Evidence map›Paper›PMID 39247177›Full record

ArticleJHEP reports : innovation in hepatology2024

External validation of the IAIHG autoimmune hepatitis response criteria in a multicentric real-world cohort.

Lorenz Grossar, Sarah Raevens, Christophe Van Steenkiste, Isabelle Colle, Charlotte De Vloo, Hans Orlent, Jeoffrey Schouten, Marie Gallant, Annelien Van Driessche, Sander Lefere and 4 more

Abstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. JHEP reports : innovation in hepatology · 2025
    Review
  7. [Research progress on autoimmune liver disease in 2024].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2025
    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

14 authors.

Lorenz GrossarDepartment of Internal Medicine and Paediatrics, Hepatology Research Unit, Ghent University, Ghent, Belgium.
Sarah RaevensLiver Research Centre Ghent, Ghent University, Ghent University Hospital, Ghent, Belgium.
Christophe Van SteenkisteDepartment of Gastroenterology and Hepatology, AZ Maria Middelares, Ghent, Belgium.
Isabelle ColleDepartment of Gastroenterology and Hepatology, ASZ Aalst, Aalst, Belgium.
Charlotte De VlooDepartment of Gastroenterology and Hepatology, AZ Delta Roeselare, Roeselare, Belgium.
Hans OrlentDepartment of Gastroenterology and Hepatology, AZ Sint Jan Brugge, Brugge, Belgium.
Jeoffrey SchoutenDepartment of Gastroenterology and Hepatology, VITAZ, Sint-Niklaas, Belgium.
Marie GallantDepartment of Gastroenterology and Hepatology, Jan Yperman Ziekenhuis, Ieper, Belgium.
Annelien Van DriesscheDepartment of Gastroenterology and Hepatology, AZ Glorieux, Ronse, Belgium.
Sander LefereDepartment of Internal Medicine and Paediatrics, Hepatology Research Unit, Ghent University, Ghent, Belgium.
Lindsey DevisscherLiver Research Centre Ghent, Ghent University, Ghent University Hospital, Ghent, Belgium.
Anja GeertsLiver Research Centre Ghent, Ghent University, Ghent University Hospital, Ghent, Belgium.
Hans Van VlierbergheLiver Research Centre Ghent, Ghent University, Ghent University Hospital, Ghent, Belgium.
Xavier VerhelstLiver Research Centre Ghent, Ghent University, Ghent University Hospital, Ghent, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & Aims: The goal of treatment in autoimmune hepatitis (AIH) is induction of remission to prevent the development of liver fibrosis, cirrhosis, and its related complications. Various definitions of treatment response and remission have been used. The International Autoimmune Hepatitis Group (IAIHG) recently defined consensus criteria for treatment response. We aimed to validate the IAIHG response criteria in our cohort and establish correlations with survival endpoints. Methods: We performed a retrospective, multicentric cohort study in one tertiary and seven secondary care centres in Belgium. Eligible patients were at least 18 years of age at data collection and were diagnosed with AIH by a simplified IAIHG score of ≥6. Complete biochemical response (CBR) was defined according to the IAIHG consensus criteria as normalisation of transaminases and serum IgG within the first 6 months of treatment. The primary endpoint was liver-related survival - defined as freedom from liver-related death or liver transplantation. Secondary endpoints were overall mortality and transplant-free survival. Outcomes were compared between patients attaining CBR and those with insufficient response. Results: Biochemical response status could be determined in 200 patients with AIH: CBR was achieved in 128 (64.0%) individuals. Patients not achieving CBR more frequently presented with cirrhosis on initial histology (22.2% Conclusions: We externally validated the IAIHG consensus criteria for CBR and confirmed their correlation with survival endpoints in a multicentric, real-world cohort. Patients with AIH achieving CBR as an intermediate endpoint have significantly superior liver-related and overall survival. Impacts and Implications: Corticosteroids remain the cornerstone of treatment to induce remission of disease activity in autoimmune hepatitis (AIH), and the majority of patients require long-term corticosteroid treatment to achieve sustained remission. Definitions of response to treatment have varied over the years, and consistently used intermediate endpoints are needed to facilitate advancements in non-corticosteroid treatment for autoimmune hepatitis. The International Autoimmune Hepatitis Group (IAIHG) defined consensus criteria on endpoints in the treatment of AIH, for which further external validation is needed. Here, we demonstrate the usefulness of the IAIHG consensus criteria and corroborate their correlation to primary endpoints, such as liver-related survival and native liver survival in a multicentric, real-world setting. The design of future studies can rely on the IAIHG consensus criteria as intermediate endpoints.

Indexed as

autoimmune hepatitisprimary endpoints –validationsurrogate endpoints

Identifiers

PMID39247177
PMCPMC11379665

What OpenQuestion holds

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Registered trials

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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.