Evidence map›Paper›PMID 32904132›Full record

ArticleJHEP reports : innovation in hepatology2020

Hepatitis B virus preS2Δ38-55 variants: A newly identified risk factor for hepatocellular carcinoma.

Damien Cohen, Sumantra Ghosh, Yusuke Shimakawa, Njie Ramou, Pierre Simon Garcia, Anaëlle Dubois, Clément Guillot, Nora Kakwata-Nkor Deluce, Valentin Tilloy, Geoffroy Durand and 12 more

Open access · goldAbstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 3 pooled it
3.1field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 3 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  6. [Hepatocellular carcinoma (HCC)].Medecine tropicale et sante internationale · 2024
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  20. Regenerating research and life.JHEP reports : innovation in hepatology · 2020
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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

22 authors at 10 institutions in 3 countries.

Damien CohenINSERM U1052, CNRS 5286, Univ Lyon, Université Claude Bernard Lyon 1, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Sumantra GhoshINSERM U1052, CNRS 5286, Univ Lyon, Université Claude Bernard Lyon 1, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Yusuke ShimakawaUnité d'Épidémiologie des Maladies Émergentes, Institut Pasteur, Paris, France.
Njie RamouInternational Agency for Research on Cancer, Lyon, France.
Pierre Simon GarciaUniv Lyon, Université Lyon 1, CNRS, UMR5558, Laboratoire de Biométrie et Biologie Évolutive, Villeurbanne, France.
Anaëlle DuboisINSERM U1052, CNRS 5286, Univ Lyon, Université Claude Bernard Lyon 1, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Clément GuillotINSERM U1052, CNRS 5286, Univ Lyon, Université Claude Bernard Lyon 1, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Nora Kakwata-Nkor DeluceINSERM U1052, CNRS 5286, Univ Lyon, Université Claude Bernard Lyon 1, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Valentin TilloyMicrobiology Department, CHU Limoges, Genomic Platform GenoLim, UMR Inserm 1092/FR CNRS 145 GEIST, Faculté de Médecine-Université de Limoges, CHU Dupuytren, CBRS, Limoges, France.
Geoffroy DurandInternational Agency for Research on Cancer, Lyon, France.
Catherine VoegeleInternational Agency for Research on Cancer, Lyon, France.
Gibril NdowMedical Research Council Unit, The Gambia at the London School of Hygiene and Tropical Medicine, Banjul, The Gambia.
Umberto d'AlessandroMedical Research Council Unit, The Gambia at the London School of Hygiene and Tropical Medicine, Banjul, The Gambia.
Céline Brochier-ArmanetUniv Lyon, Université Lyon 1, CNRS, UMR5558, Laboratoire de Biométrie et Biologie Évolutive, Villeurbanne, France.
Sophie AlainMicrobiology Department, CHU Limoges, Genomic Platform GenoLim, UMR Inserm 1092/FR CNRS 145 GEIST, Faculté de Médecine-Université de Limoges, CHU Dupuytren, CBRS, Limoges, France.
Florence Le Calvez-KelmInternational Agency for Research on Cancer, Lyon, France.
Janet HallINSERM U1052, CNRS 5286, Univ Lyon, Université Claude Bernard Lyon 1, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Fabien ZoulimINSERM U1052, CNRS 5286, Univ Lyon, Université Claude Bernard Lyon 1, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Maimuna MendyInternational Agency for Research on Cancer, Lyon, France.
Mark ThurszDepartment of Metabolism, Digestion and Reproduction, Liver Unit, Imperial College London, London, UK.
Maud LemoineDepartment of Metabolism, Digestion and Reproduction, Liver Unit, Imperial College London, London, UK.
Isabelle CheminINSERM U1052, CNRS 5286, Univ Lyon, Université Claude Bernard Lyon 1, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Centre International de Recherche sur le Cancer · FRCentre de Recherche en Cancérologie de Lyon · FRUniversité Claude Bernard Lyon 1 · FRImperial College London · GBMRC Unit the Gambia · GMUniversité de Limoges · FRCentre National de la Recherche Scientifique · FRInserm · FRInstitut Pasteur · FRLaboratoire de Biométrie et Biologie Evolutive · FR

Funding

Medical Research Council MC_UP_A900_1119Medical Research Council MR/R011117/1World Health Organization 001
6 · The paper itself

Abstract

BACKGROUND &

aimsAlthough HBV is a major cause of death in Africa, its genetic variability has been poorly documented. This study aimed to address whether HBV genotype and surface gene variants are associated with HBV-related liver disease in The Gambia.

methodsWe conducted a case-control study nested in the Prevention of Liver Fibrosis and Cancer in Africa programme. Consecutive treatment-naive patients with chronic HBV infection and detectable viral load were recruited: 211 controls with no significant liver disease and 91 cases (56 cirrhosis and 35 HCC cases). HBV genotypes and surface gene variants were determined by Sanger sequencing or next-generation sequencing (NGS) in serum DNA. Aflatoxin B1 (AFB1)-specific codon 249

resultsIn phylogenetic analysis, 85% of individuals carried HBV genotype E, 14% genotype A, and 1% A/E recombinant viruses. Surface gene variants were more frequently observed in cases (43% and 57% in cirrhosis and HCC cases, respectively) than controls (25%;

conclusionsThis study identified a hotspot for HBV preS2 deletions as a strong independent factor for HCC in The Gambia, with HBV genotypes and AFB1 exposure contributing to the high liver cancer risk. LAY SUMMARY: Although HBV-related liver disease is highly prevalent in sub-Saharan Africa, the associated virological characteristics are poorly studied. Using clinical data from African patients chronically infected with HBV, an assessment of the virological variability (genotypes and mutations) and exposure to AFB1, a toxin often contaminating food, was carried out. Our results show that HBV genotypes, the presence of a highly prevalent mutant form of HBV, and AFB1 exposure contribute to the high liver cancer risk in this population.

Indexed as

AFB1, aflatoxin B1Aflatoxin B1AFP, alpha-fetoproteinAfricaCarcinogenesisCirrhosisER, endoplasmic reticulumGenotypeHepatitis B virusHepatocellular carcinomaLSM, liver stiffness measurementNBS1, Nijmegen breakage syndrome 1NGS, next-generation sequencingOR, odds ratioPreS deletionPROLIFICA, Prevention of Liver Fibrosis and Cancer in AfricaROC, receiver operating characteristicSSA, sub-Saharan AfricaWT, wild type

Identifiers

PMID32904132
PMCPMC7452365
OpenAlexW3042131009

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.