Validation of a pan-ELastography Machine-learning (ELM) score to predict clinically significant portal hypertension in compensated advanced chronic liver disease.
Abstract:
BACKGROUND
Clinically significant portal hypertension (CSPH) drives decompensation and mortality in advanced chronic liver disease (ACLD). Although non-selective β-blockers (NSBB) reduce risk, accurate identification of patients with CSPH requires invasive hepatic venous pressure gradient (HVPG) measurement. The non-invasive Baveno-VII CSPH criteria based on liver stiffness measurement (LSM) and platelet count (PLT)-yield 40-50% indeterminate ("gray-zone") results and vary across etiologies and elastography techniques. Spleen stiffness measurement (SSM) has been proposed to improve the accuracy of the Baveno-VII CSPH criteria. We developed and validated a machine-learning (ML) model integrating pan-elastographic LSM and SSM results with clinical variables to improve CSPH rule-out and rule-in accuracy while minimizing indeterminate cases.
METHODS
We analyzed 1,435 compensated ACLD patients with paired HVPG, LSM, SSM, and clinical parameters. LSM and SSM were obtained by vibration-controlled transient elastography (VCTE), two-dimensional shear-wave elastography (2D-SWE), or point-SWE (p-SWE). Models were trained (n=943) and internally validated (n=150) using harmonized LSM/SSM from different technologies and clinical variables (PLT, Child-Pugh, age, gender, etiology). Cut-offs were selected for 100% negative predictive value (NPV) to rule-out and 100% positive predictive value (PPV) to rule-in CSPH. External validation was conducted in 342 patients across seven centers, comparing ML performance against Baveno VII, Baveno-SSM single- and dual-cut-off criteria, and, in the VCTE subgroup, ANTICIPATE and NICER scores.
RESULTS
A Random Forest-based model based achieved the highest performance (external validation: AUC=0.91, Brier Score=0.13), with cut-offs≤0.45 (rule-out) and ≥0.60 (rule-in) yielding NPV=0.90 (95%C.I.0.84-0.94) and PPV=0.96 (95%C.I.0.92-0.98). The ML gray-zone was 12.3%, versus 47.9% (Baveno VII;p<0.001), 38.6% (Baveno-SSM-dual;p<0.001), and 19.6% (Baveno-SSM-single;p<0.05). In the VCTE external-validation subgroup (n=275), ELM achieved comparable rule-in performance to ANTICIPATE and NICER, while reducing the gray zone to 12.0% versus 41.1% and 41.8%, respectively.
CONCLUSIONS
The ELM Score outperformed current Baveno criteria and markedly reduced gray zones across elastography modalities, supporting broader, safer, and non-invasive identification of ACLD patients with HVPG-defined CSPH who may be candidates for NSBB therapy.
Copyright © 2026. Published by Elsevier B.V.
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Authors
- Milos Ajcevic |
- Francesco Azzaroli |
- Mislav Barisic-Jaman |
- Annalisa Berzigotti |
- Pik Eu Jason Chang |
- Antonio Colecchia |
- Luigi Colecchia |
- Lory Crocè |
- Elton Dajti |
- Laure Elkrief |
- José Ignacio Fortea |
- Mirella Fraquelli |
- Mauro Giuffrè |
- Ivica Grgurević |
- Masashi Hirooka |
- Sang Gyun Kim |
- Simone Kresevic |
- Sandro Kukic |
- Elba Llop |
- Giovanni Marasco |
- Yuly Mendoza |
- Sebastian Mueller |
- Fabio Piscaglia |
- Ángela Puente |
- Pierre-Emmanuel Rautou |
- Federico Ravaioli |
- Thomas Reiberger |
- Matteo Rosselli |
- Dennis L Shung |
- Horia Stefanescu |
- Kisung You |
- Romanas Zykus |
Elsevier ScienceFull Text Sources - subscription/membership/fee required
Journal Title: Journal of hepatology
Journal ISSN: 1600-0641
Journal ISO Abbreviation: J Hepatol
Publication Date: 2026-07-01
DOI: 10.1016/j.jhep.2026.06.032
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