Linking gene expression to clinical outcomes in pediatric Crohn's disease using machine learning
Kevin A Chen1,2, Nina C Nishiyama1,3, Meaghan M Kennedy Ng1,3
1Center for Gastrointestinal Biology and Disease, University of North Carolina at Chapel Hill, 7314 Medical Biomolecular Research Building, 111 Mason Farm Road, Chapel Hill, NC, 27599, USA.
Insights
Machine learning models accurately predict pediatric Crohn's disease complications using gene expression. These models identify high-risk patients for strictures and surgery, improving treatment strategies.
Area of Science:
- Genomics
- Machine Learning
- Pediatric Gastroenterology
Background:
- Pediatric Crohn's disease (CD) often presents with severe disease and complications.
- Predicting future complications in pediatric CD is crucial for effective management.
Purpose of the Study:
- To develop machine learning models for predicting complications in pediatric CD.
- To utilize ileal and colonic gene expression data for risk prediction.
Main Methods:
- Gene expression data from 101 FFPE biopsies of treatment-naïve pediatric CD patients and controls.
- Differential gene expression analysis and machine learning modeling to predict strictures, remission, and surgery.
- Analysis of clinical outcomes alongside gene expression data.
Main Results:
- Machine learning models achieved high accuracy in predicting outcomes (AUROC 0.84 for strictures, 0.83 for remission, 0.75 for surgery).
- Downregulation of inflammation and extracellular matrix pathways observed in patients with strictures.
- Key prognostic genes for strictures (REG1A, MMP3, DUOX2) identified through predictive models.
Conclusions:
- Colonic gene expression is important for predicting pediatric CD outcomes.
- Machine learning models show significant potential for predicting complications in pediatric CD using FFPE tissue.
- This approach can aid in personalized treatment strategies for pediatric Crohn's disease.
Abstract:
Pediatric Crohn's disease (CD) is characterized by a severe disease course with frequent complications. We sought to apply machine learning-based models to predict risk of developing future complications in pediatric CD using ileal and colonic gene expression. Gene expression data was generated from 101 formalin-fixed, paraffin-embedded (FFPE) ileal and colonic biopsies obtained from treatment-naïve CD patients and controls. Clinical outcomes including development of strictures or fistulas and progression to surgery were analyzed using differential expression and modeled using machine learning. Differential expression analysis revealed downregulation of pathways related to inflammation and extra-cellular matrix production in patients with strictures. Machine learning-based models were able to incorporate colonic gene expression and clinical characteristics to predict outcomes with high accuracy. Models showed an area under the receiver operating characteristic curve (AUROC) of 0.84 for strictures, 0.83 for remission, and 0.75 for surgery. Genes with potential prognostic importance for strictures (REG1A, MMP3, and DUOX2) were not identified in single gene differential analysis but were found to have strong contributions to predictive models. Our findings in FFPE tissue support the importance of colonic gene expression and the potential for machine learning-based models in predicting outcomes for pediatric CD.
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