Evidence map›Paper›PMID 40922677›Full record

ArticleAlimentary pharmacology & therapeutics2026

Prediction of Hepatocellular Carcinoma and Other Liver-Related Events in Chronic Hepatitis B Patients With Metabolic Dysfunction or Metabolic Dysfunction-Associated Steatotic Liver Disease.

Lesley A Patmore, Ivana Carey, Jordan J Feld, Willem P Brouwer, Keyur Patel, Maria Buti, Pieter Honkoop, Douwe F Postma, Hans Blokzijl, Özgur M Koc and 13 more

Abstract readMulticenter Study
In one paragraph

Article in Alimentary pharmacology & therapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Trends in Comorbidities and Fatalities Among First-Time Hepatitis B Hospitalizations in Poland (2012-2023).Medical science monitor : international medical journal of experimental and clinical research · 2026
    Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors.

Lesley A PatmoreDepartment of Gastroenterology and Hepatology, Erasmus MC, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-2911-2140
Ivana CareyInstitute of Liver Studies, King's College Hospital, London, UK.
Jordan J FeldToronto Centre for Liver Disease, Toronto General Hospital, University of Toronto, Toronto, Canada.
Willem P BrouwerDepartment of Gastroenterology and Hepatology, Erasmus MC, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0001-8713-1481
Keyur PatelToronto Centre for Liver Disease, Toronto General Hospital, University of Toronto, Toronto, Canada.ORCID https://orcid.org/0000-0002-4677-3127
Maria ButiLiver Unit, Hospital University Valle d'Hebron and CIBEREHD del INstinuto Carlos III, Barcelona, Spain.ORCID https://orcid.org/0000-0002-0732-3078
Pieter HonkoopDepartment of Gastroenterology and Hepatology, Albert Schweitzer Hospital, Dordrecht, the Netherlands.
Douwe F PostmaDepartment of Internal Medicine and Infectious Diseases, University Medical Center Groningen, Groningen, the Netherlands.
Hans BlokzijlDepartment of Gastroenterology and Hepatology, University Medical Center Groningen, Groningen, the Netherlands.
Özgur M KocDepartment of Gastroenterology and Hepatology, Maastricht University Medical Center, Maastricht, the Netherlands.
Eva van OorschotDepartment of Gastroenterology and Hepatology, Maastricht University Medical Center, Maastricht, the Netherlands.
Kosh AgarwalInstitute of Liver Studies, King's College Hospital, London, UK.
Marc van der ValkStichting HIV Monitoring, Amsterdam, the Netherlands.
Faydra I LieveldDepartment of Gastroenterology and Hepatology, University Medical Center Utrecht, Utrecht, the Netherlands.
Mai KilanyToronto Centre for Liver Disease, Toronto General Hospital, University of Toronto, Toronto, Canada.
Matthijs KramerDepartment of Gastroenterology and Hepatology, Maastricht University Medical Center, Maastricht, the Netherlands.
Joep de BruijneDepartment of Gastroenterology and Hepatology, University Medical Center Utrecht, Utrecht, the Netherlands.
Mark A A ClaassenDepartment of Internal Medicine and Infectious Diseases, Rijnstate Hospital, Arnhem, the Netherlands.
Bettina E HansenDepartment of Epidemiology and Biostatistics, Erasmus MC, Rotterdam, the Netherlands.
Robert A de ManDepartment of Gastroenterology and Hepatology, Erasmus MC, Rotterdam, the Netherlands.
Harry L A JanssenDepartment of Gastroenterology and Hepatology, Erasmus MC, Rotterdam, the Netherlands.
R Bart TakkenbergDepartment of Gastroenterology and Hepatology, Amsterdam University Medical Center, Amsterdam, the Netherlands.
Milan J SonneveldDepartment of Gastroenterology and Hepatology, Erasmus MC, Rotterdam, the Netherlands.ORCID https://orcid.org/0000-0002-9253-563X

Funding

Gilead SciencesStichting voor Lever- en Maag-Darm Onderzoek
6 · The paper itself

Abstract

introductionMetabolic dysfunction and metabolic dysfunction-associated steatotic liver disease (MASLD) are associated with an increased risk of hepatocellular carcinoma (HCC) in patients with chronic hepatitis B (CHB). We aimed to study risk factors for HCC and to assess the performance of the PAGE-B score in this population.

methodsWe included CHB patients with ≥ 1 metabolic comorbidity from nine centres. Steatosis was diagnosed by ultrasound, CAP, or histology. Risk factors were analysed by Cox regression, and the performance of the PAGE-B score was assessed in the overall population and across relevant subgroups.

resultsWe included 1922 patients. 1730 (90.0%) were overweight, 434 (22.6%) had hypertension, 254 (13.2%) dyslipidemia, 230 (12.0%) diabetes and 732 (38.1%) MASLD. Presence of cirrhosis, older age, lower platelets and lower albumin were independent risk factors for HCC. The 5-year HCC risk was 0.1%/2.0%/12.4% patients with low/intermediate/high PAGE-B scores (p < 0.001). Consistent results were obtained in patients with MASLD (0/2.8/11.1% for low, intermediate and high PAGE-B scores (p < 0.001)). PAGE-B stratified risk in patients without cirrhosis (0% vs. 1.2% and 1.8%, p < 0.001). Among the subset of patients with cirrhosis, risks were 4.2% (low), 6.9% (intermediate) and 27.3% (high) (p < 0.001).

conclusionsCHB patients with metabolic dysfunction and/or MASLD are at significant risk of HCC. The PAGE-B score can be used to stratify HCC risk in this population, with negligible 5-year HCC incidence in those without cirrhosis and low PAGE-B scores. However, caution should be exercised in patients with cirrhosis in whom HCC risk remains significant even among those with a low PAGE-B score.

Indexed as

Carcinoma, HepatocellularFatty LiverHepatitis B, ChronicLiver NeoplasmsAdultAgedFemaleHumansLiver CirrhosisMaleMiddle AgedRisk Factorsdiabetes mellitus type 2dyslipidemiahypertensionoverweightPAGE‐B

Identifiers

PMID40922677
PMCPMC12807345

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.