Evidence map›Paper›PMID 41098242›Full record

ArticleJHEP reports : innovation in hepatology2025

Isolated IgG elevation in patients with persistently normal transaminases does not affect the outcome of autoimmune hepatitis.

Álvaro Díaz-González, Ida Schregel, Lorena Carballo, Carmen Álvarez-Navascués, Enrique Frisancho-Morales, Mireia Miquel, Montserrat García Retortillo, Judith Gómez, Diana Horta, Beatriz Mateos and 23 more

Abstract read
In one paragraph

Article in JHEP reports : innovation in hepatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Reply to 'Biopsy Before Autoimmune Hepatitis Withdrawal: The Estimand Matters'.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Article
  3. Article
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

33 authors.

Álvaro Díaz-GonzálezGastroenterology and Hepatology Department, Clinical and Translational Research in Digestive Diseases Group, Valdecilla Research Institute (IDIVAL), Marqués de Valdecilla University Hospital, Santander, Spain.
Ida SchregelDepartment of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Lorena CarballoDigestive Diseases Department, Hospital Universitario Central de Asturias, Oviedo, Spain.
Carmen Álvarez-NavascuésDigestive Diseases Department, Hospital Universitario Central de Asturias, Oviedo, Spain.
Enrique Frisancho-MoralesLiver Unit, Digestive Diseases Department, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí I3PT, Universitat Autònoma de Barcelona, Sabadell, Spain.
Mireia MiquelLiver Unit, Digestive Diseases Department, Parc Taulí Hospital Universitari, Institut d'Investigació i Innovació Parc Taulí I3PT, Universitat Autònoma de Barcelona, Sabadell, Spain.
Montserrat García RetortilloDigestive Diseases Department, Hospital del Mar-Parc de Salut Mar, Barcelona, Spain.
Judith GómezDigestive Diseases Department, Hospital Universitario de Burgos, Burgos, Spain.
Diana HortaDigestive Diseases Department, Hospital Universitari Mutua de Terrassa, Terrassa, Spain.
Beatriz MateosDigestive Diseases Department, Hospital Universitario Ramón y Cajal, CIBERehd, IRYCIS, Madrid, Spain.
Bastian EngelEuropean Reference Network on Hepatological Diseases (ERN RARE-LIVER).
Felix VolmerEuropean Reference Network on Hepatological Diseases (ERN RARE-LIVER).
María Del BarrioGastroenterology and Hepatology Department, Clinical and Translational Research in Digestive Diseases Group, Valdecilla Research Institute (IDIVAL), Marqués de Valdecilla University Hospital, Santander, Spain.
Sergio Rodríguez-TajesLiver Unit, Hospital Clínic Barcelona, Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi i Sunyer (FRCB-IDIBAPS), Universitat de Barcelona, Centro de investigación Biomédica en Red Enfermedades Hepáticas y Digestivas (CIBEREHD), Barcelona, Spain.
Ignasi OlivasLiver Unit, Hospital Clínic Barcelona, Fundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi i Sunyer (FRCB-IDIBAPS), Universitat de Barcelona, Centro de investigación Biomédica en Red Enfermedades Hepáticas y Digestivas (CIBEREHD), Barcelona, Spain.
Johannes HartlDepartment of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Carla Amaral GonzálezDigestive Diseases Department, Hospital Universitario de Canarias, La Laguna, Spain.
Manuel Hernández-GuerraDigestive Diseases Department, Hospital Universitario de Canarias, La Laguna, Spain.
Inmaculada CastelloDigestive Diseases Department, Hospital General Universitari de Valencia, Valencia, Spain.
Indhira Pérez-MedranoDepartment of Hepatology, Complexo Hospitalario Universitario de Pontevedra, Instituto de Investigación Sanitaria Galicia Sur (IISGS) Pontevedra, Spain.
Jesús M González-SantiagoDigestive Diseases Department, Complejo Asistencial Universitario de Salamanca, Laboratorio de Hepatología Experimental y Vectorización de Fármacos (HEVEPHARM), CIBERehd, IBSAL, Salamanca, Spain.
Ana ArencibíaDigestive Diseases Department, Hospital Universitario Nuestra Señora de la Candelaria, Santa Cruz de Tenerife, Spain.
Alberto GómezDepartment of Hepatology and Liver Transplantation, Hospital Universitario Reina Sofía, IMIBIC, CIBERehd, Córdoba, Spain.
Manuel Rodríguez-PerálvarezDepartment of Hepatology and Liver Transplantation, Hospital Universitario Reina Sofía, IMIBIC, CIBERehd, Córdoba, Spain.
Javier CrespoGastroenterology and Hepatology Department, Clinical and Translational Research in Digestive Diseases Group, Valdecilla Research Institute (IDIVAL), Marqués de Valdecilla University Hospital, Santander, Spain.
Margarita SalaLiver Unit, Digestive Diseases Department, Hospital Universitari Doctor Josep Trueta, IDIBGI (Institut d'Investigació Biomèdica de Girona), CIBEREHD, Girona, Spain.
Magdalena SalcedoDigestive Diseases Department, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Ana Barreira-DíazEuropean Reference Network on Hepatological Diseases (ERN RARE-LIVER).
Mar Riveiro-BarcielaEuropean Reference Network on Hepatological Diseases (ERN RARE-LIVER).
Richard TaubertEuropean Reference Network on Hepatological Diseases (ERN RARE-LIVER).
Christoph SchrammDepartment of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
María-Carlota LondoñoEuropean Reference Network on Hepatological Diseases (ERN RARE-LIVER).
ColHai Registry

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & Aims: The goal of treatment for autoimmune hepatitis is to achieve a complete biochemical response, defined as normalization of transaminases and immunoglobulin G (IgG) levels. Recent data suggest that IgG normalization does not significantly affect survival. We evaluated the impact of persistently elevated IgG levels (IgGe) and IgG flares (IgGf) on fibrosis progression and cirrhosis development. Methods: This retrospective multicenter cohort study included 493 patients with autoimmune hepatitis and persistently normal transaminase levels during follow-up. The inverse probability of treatment weighting (IPTW) propensity score method was used to balance the cohorts. Results: Three hundred forty-nine (70.8%) patients had persistently normal IgG (IgGn) levels, 89 (18.1%) had IgGe, and 55 (11.1%) had IgGf during follow-up. After a median follow-up of 6.2 years (IQR 4.1-10.1 years) with normal transaminase levels, median liver stiffness measurement (LSM) values remained stable, with no significant differences between groups. During the follow-up, 24 patients developed cirrhosis. Predictive factors for cirrhosis were age (hazard ratio [HR] 1.10, Conclusions: Persistent or temporary serum IgG elevation in patients with normal transaminase levels did not significantly affect autoimmune hepatitis disease progression, thus challenging the current definition of complete biochemical response. Impact and implications: The body of evidence showing a lesser impact of immunoglobulin G (IgG)values on outcomes in patients with autoimmune hepatitis (AIH) is growing. However, there is still a lack of robust information on the long-term outcomes, especially in patients who achieve persistent transaminase normalization. Persistently elevated IgG or IgG flares in patients with persistently normal transaminases do not seem to affect outcomes in patients with AIH. These results challenge the current definition of complete biochemical response in patients with AIH. Transaminase level normalization appeared to be the best treatment endpoint.

Indexed as

Autoimmune hepatitisComplete biochemical responseImmunoglobulin G

Identifiers

PMID41098242
PMCPMC12519241

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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.