Machine learning liver histology scores correlate with portal hypertension assessments in nonalcoholic steatohepatitis cirrhosis

Author:

Noureddin Mazen1ORCID,Goodman Zachary2,Tai Dean3,Chng Elaine L. K.3,Ren Yayun3,Boudes Pol4,Shlevin Harold4,Garcia‐Tsao Guadalupe5ORCID,Harrison Stephen A.6,Chalasani Naga P.7ORCID

Affiliation:

1. Houston Methodist Hospital and Houston Research Institute Houston Texas USA

2. Inova Fairfax Hospital Falls Church Virginia USA

3. HistoIndex Pte. Ltd. Singapore Singapore

4. Galectin Therapeutics Inc. Norcross USA

5. Section of Digestive Diseases Yale University and CT‐VA Healthcare System New Haven Connecticut USA

6. Pinnacle Clinical Research San Antonio Texas USA

7. Division of Gastroenterology and Hepatology, Department of Medicine Indiana University School of Medicine Indianapolis Indiana USA

Abstract

SummaryBackground and AimsIn cirrhotic nonalcoholic steatohepatitis (NASH) clinical trials, primary efficacy endpoints have been hepatic venous pressure gradient (HVPG), liver histology and clinical liver outcomes. Important histologic features, such as septa thickness, nodules features and fibrosis area have not been included in the histologic assessment and may have important clinical relevance. We assessed these features with a machine learning (ML) model.MethodsNASH patients with compensated cirrhosis and HVPG ≥6 mm Hg (n = 143) from the Belapectin phase 2b trial were studied. Liver biopsies, HVPG measurements and upper endoscopies were performed at baseline and at end of treatment (EOT). A second harmonic generation/two‐photon excitation fluorescence provided an automated quantitative assessment of septa, nodules and fibrosis (SNOF). We created ML scores and tested their association with HVPG, clinically significant HVPG (≥10 mm Hg) and the presence of varices (SNOF‐V).ResultsWe derived 448 histologic variables (243 related to septa, 21 related to nodules and 184 related to fibrosis). The SNOF score (≥11.78) reliably distinguished CSPH at baseline and in the validation cohort (baseline + EOT) [AUC = 0.85 and 0.74, respectively]. The SNOF‐V score (≥0.57) distinguished the presence of varices at baseline and in the same validation cohort [AUC = 0.86 and 0.73, respectively]. Finally, the SNOF‐C score differentiated those who had >20% change in HVPG against those who did not, with an AUROC of 0.89.ConclusionThe ML algorithm accurately predicted HVPG, CSPH, the development of varices and HVPG changes in patients with NASH cirrhosis. The use of ML histology model in NASH cirrhosis trials may improve the assessment of key outcome changes.

Publisher

Wiley

Subject

Pharmacology (medical),Gastroenterology,Hepatology

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