Evidence map›Paper›PMID 41689654›Full record

ReviewRheumatology international2026

Azathioprine as maintenance therapy for IgG4-related diseases: a retrospective case series and case-based review of the literature.

Myriam Reisch, Walter Johann Spindelböck, Isabel Hodl, Daniel Pietsch, Florian Rainer, David Kickinger, Anamarija Sutic, Jens Thiel, Martin Stradner

Abstract readReview
In one paragraph

Review in Rheumatology international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Myriam ReischDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria. Myriam.Reisch@medunigraz.at.ORCID http://orcid.org/0009-0003-3578-8205
Walter Johann SpindelböckDepartment of Gastroenterology and Hepatology, Medical University of Graz, Graz, Austria.ORCID http://orcid.org/0000-0002-6301-4675
Isabel HodlDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.ORCID http://orcid.org/0000-0003-4044-0046
Daniel PietschDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.
Florian RainerDepartment of Gastroenterology and Hepatology, Medical University of Graz, Graz, Austria.ORCID http://orcid.org/0000-0002-8339-8821
David KickingerDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.ORCID http://orcid.org/0009-0006-5186-0483
Anamarija SuticDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.
Jens ThielDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.ORCID http://orcid.org/0000-0001-7582-1514
Martin StradnerDepartment of Rheumatology and Immunology, Medical University of Graz, Graz, Austria.ORCID http://orcid.org/0000-0002-7884-6626

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IgG4-related disease (IgG4-RD) is a rare fibro-inflammatory disorder characterized by progressive fibrosis involving multiple organs and tissues. Clinical manifestations are highly variable, reflecting the organs affected. Oral glucocorticoids (GC) are established as first-line therapy; however, relapse occurs in 15–60% of patients. To reduce relapse risk and GC-related adverse effects, GC-sparing strategies using disease-modifying antirheumatic drugs (DMARDs) may be considered. This study aims to evaluate the efficacy and safety of azathioprine in the management of IgG4-RD and provides an overview of the current literature. This retrospective case series assesses disease activity under azathioprine therapy in patients with IgG4-RD treated at the Medical University of Graz between 2006 and 2024. Patients with a confirmed IgG4-RD diagnosis according to the 2019 ACR/EULAR criteria who received azathioprine following initial GC therapy were included. Ten male patients (mean age at disease onset: 59.4 years) with a mean follow-up of 75.2 months were analyzed. All patients fulfilled the 2019 ACR/EULAR classification criteria. Indications for initiating azathioprine included disease relapse on GC (n = 3), GC-related adverse effects (n = 3), and the intention to reduce GC exposure (n = 7). During azathioprine therapy, three patients (30%) experienced a total of five relapses. Seven patients receiving azathioprine remained in remission throughout the observation period. Adverse events included infections (n = 2), hematologic abnormalities (n = 4), and elevated liver enzymes (n = 1). At last follow-up, five patients (50%) remained on azathioprine, two (20%) had switched to rituximab, one of whom was in remission and off therapy, and three patients (30%) were no longer receiving immunosuppressive treatment (two due to hematologic abnormalities, one by patient request), with no further therapy initiated. Azathioprine represents an appropriate maintenance therapy for IgG4-RD. In cases with relapse under azathioprine, alternative DMARDs, such as CD19- or CD20-targeted therapies, may be more effective.

Indexed as

Antirheumatic AgentsAzathioprineImmunoglobulin G4-Related DiseaseImmunosuppressive AgentsAgedGlucocorticoidsHumansMaleMiddle AgedRecurrenceRetrospective StudiesTreatment OutcomeAntirheumatic AgentsAzathioprineGlucocorticoidsImmunosuppressive AgentsAntirheumatic agentsAzathioprineImmunoglobulin G4-related diseaseRecurrenceRetrospective studies

Identifiers

PMID41689654
PMCPMC12906543

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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.