Actively Recruiting

All Genders
NCT05810480

PredIcting SterOid DepeNdEnt LivEr InjuRy with Polyreactive Immunoglobulin G

Led by Hannover Medical School · Updated on 2024-10-16

200

Participants Needed

8

Research Sites

186 weeks

Total Duration

On this page

AI-Summary

What this Trial Is 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.

CONDITIONS

Official Title

PredIcting SterOid DepeNdEnt LivEr InjuRy with Polyreactive Immunoglobulin G

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnostic liver biopsy for the work-up of any liver disease
  • Informed consent
  • Definition of any liver disease according to current societal guidelines
Not Eligible

You will not qualify if you...

  • Ongoing immunosuppression at or prior to the liver biopsy
  • Liver biopsies done only for grading or staging of a known liver disease such as non-alcoholic fatty liver disease or Hepatitis B/D virus infections

AI-Screening

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Trial Site Locations

Total: 8 locations

1

University Medical Centre Aachen

Aachen, Germany, 52074

Actively Recruiting

2

University Hospital Bonn

Bonn, Germany

Actively Recruiting

3

University Medical Center Hamburg-Eppendorf

Hamburg, Germany, 20251

Actively Recruiting

4

Hannover Medical School

Hanover, Germany, 30625

Actively Recruiting

5

University Medical Center Heidelberg

Heidelberg, Germany, 69120

Actively Recruiting

6

University Hospital Schleswig-Holstein, Location Lübeck

Lübeck, Germany, 23562

Actively Recruiting

7

University Hospital Magdeburg

Magdeburg, Germany, 39120

Actively Recruiting

8

Rostock University Medical Centre

Rostock, Germany, 18057

Actively Recruiting

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Research Team

B

Bastian Engel, Dr.

CONTACT

R

Richard Taubert, Dr.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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