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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*
  • *Corresponding author for this work
  • Faculty of Computing, Harbin Institute of Technology
  • Harbin Institute of Technology
  • Beidahuang Industry Group General Hospital
  • Beidahuang Group Neuropsychiatric Prevention and Treatment Hospital

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish
Article numbere70572
JournalAging Cell
Volume25
Issue number6
DOIs
StatePublished - Jun 2026

Keywords

  • age-related diseases
  • aging
  • dual GCNs
  • hypertension
  • lncRNA marker

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