Evidence map›Paper›PMID 42265541›Full record

ArticleAging cell2026

iLDA-SGCN: Identifying Associations Between Age-Related Diseases and Long Non-Coding RNAs Using Dual Graph Convolutional Networks.

Yu Guo, Shizheng Qiu, Zhishuai Zhang, Jirui Guo, Haozheng Liang, Huanyu You, Fengjuan Lu, Yanwei Xu, Yang Hu

Abstract read
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Article in Aging cell, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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9 authors.

Yu GuoCenter for Bioinformatics, Faculty of Computing, Harbin Institute of Technology, Harbin, China.
Shizheng QiuCenter for Bioinformatics, Faculty of Computing, Harbin Institute of Technology, Harbin, China.ORCID https://orcid.org/0000-0002-0047-4199
Zhishuai ZhangCenter for Bioinformatics, Faculty of Computing, Harbin Institute of Technology, Harbin, China.
Jirui GuoCenter for Bioinformatics, Faculty of Computing, Harbin Institute of Technology, Harbin, China.
Haozheng LiangCenter for Bioinformatics, Faculty of Computing, Harbin Institute of Technology, Harbin, China.
Huanyu YouCenter for Bioinformatics, Faculty of Computing, Harbin Institute of Technology, Harbin, China.
Fengjuan LuBeidahuang Industry Group General Hospital, Harbin, China.
Yanwei XuBeidahuang Group Neuropsychiatric Prevention and Treatment Hospital, Harbin, China.
Yang HuCenter for Bioinformatics, Faculty of Computing, Harbin Institute of Technology, Harbin, China.ORCID https://orcid.org/0000-0002-4508-5365

Funding

0-1 Original Exploration Category: Fundamental Research Funds for the Central Universities Project 2022FRFK030025Heilongjiang Provincial Science and Technology Tackling Project GNCMSSJH2024National Natural Science Foundation of China 62371161Research and Innovation Fund of The First Affiliated Hospital of Harbin Medical University 2021M13
6 · The paper itself

Abstract

Aging reshapes global disease burdens, yet the regulatory roles of long non-coding RNAs (lncRNAs) in age-related disorders remain incompletely characterized. We developed iLDA-SGCN, a graph-based computational framework that integrates singular value decomposition (SVD) with dual graph convolutional networks (GCNs) to predict lncRNA-disease associations. SVD first derives compact low-dimensional representations from the lncRNA-disease association matrix. Two complementary GCN modules then learn topology-aware embeddings: a correlation-map GCN operating on the bipartite lncRNA-disease network, and a similarity-map GCN operating on fused homogeneous graphs of lncRNAs and diseases constructed from MeSH semantic similarity and Gaussian association-profile kernels. Finally, association scores are estimated with an inner-product decoder optimized with a class-imbalance-aware loss function. Across five-fold cross-validation on LncRNADisease and MNDR datasets, iLDA-SGCN outperformed five competitive methods (SDLDA, LDNFSGB, IPCARF, LDASR, and LDA-VGHB) in terms of AUC (area under the ROC curve) and AUPR (area under the precision-recall curve). The model achieved AUC/AUPR of 0.960/0.968 on MNDR and 0.896/0.901 on LncRNADisease, with only a marginal precision shortfall versus LDA-VGHB on LncRNADisease. Ablation studies showed both GCN modules improved over a fully connected backbone, with the similarity-map GCN contributing the largest gains; the full model performed best overall. In case studies across eight prototypical age-related diseases, iLDA-SGCN identified HOTAIR, MALAT1, PVT1, MEG3, H19, LSINCT5, UCA1, and other candidates, yielding 33 candidates potentially involved in age-related disease mechanisms that require further experimental validation. Collectively, iLDA-SGCN integrates semantic and topological information to prioritize candidate lncRNA-disease associations related to aging, providing testable hypotheses for downstream mechanistic studies.

Indexed as

AgingRNA, Long NoncodingGraph Neural NetworksHumansRNA, Long Noncodingage‐related diseasesagingdual GCNshypertensionlncRNA marker

Identifiers

PMID42265541
PMCPMC13249584

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