Evidence map›Paper›PMID 33748726›Full record

ArticleJHEP reports : innovation in hepatology2021

NAFLD and MAFLD as emerging causes of HCC: A populational study.

Shuna Myers, Isabelle Neyroud-Caspar, Laurent Spahr, Konstantinos Gkouvatsos, Evelyne Fournier, Emiliano Giostra, Giulia Magini, Jean-Louis Frossard, Marie-Eve Bascaron, Nathalie Vernaz and 3 more

Open access · goldAbstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 4 pooled it
14.2field-weighted citation impact, top 1% of its field
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

60 citing papers in PubMed, 4 syntheses or guidelines pooled it, 113 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Shuna MyersMedical Faculty, University of Geneva, Geneva, Switzerland.
Isabelle Neyroud-CasparGeneva Cancer Registry, University of Geneva, Geneva, Switzerland.
Laurent SpahrGastroenterology and Hepatology, Geneva University Hospital, Geneva, Switzerland.
Konstantinos GkouvatsosGastroenterology and Hepatology, Geneva University Hospital, Geneva, Switzerland.
Evelyne FournierGeneva Cancer Registry, University of Geneva, Geneva, Switzerland.
Emiliano GiostraGastroenterology and Hepatology, Geneva University Hospital, Geneva, Switzerland.
Giulia MaginiGastroenterology and Hepatology, Geneva University Hospital, Geneva, Switzerland.
Jean-Louis FrossardGastroenterology and Hepatology, Geneva University Hospital, Geneva, Switzerland.
Marie-Eve BascaronDivision of Palliative Medicine, Department of Rehabilitation and Geriatrics, Geneva University Hospitals, University of Geneva, Geneva, Switzerland.
Nathalie VernazMedical Directorate, Geneva University Hospital, Geneva, Switzerland.
Lucia ZampaglioneGastroenterology and Hepatology, Geneva University Hospital, Geneva, Switzerland.
Francesco NegroGastroenterology and Hepatology, Geneva University Hospital, Geneva, Switzerland.
Nicolas GoossensGastroenterology and Hepatology, Geneva University Hospital, Geneva, Switzerland.
University Hospital of Geneva · CHUniversity of Geneva · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

aimsThere are conflicting data regarding the epidemiology of hepatocellular carcinoma (HCC) arising in the context of non-alcoholic and metabolic-associated fatty liver disease (NAFLD and MAFLD). We aimed to examine the changing contribution of NAFLD and MAFLD, stratified by sex, in a well-defined geographical area and highly characterised HCC population between 1990 and 2014.

methodsWe identified all patients with HCC resident in the canton of Geneva, Switzerland, diagnosed between 1990 and 2014 from the prospective Geneva Cancer Registry and assessed aetiology-specific age-standardised incidence. NAFLD-HCC was diagnosed when other causes of liver disease were excluded in cases with type 2 diabetes, metabolic syndrome, or obesity. Criteria for MAFLD included one or more of the following criteria: overweight/obesity, presence of type 2 diabetes mellitus, or evidence of metabolic dysregulation.

resultsA total of 76/920 (8.3%) of patients were diagnosed with NAFLD-HCC in the canton of Geneva between 1990 and 2014. Between the time periods 1990-1994 and 2010-2014, there was a significant increase in HCC incidence in women (standardised incidence ratio [SIR] 1.83, 95% CI 1.08-3.13,

conclusionsIn a populational cohort spanning 25 years, the burden of NAFLD and MAFLD associated HCCs increased significantly, driving an increase in HCC incidence, particularly in women. LAY SUMMARY: Hepatocellular carcinoma (HCC) is the most common type of liver cancer, increasingly arising in patients with liver disease caused by metabolic syndrome, termed non-alcoholic fatty liver disease (NAFLD) or metabolic-associated fatty liver disease (MAFLD). We assessed all patients with HCC between 1990 and 2014 in the canton of Geneva (western Switzerland) and found an increase in all HCC cases in this timeframe, particularly in women. In addition, we found that HCC caused by NAFLD or MAFLD significantly increased over the years, particularly in women, possibly driving the increase in overall HCC cases.

Indexed as

AFP, alpha-foetoproteinALD, alcohol-related liver diseaseALT, alanine transaminaseASI, age-standardised incidenceAST, aspartate aminotransferaseFatty liverGGT, gamma-glutamyltransferaseHCC, hepatocellular carcinomaHepatocellular carcinomaHR, hazard ratioINR, international normalised ratioLiver cancerMAFLD, metabolic-associated fatty liver diseaseMELD, model for end-stage liver diseaseMetabolic syndromeNAFLD, non-alcoholic fatty liver diseaseSIR, standardised incidence ratioTACE, transarterial chemoembolisationWomen’s health

Identifiers

PMID33748726
PMCPMC7957147
OpenAlexW3122330053

What OpenQuestion holds

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LicenceCC BY
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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.