Evidence map›Paper›PMID 31636479›Full record

Observational studyWorld journal of gastroenterology2019

Prevalence of hepatocarcinoma-related hepatitis B virus mutants in patients in grey zone of treatment.

Ana Isabel Gil-García, Antonio Madejón, Irene Francisco-Recuero, Ana López-López, Emiliana Villafranca, Miriam Romero, Araceli García, Antonio Olveira, Rocío Mena, Juan Ramón Larrubia and 1 more

Abstract readObservational Study
In one paragraph

Observational study in World journal of gastroenterology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Indeterminate Phase/Grey Zone of Chronic Hepatitis B: Clinical Features, Outcomes and Molecular Insights.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Review
  2. Article
  3. Article
  4. State of the art treatment of hepatitis B virus hepatocellular carcinoma and the role of hepatitis B surface antigen post-liver transplantation and resection.Liver international : official journal of the International Association for the Study of the Liver · 2022
    Review
  5. Article
  6. Review
  7. Article
  8. Article
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

11 authors.

Ana Isabel Gil-GarcíaHepatology Unit, Hospital Universitario La Paz, Madrid 28046, Spain.
Antonio MadejónHepatology Unit, Hospital Universitario La Paz, Madrid 28046, Spain.
Irene Francisco-RecueroHepatology Unit, Hospital Universitario La Paz, Madrid 28046, Spain.
Ana López-LópezBiochemistry Department, Faculty of Medicine, Universidad Autónoma de Madrid, Madrid 28029, Spain.
Emiliana VillafrancaHepatology Unit, Hospital Universitario La Paz, Madrid 28046, Spain.
Miriam RomeroHepatology Unit, Hospital Universitario La Paz, Madrid 28046, Spain.
Araceli GarcíaHepatology Unit, Hospital Universitario La Paz, Madrid 28046, Spain.
Antonio OlveiraHepatology Unit, Hospital Universitario La Paz, Madrid 28046, Spain.
Rocío MenaInstituto de Genética Médica y Molecular, Hospital Universitario La Paz, Madrid 28046, Spain.
Juan Ramón LarrubiaTranslational Hepatology Unit, Hospital General Universitario de Guadalajara, Guadalajara 19002, Castilla-La Mancha, Spain.
Javier García-SamaniegoHepatology Unit, Hospital Universitario La Paz, Madrid 28046, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAntiviral treatment of patients with chronic hepatitis B (CHB) in the grey zone of treatment comands risk management in order to optimize the health outcome. In this sense, the identification of HBV mutants related with an increased risk of hepatocellular carcinoma (HCC) could be useful to identify subpopulations with potential indication of antiviral treatment.

aimTo analyze the prevalence/persistence of hepatitis B virus (HBV) preS and basal core promoter (BCP)/precore/core variants associated to HCC development in CHB patients in the grey zone.

methodsWork was designed as a longitudinal retrospective study, including 106 plasma samples from 31 patients with CHB in the grey zone of treatment: Hepatitis B e antigen negative, HBV-DNA levels between 12-20000 IU/mL, normal or discordant transaminase levels during follow up and mild/moderate necro-inflammatory activity in liver biopsy or Fibroscan (up to 9.5 kPa). Serum HBV-DNA was tested using the Abbott Real Time HBV Assay and the BCP/precore/core and the hepatitis B surface antigen (HBsAg) coding regions were analyzed in positive samples by PCR/bulk-sequencing to identify the HCC-related HBV mutants.

resultsHigh-risk HCC related mutants were detected in 24 (77%) patients: 19 (61%) in the BCP/precore/core, and 7 (23%) in the HBsAg coding region (2 preS1 and 5 preS2 deletions). The prevalence of preS deletions was genotype-dependent: 3/5 (60%) patients with preS2 deletions and 1/2 with preS1 deletions were infected with the HBV-E genotype. Since HBV-E was the most prevalent in sub-Saharan patients, a correlation between preS deletions and ethnicity was also found: 6/8 (75%) sub-Saharan

conclusionHBV genetic analysis of selected populations, like sub-Saharans infected with HBV-E/A genotypes, will allow identification of subpopulations with risk of HCC development due to accumulation of high-risk HBV variants, thus commanding their increased clinical surveillance.

Indexed as

AdultAntiviral AgentsBiopsyCarcinoma, HepatocellularDNA Mutational AnalysisDNA, ViralFemaleFollow-Up StudiesGenotypeHepatitis B, ChronicHepatitis B Surface AntigensHepatitis B virusHumansLiverLiver NeoplasmsLongitudinal StudiesAntiviral AgentsDNA, ViralHepatitis B Surface AntigensGrey zoneHepatitis B virusHepatitis B virus treatmentHepatocellular carcinomaPreS deletions

Identifiers

PMID31636479
PMCPMC6801187

What OpenQuestion holds

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LicenceCC BY-NC
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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.