that predict causal miRNA-disease associations provide effective guidance in identifying novel interpretations of disease mechanisms and potential therapeutic targets. Although several predictive models for miRNA-disease associations exist, it is still challenging to discriminate causal miRNA-disease associations from non-causal ones. Hence, there is a pressing need to develop an efficient prediction model for causal miRNA-disease association prediction.

resultsWe developed DNI-MDCAP, an improved computational model that incorporated additional miRNA similarity metrics, deep graph embedding learning-based network imputation and semi-supervised learning framework. Through extensive predictive performance evaluation, including tenfold cross-validation and independent test, DNI-MDCAP showed excellent performance in identifying causal miRNA-disease associations, achieving an area under the receiver operating characteristic curve (AUROC) of 0.896 and 0.889, respectively. Regarding the challenge of discriminating causal miRNA-disease associations from non-causal ones, DNI-MDCAP exhibited superior predictive performance compared to existing models MDCAP and LE-MDCAP, reaching an AUROC of 0.870. Wilcoxon test also indicated significantly higher prediction scores for causal associations than for non-causal ones. Finally, the potential causal miRNA-disease associations predicted by DNI-MDCAP, exemplified by diabetic nephropathies and hsa-miR-193a, have been validated by recently published literature, further supporting the reliability of the prediction model.

conclusionsDNI-MDCAP is a dedicated tool to specifically distinguish causal miRNA-disease associations with substantially improved accuracy. DNI-MDCAP is freely accessible at http://www.rnanut.net/DNIMDCAP/ .

Indexed as

MicroRNAsAlgorithmsComputational BiologyGenetic Predisposition to DiseaseHumansReproducibility of ResultsMicroRNAsCausal miRNA-disease association predictionDeep graph embeddingmiRNAmiRNA-disease associationNetwork imputation

Identifiers

PMID38216907
PMCPMC10785389

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.