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Updated: Feb 13, 2026

A Mouse Model of Chronic Liver Fibrosis for the Study of Biliary Atresia
Published on: February 3, 2023
Transient elastography is useful in diagnosing biliary atresia and predicting prognosis after hepatoportoenterostomy
Jia-Feng Wu1, Chee-Seng Lee2, Wen-Hsi Lin3
1Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.
Insights
Transient elastography (TE) aids biliary atresia (BA) diagnosis in infants. Liver stiffness measurement (LSM) predicts BA and post-surgery outcomes, including the need for liver transplantation (LT).
Area of Science:
- Pediatric Gastroenterology
- Hepatology
- Diagnostic Imaging
Background:
- Biliary atresia (BA) is a severe neonatal cholestatic liver disease.
- Accurate diagnosis and prediction of BA outcomes are crucial for timely intervention.
- Transient elastography (TE) is a non-invasive method to assess liver stiffness.
Purpose of the Study:
- To evaluate the utility of TE for diagnosing BA in cholestatic infants.
- To predict BA outcomes, including complications and the need for liver transplantation (LT).
Main Methods:
- Forty-eight cholestatic infants (9-87 days) underwent liver stiffness measurement (LSM) via TE.
- Liver histology and fibrosis grading (METAVIR score) were assessed in 36 subjects.
- Statistical analyses included ROC curve, odds ratio, and Cox proportional analysis.
Main Results:
- BA infants showed significantly higher LSM and METAVIR scores than non-BA infants.
- An LSM >7.7 kPa predicted BA with 80% sensitivity and 97% specificity (AUC=85.3%).
- Post-surgery LSM >16 kPa predicted higher need for LT in BA infants.
Conclusions:
- LSM assessment during cholestasis workup can facilitate BA diagnosis.
- Post-operative LSM may predict complications and the need for early LT in BA patients.
Abstract:
We investigated the utility of transient elastography (TE) for diagnosing biliary atresia (BA) in cholestatic infants and predicting the outcome of BA. Forty-eight cholestatic infants (9-87 days of age) with direct bilirubin level >1 mg/dL were enrolled. Liver stiffness measurement (LSM) by TE was performed during the cholestasis workup, and 15 subjects were diagnosed as BA. We assessed liver histology using liver biopsies from 36 subjects and graded fibrosis status using the METAVIR score. BA infants had significantly higher LSM values and METAVIR scores than non-BA cholestatic infants. A receiver operating characteristic (ROC) curve analysis showed that an LSM >7.7 kPa was predictive of BA among cholestatic infants (sensitivity = 80%; specificity = 97%; area under the curve [AUC] = 85.3%; P = 0.0001). Cholestatic infants with an LSM >7.7 kPa were more likely to be diagnosed with BA (odds ratio [OR] = 128; P < 0.001). Very early measurement of LSM after hepatoportoenterostomy (HPE) is associated with occurrence of thrombocytopenia, splenomegaly, and esophageal varices 6 months post-HPE. Five of the BA subjects were awaiting or had received liver transplantation (LT), and they had a significantly higher LSM measured 1 week post-HPE than that in the other BA subjects (26.0 vs. 10.8 kPa; P = 0.006). A Cox proportional analysis demonstrated that the need for LT was significantly higher in BA subjects with LSM >16 kPa measured 1 week post-HPE than other BA subjects (hazard ratio [HR] = 10.16; P = 0.04).
Conclusion:
LSM assessment during the workup of cholestatic infants may facilitate the diagnosis of BA. LSM post-HPE may predict complications and the need for early LT in infants with BA. (Hepatology 2018).
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