Evidence map›Paper›PMID 40119917›Full record

ArticleRheumatology international2025

Altered IgG4 serum levels in VEXAS syndrome - a retrospective monocentric cohort study.

Sebastian J Saur, Benedikt Obermaier, Reinhild Klein, Matthias Hahn, Falko Fend, Sven Mattern, Joerg C Henes, Ann-Christin Pecher

Abstract read
In one paragraph

Article in Rheumatology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

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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

2 citing papers in PubMed.

  1. Review
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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

8 authors.

Sebastian J SaurDepartment of Internal Medicine II (Haematology, Oncology, Immunology and Rheumatology), University Hospital of Tuebingen, Otfried-Mueller-Strasse 10, 72076, Tuebingen, Germany.ORCID 0000-0001-7259-1207
Benedikt ObermaierDepartment of Internal Medicine II (Haematology, Oncology, Immunology and Rheumatology), University Hospital of Tuebingen, Otfried-Mueller-Strasse 10, 72076, Tuebingen, Germany. Benedikt.Obermaier@med.uni-tuebingen.de.ORCID 0009-0008-0628-870X
Reinhild KleinDepartment of Internal Medicine II (Haematology, Oncology, Immunology and Rheumatology), University Hospital of Tuebingen, Otfried-Mueller-Strasse 10, 72076, Tuebingen, Germany.ORCID 0000-0002-6111-3901
Matthias HahnDepartment of Dermatology, University Hospital of Tuebingen, Tuebingen, Germany.ORCID 0000-0001-7511-7447
Falko FendInstitute of Pathology and Neuropathology and Comprehensive Cancer Center, University Hospital of Tuebingen, Tuebingen, Germany.ORCID 0000-0002-5496-293X
Sven MatternInstitute of Pathology and Neuropathology and Comprehensive Cancer Center, University Hospital of Tuebingen, Tuebingen, Germany.ORCID 0000-0001-7362-0209
Joerg C HenesDepartment of Internal Medicine II (Haematology, Oncology, Immunology and Rheumatology), University Hospital of Tuebingen, Otfried-Mueller-Strasse 10, 72076, Tuebingen, Germany.ORCID 0000-0002-8385-6861
Ann-Christin PecherDepartment of Internal Medicine II (Haematology, Oncology, Immunology and Rheumatology), University Hospital of Tuebingen, Otfried-Mueller-Strasse 10, 72076, Tuebingen, Germany.ORCID 0000-0003-0201-0686

Funding

Deutsche Forschungsgemeinschaft Deutsche Forschungsgemeinschaft - 493665037
6 · The paper itself

Abstract

VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome is an autoinflammatory disorder characterized by somatic mutations in the UBA1 gene in hematopoietic stem cells and associated with diffuse inflammation and myelodysplastic changes amongst others. Due to unspecific symptoms the diagnosis is challenging, and there is an unmet need for clinical markers to select patients for genetic examination. Sera of 9 patients with confirmed VEXAS syndrome were analyzed for immunoglobulin (Ig)G4 levels. Disease parameters and clinical response to therapy were correlated with IgG4 levels. A histopathological examination was performed on the available samples to exclude IgG4-related autoimmune diseases. In this cohort, 44% of our patients showed markedly elevated serum IgG4 levels. We observed a general trend toward a positive correlation between IgG4 levels and inflammatory markers as well as a correlation with clinical response in one patient. Histopathological analysis showed no evidence of IgG4 related disease. IgG4 levels seem to be elevated in a relevant fraction of patients with VEXAS syndrome. In some cases, this might be misinterpreted as IgG4-related disease, a pitfall clinicians should be aware of. Furthermore, our results warrant the further evaluation of a potential correlation of IgG4 levels with disease activity and severity of inflammation. IgG4 serum levels might be useful in the evaluation of the disease course.

Indexed as

Immunoglobulin GMyelodysplastic SyndromesSkin Diseases, GeneticUbiquitin-Activating EnzymesAgedBiomarkersCohort StudiesHumansMaleMiddle AgedRetrospective StudiesBiomarkersImmunoglobulin GUBA1 protein, humanUbiquitin-Activating EnzymesAutoinflammatory diseasesImmunoglobulin G4-related diseaseMyelodysplastic syndromesUBA1 protein, humanVEXAS syndrome

Identifiers

PMID40119917
PMCPMC11929712

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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.