Cited by 260Liver Disease and TransplantationLiver Disease Diagnosis and TreatmentLiver Diseases and Immunity

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Noninvasive Diagnosis of Portal Hypertension in Patients With Compensated Advanced Chronic Liver Disease

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Pons, Monica, Augustin, Salvador, Scheiner, Bernhard, Guillaume, Maeva, Rosselli, Matteo, Rodrigues, Susana G., Stefanescu, Horia, Ma, Mang M., Mandorfer, Mattias, Mergeay-Fabre, Mayka, Procopet, Bogdan, Schwabl, Philipp, Ferlitsch, Arnulf, Semmler, Georg, Berzigotti, Annalisa, Tsochatzis, Emmanuel, Bureau, Christophe, Reiberger, Thomas, Bosch, Jaime, Abraldes, Juan G., Genescà, Joan·2021·American Journal of Gastroenterology

Abstract

INTRODUCTION: We aimed to explore the prevalence of portal hypertension in the most common etiologies of patients with compensated advanced chronic liver disease (cACLD) and develop classification rules, based on liver stiffness measurement (LSM), that could be readily used to diagnose or exclude clinically significant portal hypertension (CSPH) in clinical practice. METHODS: This is an international cohort study including patients with paired LSM/hepatic venous pressure gradient (HVPG), LSM ≥10 kPa, and no previous decompensation. Portal hypertension was defined by an HVPG >5 mm Hg. A positive predictive value ≥90% was considered to validate LSM cutoffs for CSPH (HVPG ≥10 mm Hg), whereas a negative predictive value ≥90% ruled out CSPH. RESULTS: A total of 836 patients with hepatitis C (n = 358), nonalcoholic steatohepatitis (NASH, n = 248), alcohol use (n = 203), and hepatitis B (n = 27) were evaluated. Portal hypertension prevalence was >90% in all cACLD etiologies, except for patients with NASH (60.9%), being even lower in obese patients with NASH (53.3%); these lower prevalences of portal hypertension in patients with NASH were maintained across different strata of LSM values. LSM ≥25 kPa was the best cutoff to rule in CSPH in alcoholic liver disease, chronic hepatitis B, chronic hepatitis C, and nonobese patients with NASH, whereas in obese NASH patients, the positive predictive value was only 62.8%. A new model for patients with NASH (ANTICIPATE-NASH model) to predict CSPH considering body mass index, LSM, and platelet count was developed, and a nomogram was constructed. LSM ≤15 kPa plus platelets ≥150 × 10/L ruled out CSPH in most etiologies. DISCUSSION: Patients with cACLD of NASH etiology, especially obese patients with NASH, present lower prevalences of portal hypertension compared with other cACLD etiologies. LSM ≥25 kPa is sufficient to rule in CSPH in most etiologies, including nonobese patients with NASH, but not in obese patients with NASH.

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Authors
Pons, M., Augustin, S., Scheiner, B., Guillaume, M., Rosselli, M., Rodrigues, S. G., Stefanescu, H., Ma, M. M., Mandorfer, M., Mergeay-Fabre, M., Procopet, B., Schwabl, P., Ferlitsch, A., Semmler, G., Berzigotti, A., Tsochatzis, E., Bureau, C., Reiberger, T., Bosch, J., Abraldes, J. G., & Genescà, J.
Affiliations
  • Liver Unit, Department of Internal Medicine, Hospital Universitari Vall d'Hebron, Vall d'Hebron Institut de Recerca (VHIR), Faculty of Medicine, Universitat Autònoma de Barcelona, Barcelona, Spain;
  • Medical University of Vienna (AT)
  • Service d'Hépatologie CHU Toulouse Rangueil, Institut Cardiomet et Université Paul Sabatier, Toulouse, France;
  • The Royal Free Hospital (GB)
  • University of Bern (CH)
  • Liver Unit, Regional Institute of Gastroenterology and Hepatology “Octavian Fodor,” University of Medicine and Pharmacy “Iuliu Hatieganu,” Cluj-Napoca, Romania;
  • University of Alberta (CA)
  • Université Toulouse III - Paul Sabatier (FR)
  • Hospital of the Brothers of St. John of God (AT)
  • Division of Gastroenterology (Liver Unit), University of Alberta, Edmonton, Canada;
  • Universitat Autònoma de Barcelona (ES)
Corresponding author
Genescà, Joan
Venue
American Journal of Gastroenterology
Published
2020-10-08
Volume
116
Issue
4
Pages
723-732
ISSN
  • 0002-9270 (ISSN-L)
  • 1572-0241
OpenAlex
W3092352032
Cited by
260
References
27
Citations by year
2026: 39 · 2025: 55 · 2024: 58 · 2023: 48 · 2022: 42 · 2021: 17 · 2020: 1
FWCI
15.87
Type
journal article
Language
en
Open access
Locations
  • The American Journal of Gastroenterology (publishedVersion)
  • PubMed (publishedVersion)
  • UCL Discovery (University College London) (submittedVersion)
  • HAL (submittedVersion)
  • Bern Open Repository and Information System (University of Bern) (submittedVersion)
Funders
Instituto de Salud Carlos III (PI17/00310, PI18/00947)
Topics
  • Health Sciences › Medicine › Hepatology › Liver Disease and Transplantation
  • Health Sciences › Medicine › Hepatology › Liver Disease Diagnosis and Treatment
  • Health Sciences › Medicine › Hepatology › Liver Diseases and Immunity
Keywords
portal hypertension, compensated advanced chronic liver disease, liver stiffness measurement, hepatic venous pressure gradient, nonalcoholic steatohepatitis, obesity, hepatitis C, alcoholic liver disease, chronic hepatitis B, nomogram, platelet count, non-invasive diagnosis, prevalence
MeSH terms
Aged, Female, Humans, Hypertension, Portal, Liver, Liver Cirrhosis, Male, Middle Aged, Predictive Value of Tests, Severity of Illness Index, Portal Pressure, Elasticity Imaging Techniques

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