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Clustering reveals diagnostic overlap between Still’s disease and a hyperinflammatory subset of seronegative rheumatoid arthritis
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  • Published: 24 February 2026

Clustering reveals diagnostic overlap between Still’s disease and a hyperinflammatory subset of seronegative rheumatoid arthritis

  • Alexandre Mercier-Guery1,2,3 na1,
  • Thomas El-Jammal4,5 na1,
  • Nour El-Nayef1,3,6,
  • Emmanuel Massy1,6,
  • Nicolas Fournier4,5,
  • Pascal Sève4,5,
  • Cyrille Confavreux1,6,
  • Yvan Jamilloux4,5 na1 &
  • …
  • Fabienne Coury1,2,3 na1 

Scientific Reports , Article number:  (2026) Cite this article

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Diseases
  • Immunology
  • Medical research
  • Rheumatology

Abstract

Still’s disease (SD) and rheumatoid arthritis (RA), particularly seronegative RA, may overlap clinically and biologically, complicating diagnosis. We explored data-driven overlaps between SD, seronegative RA, and seropositive RA using unsupervised clustering. We retrospectively included 312 adults: 98 SD from the multicentric AURAL Still cohort and 214 RA (93 seropositive, 121 seronegative). Baseline clinical and laboratory data were analysed using factor analysis of mixed data followed by k-means clustering. SD patients were younger than RA patients and more frequently presented with fever and systemic features. Inflammatory markers (notably CRP and ferritin) were higher in SD than in both RA subsets. Three clusters were identified: Cluster 1 (n = 196) mainly comprised seropositive (45%) and seronegative RA (50%), with mild systemic inflammation and symmetrical polyarthritis; Cluster 2 (n = 73) was predominantly SD (92%), with systemic features, high inflammation and polyarthritis, and more frequent spontaneous remission without treatment; Cluster 3 (n = 43) mixed SD (49%) and seronegative RA (42%), characterised by moderate inflammation and asymmetrical oligoarthritis with low autoantibody rates. Most seronegative RA clustered with classical RA, but ~ 20% overlapped with SD-like phenotypes, suggesting a hyper-inflammatory subset which could be conceptualized as Systemic Inflammatory RA (SIRA). This proposal is hypothesis-generating and warrants prospective validation.

Data availability

The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.

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Acknowledgements

The authors thank all participating patients. We are grateful to the contributors to the participating registries for case identification and data curation, including Leopold Adelaide, Orlane Chol, Charline Estublier, Marine Gaude, Mathieu Gerfaud-Valentin, Clément Javaux, Jean-Paul Larbre, Pierre-Antoine Neau, and Muriel Piperno.

Author information

Author notes
  1. Alexandre Mercier-Guery, Thomas El-Jammal, Yvan Jamilloux and Fabienne Coury contributed equally to this work.

Authors and Affiliations

  1. University of Lyon, University Lyon 1, Lyon, 69100, France

    Alexandre Mercier-Guery, Nour El-Nayef, Emmanuel Massy, Cyrille Confavreux & Fabienne Coury

  2. Department of Rheumatology, Edouard Herriot Hospital, Hospices Civils de Lyon, Lyon, 69003, France

    Alexandre Mercier-Guery & Fabienne Coury

  3. INSERM UMR 1033, Lyon, 69100, France

    Alexandre Mercier-Guery, Nour El-Nayef & Fabienne Coury

  4. Internal medicine, National Reference Center for AutoInflammatory Diseases (CEREMAIA), University Hospital Croix-Rousse, Hospices Civils de Lyon, Lyon, 69004, France

    Thomas El-Jammal, Nicolas Fournier, Pascal Sève & Yvan Jamilloux

  5. Tissular Biology Laboratory, Institute of Protein Biology and Chemistry, UMR CNRS 5305 Therapeutic Engineering, Lyon, 69007, France

    Thomas El-Jammal, Nicolas Fournier, Pascal Sève & Yvan Jamilloux

  6. Department of Rheumatology, Lyon Sud Hospital, Hospices Civils de Lyon, Pierre- Bénite, F-69495, France

    Nour El-Nayef, Emmanuel Massy & Cyrille Confavreux

Authors
  1. Alexandre Mercier-Guery
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Contributions

Conceptualization: AMG, TE, YJ, FC. Methodology: AMG, TE, YJ, FC. Data acquisition/Investigation: AMG, NE, NF. Data curation: AMG, TE, NE. Formal analysis: AMG, TE. Interpretation of data: AMG, TE, PS, YJ, FC. Writing – original draft: AMG, NE. Writing – review & editing: EM, PS, NF, CC, YJ, FC. Supervision: YJ, FC. Project administration: AMG, FC. All authors approved the submitted version and agree to be personally accountable for their own contributions, and to ensure that questions related to the accuracy or integrity of any part of the work are appropriately investigated, resolved, and documented in the literature.

Corresponding author

Correspondence to Alexandre Mercier-Guery.

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Cite this article

Mercier-Guery, A., El-Jammal, T., El-Nayef, N. et al. Clustering reveals diagnostic overlap between Still’s disease and a hyperinflammatory subset of seronegative rheumatoid arthritis. Sci Rep (2026). https://doi.org/10.1038/s41598-026-40493-8

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  • Received: 28 November 2025

  • Accepted: 13 February 2026

  • Published: 24 February 2026

  • DOI: https://doi.org/10.1038/s41598-026-40493-8

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