Validation of a pan-ELastography Machine-learning (ELM) score to predict clinically significant portal hypertension

Mauro Giuffrè1, Simone Kresevic2, Federico Ravaioli3

  • 1Department of Medical, Surgical, and Health Sciences, University of Trieste, Trieste, Italy.

Insights

A new machine learning (ML) model accurately identifies clinically significant portal hypertension (CSPH) in advanced chronic liver disease (ACLD) patients, reducing indeterminate cases and improving non-invasive diagnosis for potential non-selective beta-blocker (NSBB) therapy.

Area of Science:

  • Hepatology and Gastroenterology
  • Medical Imaging and Diagnostics
  • Machine Learning in Medicine

Background:

  • Clinically significant portal hypertension (CSPH) is a critical determinant of decompensation and mortality in advanced chronic liver disease (ACLD).
  • Current non-invasive criteria (Baveno-VII) for CSPH identification have limitations, including a high proportion of indeterminate ('gray-zone') results and variability across elastography techniques.
  • Spleen stiffness measurement (SSM) has shown promise in improving CSPH assessment, but integration with liver stiffness measurement (LSM) and clinical data is needed.

Purpose of the Study:

  • To develop and validate a machine-learning (ML) model integrating pan-elastographic LSM and SSM with clinical variables to enhance the accuracy of CSPH rule-out and rule-in.
  • To minimize the indeterminate ('gray-zone') results in identifying patients with CSPH compared to existing non-invasive criteria.
  • To support safer and broader non-invasive identification of ACLD patients eligible for non-selective beta-blocker (NSBB) therapy.

Main Methods:

  • Analysis of 1,435 compensated ACLD patients with paired hepatic venous pressure gradient (HVPG), LSM, SSM, and clinical parameters.
  • Harmonized LSM/SSM data from vibration-controlled transient elastography (VCTE), 2D-SWE, and point-SWE were integrated with clinical variables (platelet count, Child-Pugh score, age, gender, etiology) for model training and internal validation.
  • External validation in 342 patients compared the ML model's performance against Baveno-VII, Baveno-SSM criteria, and established scores (ANTICIPATE, NICER) in VCTE subgroups.

Main Results:

  • The developed Random Forest-based ML model (ELM Score) demonstrated high performance in external validation (AUC=0.91, Brier Score=0.13).
  • The ML model significantly reduced the gray zone to 12.3% compared to Baveno-VII (47.9%), Baveno-SSM-dual (38.6%), and Baveno-SSM-single (19.6%) criteria (p<0.001).
  • In the VCTE subgroup, the ELM Score achieved comparable rule-in performance to ANTICIPATE and NICER while further reducing the gray zone to 12.0%.

Conclusions:

  • The ELM Score, integrating multi-modal elastography and clinical data, significantly outperforms current Baveno criteria in identifying CSPH across different elastography techniques.
  • This ML-based approach markedly reduces indeterminate cases, enabling broader, safer, and non-invasive identification of ACLD patients with HVPG-defined CSPH.
  • The ELM Score supports improved patient selection for NSBB therapy, potentially improving outcomes in advanced chronic liver disease.
Abstract