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©The Author(s) 2025.
World J Gastroenterol. Sep 28, 2025; 31(36): 112217
Published online Sep 28, 2025. doi: 10.3748/wjg.v31.i36.112217
Published online Sep 28, 2025. doi: 10.3748/wjg.v31.i36.112217
Table 1 Comparative performance and characteristics of non-invasive fibrosis scores in pediatric non-alcoholic fatty liver disease/metabolic dysfunction-associated steatotic liver disease
Key components | Target population | Reported AUROC for advanced fibrosis (F ≥ 3) | Ref. | |
CH-MASLD-Fib (machine learning model, hypothetical) | Multiple clinical and laboratory variables (machine learning-derived) | Pediatric (Chinese cohort) | Approximately 0.92 (derivation cohort) | Yao et al[1] |
NAFLD fibrosis score | Age, BMI, impaired fasting glucose/diabetes, AST/ALT ratio, platelet count, albumin | Adult (developed in adults) | No diagnostic ability (AUROC: Approximately 0.50; P = 0.14) | Angulo et al[8] |
FIB-4 index | Age, AST, ALT, platelet count | Adult (developed in adults) | Poor (AUROC range: Approximately 0.32-0.54) | Shah et al[9] |
AST to platelet ratio index | AST level, platelet count | Adult (developed in adults) | Fair for any fibrosis (AUROC range: Approximately 0.70-0.80); poor for advanced fibrosis (AUROC range: Approximately 0.50-0.60) | Chrysanthos et al[10] |
Pediatric NAFLD fibrosis score | ALT, alkaline phosphatase, platelet count, GGT | Pediatric (developed in children) | 0.74 (95%CI: 0.66-0.82) | Alkhouri et al[7] |
- Citation: Yodoshi T. Machine learning fibrosis score for pediatric metabolic dysfunction-associated steatotic liver disease: Promising but premature. World J Gastroenterol 2025; 31(36): 112217
- URL: https://www.wjgnet.com/1007-9327/full/v31/i36/112217.htm
- DOI: https://dx.doi.org/10.3748/wjg.v31.i36.112217