# Fast graph convolutional models incorporating matrix factorization for predicting microbe-disease associations

**Authors:** Qingwen Wu, Sujuan Tang

PMC · DOI: 10.1038/s41598-025-30284-y · Scientific Reports · 2025-12-10

## TL;DR

This paper introduces a new computational method to predict which microbes are associated with specific diseases, using graph convolution and matrix factorization techniques.

## Contribution

The novel contribution is the integration of fast graph convolution and matrix factorization for improved microbe-disease association prediction.

## Key findings

- FGCNMF outperforms existing state-of-the-art methods on benchmark datasets.
- The method uses enhanced node embeddings from a combined microbe-disease network for accurate predictions.

## Abstract

Revealing the relationship between microbe and disease is of great significance to the diagnosis, treatment, and prevention of disease. To overcome the expensive cost and trial-and-error settings, a series of in-silico methods have been proposed to predict microbe-disease association. However, the predictive performance of the current methods is modest. In this paper, we propose a new computational method based on Fast Graph Convolutional and Matrix Factorization, called FGCNMF, which addresses microbe-disease association prediction as a binary classification task by learning embedding representation of nodes on a microbe-disease network. We integrate background information from both microbe and disease spaces into the same global network framework, and use the randomized Singular Value Decomposition algorithm to obtain high-quality initial embedding representations of node. Then, Fast Spatial Convolution is implemented to enhance the embedding representations. Finally, using the enhanced representation of node pairs as input, and using Extra-Trees classifier to predict the final label. Experimental results demonstrate that FGCNMF has improved performance in comparison with other state-of-the-art computational methods on the benchmark datasets.

## Full-text entities

- **Genes:** MFSD11 (major facilitator superfamily domain containing 11) [NCBI Gene 79157] {aka ET}
- **Diseases:** IBD (MESH:D015212), Asthma (MESH:D001249), obesity (MESH:D009765), gut microbiome (MESH:C536735), inflammatory disease (MESH:D007249), guttate psoriasis (MESH:D011565), atherosclerosis (MESH:D050197), atopic dermatitis (MESH:D003876), diabetes (MESH:D003920), non-alcoholic fatty liver disease (MESH:D065626), cardiometabolic disorders (MESH:D024821), immunological dysfunction (MESH:D007154), dysbiosis (MESH:D064806)
- **Chemicals:** FGCNMF (-), short-chain fatty acids (MESH:D005232)
- **Species:** Staphylococcus aureus (species) [taxon 1280], Streptococcus pyogenes (species) [taxon 1314], Homo sapiens (human, species) [taxon 9606], Odoribacter (genus) [taxon 283168]

## Full text

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## Figures

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## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC12780053/full.md

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Source: https://tomesphere.com/paper/PMC12780053