ArticlePloS one2025
Revealing potential interfering genes between abdominal aortic aneurysm and periodontitis through machine learning and bioinformatics analysis.
Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.
What it found
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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.
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.
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Who cites it
1 citing paper in PubMed, 1 synthesis or guideline pooled it.
Corrections and comments
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Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
This study aimed to identify potential interacting genes between abdominal aortic aneurysm (AAA) and periodontitis. To achieve this, we obtained datasets of AAA and periodontitis from the GEO database, conducted differential analysis on the AAA dataset, and performed weighted gene co-expression network analysis (WGCNA) on the periodontitis dataset to preliminarily identify interacting genes via intersection. Subsequently, we refined key candidate genes by constructing a PPI network and applying three machine learning algorithms. These candidate genes were further validated through external independent datasets, receiver operating characteristic (ROC) curves, and Nomograms. Finally, single-gene Gene Set Enrichment Analysis (GSEA), immune landscape analysis, and targeted drug prediction were performed on the identified key genes. In our study, a total of 323 differentially expressed genes (DEGs) related to AAA and 4,412 periodontitis-related module genes were identified, producing 90 interacting genes through intersection initially. Through PPI network analysis and machine learning, we prioritized 7 key interacting genes. Validation confirmed that IL1B, PTGS2, and SELL were robustly associated with both diseases. Immune landscape assessment demonstrated that these three genes exhibited significant negative correlations with regulatory T cells (Tregs) and positive correlations with neutrophil infiltration. Additionally, ten drugs with the highest predicted target specificity were identified. In conclusion, we utilized various machine learning and bioinformatics approaches to preliminarily elucidate potential comorbid mechanisms between AAA and periodontitis from a multidisciplinary perspective.
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Registered trials
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