Evidence map›Paper›PMID 41050112›Full record

ArticleJournal of pharmaceutical analysis2025

Multi-scale information fusion and decoupled representation learning for robust microbe-disease interaction prediction.

Wentao Wang, Qiaoying Yan, Qingquan Liao, Xinyuan Jin, Yinyin Gong, Linlin Zhuo, Xiangzheng Fu, Dongsheng Cao

Abstract read
In one paragraph

Article in Journal of pharmaceutical analysis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Wentao WangSchool of Data Science and Artificial Intelligence, Wenzhou University of Technology, Wenzhou, Zhejiang, 325027, China.
Qiaoying YanSchool of Data Science and Artificial Intelligence, Wenzhou University of Technology, Wenzhou, Zhejiang, 325027, China.
Qingquan LiaoCollege of Computer Science and Electronic Engineering, Hunan University, 410012, Changsha, China.
Xinyuan JinSchool of Data Science and Artificial Intelligence, Wenzhou University of Technology, Wenzhou, Zhejiang, 325027, China.
Yinyin GongCollege of Computer Science and Electronic Engineering, Hunan University, 410012, Changsha, China.
Linlin ZhuoSchool of Data Science and Artificial Intelligence, Wenzhou University of Technology, Wenzhou, Zhejiang, 325027, China.
Xiangzheng FuCollege of Computer Science and Electronic Engineering, Hunan University, 410012, Changsha, China.
Dongsheng CaoDepartment of Xiangya School of Pharmaceutical Sciences, Central South University, Changsha, 410003, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Research indicates that microbe activity within the human body significantly influences health by being closely linked to various diseases. Accurately predicting microbe-disease interactions (MDIs) offers critical insights for disease intervention and pharmaceutical research. Current advanced AI-based technologies automatically generate robust representations of microbes and diseases, enabling effective MDI predictions. However, these models continue to face significant challenges. A major issue is their reliance on complex feature extractors and classifiers, which substantially diminishes the models' generalizability. To address this, we introduce a novel graph autoencoder framework that utilizes decoupled representation learning and multi-scale information fusion strategies to efficiently infer potential MDIs. Initially, we randomly mask portions of the input microbe-disease graph based on Bernoulli distribution to boost self-supervised training and minimize noise-related performance degradation. Secondly, we employ decoupled representation learning technology, compelling the graph neural network (GNN) to independently learn the weights for each feature subspace, thus enhancing its expressive power. Finally, we implement multi-scale information fusion technology to amalgamate the multi-layer outputs of GNN, reducing information loss due to occlusion. Extensive experiments on public datasets demonstrate that our model significantly surpasses existing top MDI prediction models. This indicates that our model can accurately predict unknown MDIs and is likely to aid in disease discovery and precision pharmaceutical research. Code and data are accessible at: https://github.com/shmildsj/MDI-IFDRL.

Indexed as

AI-Based technologiesDecoupled representation learningMicrobe-disease interactions (MDIs)Multi-scale information fusionPharmaceutical research

Identifiers

PMID41050112
PMCPMC12491710

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.