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Published on: February 19, 2019
Development a novel nomogram model for predicting significant hepatic histological changes in chronic hepatitis B
Na-Ling Kang1,2, Ya-Hong Gao3, Meng-Xin Lin4
1Department of Hepatology, Clinical Research Center for Liver and Intestinal Diseases of Fujian Province, Hepatology Research Institute, The First Affiliated Hospital, Fujian Medical University, Fujian, China.
A new nomogram model, HBGP, accurately identifies significant liver histological changes in chronic hepatitis B virus (HBV) carriers with normal ALT levels. This tool aids in deciding antiviral treatment for HBV patients.
Area of Science:
- Hepatology
- Virology
- Biostatistics
Background:
- Chronic hepatitis B virus (HBV) infection affects millions globally.
- Some HBV carriers with normal alanine transaminase (ALT) levels exhibit significant liver histological changes (SLHC).
- Accurate, noninvasive identification of SLHC is crucial for timely treatment decisions.
Purpose of the Study:
- To develop and validate a noninvasive nomogram model for identifying SLHC in chronic HBV carriers with normal ALT.
- To assess the model's performance across different upper limits of normal (ULNs) for ALT.
Main Methods:
- A training cohort of 732 chronic HBV carriers and an external validation cohort of 277 chronic HBV carriers were analyzed.
- Logistic regression and least absolute shrinkage and selection operator (LASSO) analyses were used.
- A nomogram model, HBGP, was constructed using hepatitis B surface antigen, gamma-glutamyl transpeptidase, and platelet count.
Main Results:
- The HBGP nomogram demonstrated strong predictive performance for SLHC, with an AUC of 0.866 in the training cohort and 0.885 in the validation cohort.
- High diagnostic values (AUCs ranging from 0.853 to 0.868) were observed across different ALT ULN strata.
- HBGP outperformed existing predictors in identifying SLHC.
Conclusions:
- The HBGP nomogram is a reliable, noninvasive tool for predicting SLHC in chronic HBV carriers with normal ALT.
- This model can assist clinicians in making informed decisions regarding the initiation of antiviral therapy.
- Further validation in diverse populations may enhance its clinical utility.
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