Evidence map›Paper›PMID 39673688›Full record

ArticleJournal of viral hepatitis2025

Predictive Factors for HBsAg Loss in Chronic HBeAg-Negative Hepatitis B Virus Infection: Insights From a 5-Year French Cohort.

Xavier Causse, Pascal Potier, Antoine Valéry, Hélène Labadie, Gilles Macaigne, Jean-François Cadranel, Thierry Fontanges, Lina Mouna, Anne-Marie Roque-Afonso, PIBAC Study Group of Association Nationale des Hépato‐Gastroentérologues des Hôpitaux Généraux (ANGH)

Abstract read
In one paragraph

Article in Journal of viral hepatitis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. 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

10 authors.

Xavier CausseService d'Hépato-Gastroentérologie et d'Oncologie Digestive, Centre Hospitalier Universitaire d'Orléans, Orléans, France.
Pascal PotierService d'Hépato-Gastroentérologie et d'Oncologie Digestive, Centre Hospitalier Universitaire d'Orléans, Orléans, France.
Antoine ValéryDépartement d'Information Médicale, Centre Hospitalier Universitaire d'Orléans, Orléans, France.
Hélène LabadieService d'Hépato-Gastroentérologie, Centre Hospitalier de Saint Denis, Saint Denis, France.
Gilles MacaigneGroupe Hospitalier Intercommunal Le Raincy-Montfermeil, Service d'Hépato-Gastroentérologie, Le Raincy Montfermeil, France.
Jean-François CadranelGroupe Hospitalier Public du Sud de l'Oise, Service d'Hépato-Gastroentérologie, Creil, France.
Thierry FontangesPrivate Medical Practice, Maubec, France.
Lina MounaInserm U1193, Assistance Publique-Hôpitaux de Paris, Hôpital Paul Brousse, Service de Virologie, Université Paris-Saclay, Villejuif, France.
Anne-Marie Roque-AfonsoInserm U1193, Assistance Publique-Hôpitaux de Paris, Hôpital Paul Brousse, Service de Virologie, Université Paris-Saclay, Villejuif, France.ORCID 0000-0002-6612-2030
PIBAC Study Group of Association Nationale des Hépato‐Gastroentérologues des Hôpitaux Généraux (ANGH)

Funding

Association Nationale des Hépato-Gastroentérologues des hôpitaux généraux (ANGH)
6 · The paper itself

Abstract

Prognostic factors for the long-term evolution of chronic hepatitis B e antigen (HBeAg)-negative hepatitis B virus (HBV) infection may vary depending on local epidemiology. We aimed to identify these factors in France, where the epidemiology is influenced by diverse immigration. Hepatitis B surface antigen (HBsAg)-positive, HBeAg-negative adults with normal transaminase levels and viral loads < 20,000 IU/mL for 1 year, without viral co-infection or advanced liver disease, were enrolled for a 5-year follow-up. A total of 564 patients were recruited from 23 centres (54.4% women, mean age 42.3 ± 12 years, 47.7% from sub-Saharan Africa). HBV DNA was detectable but < 2000 IU/mL for most (71.3%). Genotypes E (27.8%) and A (20.0%) were predominant. The mean HBsAg titre was 3.8 ± 3.4 log IU/mL, > 1000 IU/mL in 60% of cases, and higher in genotype E (p < 0.0001). During follow-up, 18 patients received antiviral treatment, 9 for viral reactivation (0.3% per year) and 9 preemptively. HBsAg loss occurred in 39 patients (1.4% per year). These patients were older (p < 0.0001), more frequently treated for dyslipidemia, hypertension or diabetes (p < 0.05), and had lower baseline HBV DNA (p = 0.0112) and HBsAg (p < 0.0001), but similar levels of HBcrAg compared to those who did not clear HBsAg. Baseline HBsAg was the only independent predictor of HBsAg loss (p = 0.009). In this cohort, HBsAg < 153 IU/mL predicted clearance with 87% sensitivity and specificity. In conclusion, baseline HBsAg accurately predicted seroclearance at 5 years in patients with chronic HBeAg-negative infection, regardless of genotype, sex, or geographical origin, indicating that this marker is widely applicable for reducing the frequency of patient monitoring.

Indexed as

DNA, ViralHepatitis B, ChronicHepatitis B e AntigensHepatitis B Surface AntigensHepatitis B virusAdultAgedCohort StudiesFemaleFollow-Up StudiesFranceGenotypeHumansMaleMiddle AgedPrognosisDNA, ViralHepatitis B e AntigensHepatitis B Surface AntigensHBcrAgHBeAg‐negative chronic HBV infectionHBsAgHBsAg loss predictionHBV‐DNAHBV genotypeHBV reactivation

Identifiers

PMID39673688
PMCPMC11646079

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.