Evidence map›Paper›PMID 40980159›Full record

ArticleJHEP reports : innovation in hepatology2025

Autoantibodies are associated with worse outcomes in MASLD.

Anna Soria, Alba Díaz, Paula Iruzubieta, Rosa Martín-Mateos, M Teresa Salcedo-Allende, Alba Jiménez-Masip, Carla Fuster-Anglada, María Teresa Arias-Loste, Cristian Perna, Cautar El Maimouni and 24 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. Article
  3. Association Between Khat (Biomarker insights · 2026
    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

34 authors.

Anna SoriaLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Alba DíazFundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi i Sunyer (FRCB-IDIBAPS), Barcelona, Spain.
Paula IruzubietaGastroenterology and Hepatology Department, Marqués de Valdecilla University Hospital, Clinical and Translational Research in Digestive Diseases, Valdecilla Research Institute (IDIVAL), Santander, Spain.
Rosa Martín-MateosCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CiberEHD), Barcelona, Spain.
M Teresa Salcedo-AllendeLiver Unit, Vall d'Hebron Hospital Universitari, Vall d'Hebron Institut of Research (VHIR), Vall d'Hebron Barcelona Hospital Campus, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
Alba Jiménez-MasipLiver Unit, Vall d'Hebron Hospital Universitari, Vall d'Hebron Institut of Research (VHIR), Vall d'Hebron Barcelona Hospital Campus, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
Carla Fuster-AngladaFundació de Recerca Clínic Barcelona-Institut d'Investigacions Biomèdiques August Pi i Sunyer (FRCB-IDIBAPS), Barcelona, Spain.
María Teresa Arias-LosteGastroenterology and Hepatology Department, Marqués de Valdecilla University Hospital, Clinical and Translational Research in Digestive Diseases, Valdecilla Research Institute (IDIVAL), Santander, Spain.
Cristian PernaServicio de Anatomía Patológica, Hospital Universitario Ramón y Cajal, IRYCIS, Universidad de Alcalá, Madrid, Spain.
Cautar El MaimouniLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Juan Manuel PericasCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CiberEHD), Barcelona, Spain.
Ana Ferrer-GómezServicio de Anatomía Patológica, Hospital Universitario Ramón y Cajal, IRYCIS, Universidad de Alcalá, Madrid, Spain.
Carolina Jiménez GonzálezGastroenterology and Hepatology Department, Marqués de Valdecilla University Hospital, Clinical and Translational Research in Digestive Diseases, Valdecilla Research Institute (IDIVAL), Santander, Spain.
Sergio Muñoz-MartínezCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CiberEHD), Barcelona, Spain.
Marlene PadillaLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Javier CrespoGastroenterology and Hepatology Department, Marqués de Valdecilla University Hospital, Clinical and Translational Research in Digestive Diseases, Valdecilla Research Institute (IDIVAL), Santander, Spain.
Zyanya CalixtoServicio de Anatomía Patológica, Hospital Universitari Vall d'Hebron de Barcelona, Universidad Autònoma de Barcelona, Barcelona, Spain.
Clara SabioteLiver Unit, Vall d'Hebron Hospital Universitari, Vall d'Hebron Institut of Research (VHIR), Vall d'Hebron Barcelona Hospital Campus, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.
Agustín AlbillosCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CiberEHD), Barcelona, Spain.
Marta CerveraLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Ignasi OlivasLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Pinelopi ArvanitiLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Helena Hernández-ÉvoleLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Natalia Jiménez-EsquivelLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Jordi Gratacós-GinèsLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Adrià JuanolaLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Elisa PoseLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Mar CollFaculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Ruth NadalLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Martina Pérez-GuaschLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Núria FabrellasFaculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Pere GinèsLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
María-Carlota LondoñoLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.
Isabel GrauperaLiver Unit Hospital Clínic, Faculty of Medicine and Health Sciences, Universitat de Barcelona (UB), Barcelona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background & Aims: Metabolic dysfunction-associated steatotic liver disease (MASLD) is a leading cause of chronic liver disease worldwide. Autoantibodies (Ab), such as antinuclear antibodies (ANA) and anti-smooth muscle antibodies (ASMA), are frequently detected in MASLD, but their role in disease progression remains controversial. This study aimed to evaluate the prevalence of positive Ab and the histological features of autoimmune hepatitis (AIH) in MASLD and their association with liver-related outcomes. Methods: We conducted a multicenter, retrospective, longitudinal study of patients with biopsy-proven MASLD from the HEPAmet Registry. Data on ANA (≥1/80), ASMA (≥1/40), and AIH histological features (portal inflammation, interface hepatitis, and plasma cell infiltration) were analyzed for their association with compensated advanced chronic liver disease (cACLD), liver decompensation, and death. Results: Of the 460 patients (49% women, median age 58 years, median BMI 33 kg/m Conclusions: ANA and ASMA are commonly found in patients with MASLD and are associated with poorer liver-related outcomes and reduced survival, whereas isolated histological autoimmune features provide no additional prognostic value. Impact and implications: Metabolic dysfunction-associated steatotic liver disease (MASLD) can coexist with other liver diseases, including autoimmune hepatitis. The role of autoantibodies and histological autoimmune features in MASLD progression remains controversial. Understanding the relationship between autoimmune characteristics and disease progression in MASLD may help physicians identify high-risk populations, enhance risk stratification, and personalize disease treatment.

Indexed as

AutoantibodiesAutoimmune hepatitisCirrhosisDecompensationMetabolic dysfunction-associated steatotic liver diseaseSurvival

Identifiers

PMID40980159
PMCPMC12446532

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

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 Socratic graph.