Evidence map›Paper›PMID 41589211›Full record

ArticleHepatology forum2026

Hepatic steatosis is associated with HBsAg seroclearance in patients with chronic hepatitis B virus infection but it is also associated with disease progression.

Emin Bodakci, Saba Kiremitci, Zeynep Melekoglu Ellik, Ozge Koc, Mesut Gumussoy, Volkan Yilmaz, Hale Gokcan, Atilla Halil Erhan, Sevinc Tugce Guvenir, Ramazan Erdem Er and 2 more

Abstract read
In one paragraph

Article in Hepatology forum, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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. Article
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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

12 authors.

Emin BodakciDepartment of Gastroenterology, Gaziantep City Hospital, Gaziantep, Turkiye.
Saba KiremitciDepartment of Pathology, Ankara University School of Medicine, Ankara, Turkiye.
Zeynep Melekoglu EllikDepartment of Gastroenterology, Ankara University School of Medicine, Ankara, Turkiye.
Ozge KocDepartment of Gastroenterology, Ankara University School of Medicine, Ankara, Turkiye.
Mesut GumussoyDepartment of Gastroenterology, Ankara University School of Medicine, Ankara, Turkiye.
Volkan YilmazDepartment of Gastroenterology, Ankara University School of Medicine, Ankara, Turkiye.
Hale GokcanDepartment of Gastroenterology, Ankara University School of Medicine, Ankara, Turkiye.
Atilla Halil ErhanDepartment of Biostatistics, Ankara University School of Medicine, Ankara, Turkiye.
Sevinc Tugce GuvenirDepartment of Gastroenterology, Batman Training and Research Hospital, Batman, Turkiye.
Ramazan Erdem ErDepartment of Gastroenterology, Ankara University School of Medicine, Ankara, Turkiye.
Berna SavasDepartment of Pathology, Ankara University School of Medicine, Ankara, Turkiye.
Ramazan IdilmanDepartment of Gastroenterology, Ankara University School of Medicine, Ankara, Turkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aim: The present study aimed to determine the effect of hepatic steatosis, as detected by liver biopsy, on Hepatitis B surface antigen (HbsAg) seroclearance and disease progression in patients infected with hepatitis B virus (HBV). Materials and Methods: Patients with chronic HBV infection and chronic hepatitis B (CHB) from an existing cohort of HBV-infected patients were enrolled. Results: This study included 296 patients: 186 with chronic HBV infection and 110 with CHB. Patients with chronic HBV infection were older (p=0.006), and exhibited a higher prevalence of wild-type mutants (p<0.001). At the baseline liver biopsy, 31% of the patients had hepatosteatosis. Thirty-two patients (11%) achieved HBsAg loss during the follow-up period; 72% had HBsAg seroconversion to anti-HBs. Multivariable Cox regression showed that the stage of HBV disease (chronic HBV infection vs. CHB) (Hazard ratio [HR]: 6.385, Confidence interval [CI]: 1.513-26.941, p=0.012) and grading of hepatosteatosis at baseline liver biopsy (HR: 4.699, CI: 1.662-13.286, p=0.004) were predictors of HBsAg seroclearance. Conclusion: Hepatic steatosis was associated with a functional cure for chronic HBV infection; however, it also causes disease progression in HBV-infected patients.

Indexed as

HBsAg SeroclearanceHepatitis B virushepatosteatosismetabolic dysfunction-associated steatotic liver disease

Identifiers

PMID41589211
PMCPMC12831987

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