A 6 gene signature identifies the risk of developing cirrhosis in patients with chronic hepatitis B

Ming-Yi Xu1, Ying Qu1, Zhenghong Li1

  • 1Department of Gastroenterology, Shanghai First People's Hospital, Shanghai Jiao Tong University, Shanghai, 200080, China.

Insights

A new Cirrhosis Risk Score (CRS) using six predictor genes accurately identifies cirrhosis risk in chronic hepatitis B (CHB) patients. This gene signature offers a more reliable prediction than clinical factors, potentially reducing liver biopsies.

Area of Science:

  • Hepatology
  • Genomics
  • Biomarker Discovery

Background:

  • Clinical factors and liver biopsy have limitations in predicting cirrhosis risk in chronic hepatitis B (CHB).
  • Accurate risk stratification is crucial for managing CHB and preventing disease progression.

Purpose of the Study:

  • To develop and validate a predictive gene signature for cirrhosis risk in untreated CHB patients.
  • To create a Cirrhosis Risk Score (CRS) based on selected predictor genes.
  • To evaluate the efficacy of the CRS compared to clinical factors.

Main Methods:

  • Gene expression profiling using GeneChip on liver tissues from 183 untreated CHB patients.
  • Identification of significant predictor genes (PGs) using Significant Analysis of Microarray (SAM) and Prediction Analysis of Microarray (PAM).
  • Development and validation of a 6-gene signature (CD24, CXCL6, EHF, ITGBL1, LUM, SOX9) and calculation of the CRS.

Main Results:

  • A 6-gene signature was developed, forming the basis for the Cirrhosis Risk Score (CRS).
  • The CRS demonstrated a high predictive value with an area under the ROC curve (AUROC) of 0.944.
  • The CRS outperformed both individual predictor genes and clinical factors in differentiating cirrhosis risk.

Conclusions:

  • The developed Cirrhosis Risk Score (CRS) is a superior predictor of cirrhosis risk in CHB patients compared to traditional clinical factors.
  • Implementing the CRS in clinical practice can aid in better patient stratification and potentially reduce the need for invasive liver biopsies.

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