Evidence map›Paper›PMID 42004626›Full record

ReviewJournal of translational autoimmunity2026

Autoantibodies in the follow-up of autoimmune hepatitis.

Gábor Nagy, Dóra Bencze, Sarolta Demeter, Krisztina Pénzes-Daku, Lilla Szabó, Beáta Tóth, Róza Földesi, Mária Papp, Péter Antal-Szalmás

Abstract readReview
In one paragraph

Review in Journal of translational autoimmunity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Gábor NagyDepartment of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Dóra BenczeDepartment of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Sarolta DemeterDepartment of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Krisztina Pénzes-DakuDepartment of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Lilla SzabóDepartment of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Beáta TóthDepartment of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Róza FöldesiDepartment of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Mária PappDepartment of Gastroenterology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Péter Antal-SzalmásDepartment of Laboratory Medicine, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune hepatitis (AIH) is a rare, chronic, immune mediated liver disorder with unknown origin, associated with elevation of serum transaminases and IgG, positivity of certain autoantibodies and characteristic histopathological alterations in the liver. The clinical scenario is variable, the disease can be asymptomatic for a long time, noticed accidently by liver enzyme elevation or diagnosed only when liver cirrhosis has already developed. In rare cases acute hepatitis with liver failure is the starting event. In general, immunosuppressive treatment is required to diminish the progression of liver destruction and to prevent liver transplantation. The most important autoantibodies involved in AIH diagnostics - antinuclear antibodies, smooth muscle antibodies, anti-liver kidney microsomal type 1, anti-liver cytosolic antigen 1 or anti-soluble liver antigen - can be used for definition of AIH subtypes, too. These parameters are included in current AIH diagnostic guidelines. Since the fate of the patients depends very much on the proper choice and efficacy of the applied therapy prognostic and predictive markers of disease outcome can be essential in initiating therapy, while markers of disease activity and therapy response can support follow-up. Some biochemical parameters or histopathological data can be used for these purposes, but the potential role of AIH-specific autoantibodies in these is not entirely clear. In this current review the potential use of classical and emerging autoantibodies in diagnostics, prognostics, and follow-up of AIH patients will be discussed.

Indexed as

Anti–liver kidney microsomal type 1 antibodies (anti-LKM1)Antinuclear antibodies (ANA)Anti–soluble liver antigen/liver pancreas antibodies (anti-SLA/LP)Autoimmune hepatitisAutoimmune liver diseaseSmooth muscle antibodies (SMA)

Identifiers

PMID42004626
PMCPMC13090668

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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.