Integrative bioinformatics analysis and experimental validation of key biomarkers for risk stratification in primary biliary cholangitis

Arthritis Res TherPublished Integrative bioinformatics analysis with experimental validation

Authors' conclusion

In summary, combining bioinformatics analysis and experiment validation, we identified TXNIP, CD44, and ENTPD1 as promising biomarkers for risk stratification in PBC patients.

Study context

Population
Patients with primary biliary cholangitis (PBC)
Outcome
Identification of patients at risk of disease progression (risk stratification)
Methodological detailsGene Expression Omnibus (GEO) microarray datasets, validation in public datasets and PBC mouse model, validation in clinical serum samples
  • GEO microarray datasets
  • Validation in public datasets and PBC mouse model
  • Validation in clinical serum samples

Performance

As reported in the abstract

Identification of patients at risk of disease progression
Test or modelAUC95% CI
Three-gene panel0.7770.657-0.870

Three-gene panel

AUC0.777
95% CI0.657-0.870

Further findings

Differentially expressed genes (DEGs) in the GSE79850 dataset

DEGs identified
166
Upregulated genes
95
Downregulated genes
71
DEGs significantly enriched in inflammatory or immune-related process

Risk-related genes

Risk-related genes recognised and validated in GSE119600 cohort
15
Candidate hub genes: TXNIP, CD44, ENTPD1, PDGFRB
4

Original publication

Integrative bioinformatics analysis and experimental validation of key biomarkers for risk stratification in primary biliary cholangitis. Arthritis Res Ther. Published 2 October 2023. doi:10.1186/s13075-023-03163-y

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