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PredIcting SterOid DepeNdEnt LivEr InjuRy with Polyreactive Immunoglobulin G (PIONEER)

H

Hannover Medical School (MHH)

Status

Enrolling

Conditions

Autoimmune Hepatitis
Autoimmune Liver Disease

Treatments

Diagnostic Test: polyreactive immunoglobulin G

Study type

Observational

Funder types

Other

Identifiers

NCT05810480
PIONEER

Details and patient eligibility

About

The investigators identified polyreactive immunoglobulin G (pIgG) in adults (published in Hepatology: https://doi.org/10.1002/hep.32134) and children (in preparation). Quantification of these pIgG using a "home-made" ELISA facilitates the diagnosis of autoimmune hepatitis (AIH) as compared to non-AIH liver diseases and healthy controls. Positivity for pIgG was independent from ANA/SMA positivity and equally diagnostic for AIH even when conventional autoantibodies (ANA/SMA/SLA/LKM) were negative.

Additionally, the frequency of pIgG was lower than conventional autoantibodies (ANA, SMA) in vaccinia/drug associated severe liver injury in a retrospective multicenter study after Covid-19 vaccination (https://doi.org/10.1016/j.jhepr.2022.100605).

Aims of the study The study aims to evaluate the diagnostic capacity of pIgG to predict AIH in comparison to other liver diseases prospectively. To avoid diagnostic inaccuracy between AIH with long-term need for an immunosuppression and drug induced liver injury with autoimmune features, which can be indistinguishable from AIH at baseline and which has a very low relapse rate after a short steroid course, a follow-up after six months is obligatory for inclusion.

Therefore, the investigators will collect one serum sample from every patient (without immunosuppressive treatment) that presents to the respective hospital for evaluation of liver disease by liver biopsy within one year after initiation of the study and that provided written informed consent. Follow-up for evaluation of steroid dependency at six months after diagnosis is obligatory.

Enrollment

200 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnostic liver biopsy for the work-up of any liver disease
  • Informed consent
  • Definition of any liver disease according to current societal guidelines

Exclusion criteria

  • No ongoing immunosuppression at the liver biopsy or prior to the liver biopsy
  • Liver biopsies for the grading or staging of an already known liver disease (e.g. non-alcoholic fatty liver disease (NAFLD), Hepatitis B/D Virus Infections (HBV/HDV Infection), ...)

Trial design

200 participants in 2 patient groups

Autoimmune Hepatitis
Description:
This group includes patients with a diagnosis of Autoimmune Hepatitis according to the simplified diagnostic criteria by Hennes et al. made by the local treating physician. The diagnosis of autoimmune hepatitis additionally requires steroid dependency \> six months for this study to discriminate Autoimmune Hepatitis from autoimmune like drug-induced liver injury (DILI) which are hard to discriminate at diagnosis and with the latter often being treating with a short course of corticosteroids less than six months. One serum sample will be stored for anonymized evaluation of serum autoantibodies
Treatment:
Diagnostic Test: polyreactive immunoglobulin G
non-autoimmune hepatitis liver disease
Description:
This group includes patients with a diagnosis of any non-viral liver disease that is not autoimmune hepatitis and whose diagnosis necessitated a diagnostic liver biopsy in the work-up of the liver disease for local care. One serum sample will be stored for anonymized evaluation of serum autoantibodies
Treatment:
Diagnostic Test: polyreactive immunoglobulin G

Trial contacts and locations

8

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Central trial contact

Richard Taubert, Dr.; Bastian Engel, Dr.

Data sourced from clinicaltrials.gov

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