Evidence map›Paper›PMID 41142526›Full record

ArticleGastro hep advances2025

Long-Term Prednisone Use Increases Hepatocellular Carcinoma Risk in Autoimmune Hepatitis Cirrhosis: A Retrospective Cohort Study.

Jessica Liu, Rami Hemadeh, Abdelrahman M Attia, Pojsakorn Danpanichkul, Hasmik Adetyan, Naomy Kim, Tamar Yalda, Ju Dong Yang, Manaf Alsudaney, Walid Ayoub

Abstract read
In one paragraph

Article in Gastro hep advances, 2025. 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

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

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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

10 authors.

Jessica LiuChicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, Illinois.
Rami HemadehDepartment of Medicine, Karsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California.
Abdelrahman M AttiaDepartment of Medicine, Karsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California.
Pojsakorn DanpanichkulDepartment of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas.
Hasmik AdetyanDepartment of Medicine, Karsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California.
Naomy KimDepartment of Medicine, Karsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California.
Tamar YaldaDepartment of Medicine, Karsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California.
Ju Dong YangDepartment of Medicine, Karsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California.
Manaf AlsudaneyDepartment of Medicine, Karsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California.
Walid AyoubDepartment of Medicine, Karsh Division of Gastroenterology and Hepatology, Cedars-Sinai Medical Center, Los Angeles, California.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Autoimmune hepatitis (AIH) is an immune-mediated liver condition marked by progressive inflammation, piecemeal necrosis, and eventual cirrhosis. Prednisone has long served as the foundational AIH therapy. However, its prolonged use warrants closer evaluation regarding long-term outcomes. Among cirrhotic patients, the combination of chronic inflammatory and tumor-promoting changes may synergize to compromise immunity increasing susceptibility to hepatocellular carcinoma (HCC). In this context, adding immunosuppressive burden of corticosteroids may influence cancer risk in ways not well investigated. We investigated the effect of dose-dependent prednisone exposure on HCC risk in AIH-cirrhosis patients. Methods: We conducted a retrospective analysis of 121 adults with AIH-cirrhosis evaluated at Cedars-Sinai. Patients were categorized based on prednisone exposure: (≥7.5 mg/day for ≥6 months following cirrhosis diagnosis) exposure vs subthreshold exposure (with or without alternative therapies). The primary outcome was the HCC incidence rate and hazard ratio derived from Cox proportional hazards models. Secondary outcomes included HCC incidence using multivariable models adjusted per demographics and disease severity. Results: In unadjusted time-to-event analysis, prednisone use shortened HCC-free survival, the results indicated HCC developed in 25.4% of the prednisone group vs 9.7% of controls ( Conclusion: The study findings suggested that prolonged prednisone exposure in patients with AIH-cirrhosis independently contributes to HCC development. This association appears to be supported by mechanistic pathways, driven by prednisone's dose-dependent immunosuppressive and metabolic effects, disrupting immune surveillance, promoting hepatic fibrosis, and oncogenic pathways.

Indexed as

Autoimmune HepatitisCirrhosisHepatocellular CarcinomaPrednisone

Identifiers

PMID41142526
PMCPMC12547222

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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.