Evidence map›Paper›PMID 42460394›Full record

ArticleFrontiers in bioinformatics2026

A multi-scale biological network framework for discovering MiRNA-Disease associations.

Zhang Yu, Zuo Xuan, Tang Ying, Jiang Shanshan, Qian Kun, Li Linkai, Zhou Zihao, Hong Xiuqin, Liu Zhengyu, Pan Hongwei

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Article in Frontiers in bioinformatics, 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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5 · Who and what money

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10 authors.

Zhang Yu *Cardiology Department, Hunan Provincial People's Hospital, Changsha, China.
Zuo Xuan *The First Affiliated Hospital of Hunan Normal University, Changsha, China.
Tang YingThe First Affiliated Hospital of Hunan Normal University, Changsha, China.
Jiang ShanshanThe First Affiliated Hospital of Hunan Normal University, Changsha, China.
Qian KunThe First Affiliated Hospital of Hunan Normal University, Changsha, China.
Li LinkaiThe First Affiliated Hospital of Hunan Normal University, Changsha, China.
Zhou ZihaoSchool of Information Science and Engineering, Guilin University of Technology, Guilin, China.
Hong XiuqinThe First Affiliated Hospital of Hunan Normal University, Changsha, China.
Liu ZhengyuCardiology Department, Hunan Provincial People's Hospital, Changsha, China.
Pan HongweiCardiology Department, Hunan Provincial People's Hospital, Changsha, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Identifying potential miRNA-disease associations is essential for clarifying the molecular basis of complex diseases and accelerating the discovery of diagnostic biomarkers and therapeutic targets. However, the performance of existing computational methods is often limited by sparse biological interaction networks, highly imbalanced disease distributions, and the small number of experimentally validated associations. Methods: To address these challenges, we propose MMAG, a novel framework that formulates miRNA-disease association prediction as a meta-conditional distribution alignment problem on multi-scale biological graphs. MMAG integrates three complementary components. First, a multi-scale representation learning module captures hierarchical biological information from local topological connectivity, mesoscopic functional organization, and global spectral structure. Second, a meta-learning strategy models each disease as an individual task, enabling the model to learn disease-specific prototype representations from support samples and adapt effectively to few-shot settings. Third, a conditional adversarial alignment mechanism reduces feature distribution discrepancies across diseases with different data scales, thereby enhancing cross-task knowledge transfer and generalization. Results: Extensive experiments demonstrate that MMAG consistently outperforms several state-of-the-art methods under few-shot, long-tailed, and cross-dataset transfer scenarios. Discussion: These results indicate that MMAG provides an effective and scalable solution for miRNA-disease association prediction and offers a promising strategy for broader biological network inference tasks.

Indexed as

biological graphsdeep learningmeta-learningmiRNA-diseasemulti-scale

Identifiers

PMID42460394
PMCPMC13368795

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