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.
References
Hayem, F. Is still’s disease an autoinflammatory syndrome? Joint Bone Spine. 76, 7–9 (2009).
Kim, Y. J., Koo, B. S., Kim, Y. G., Lee, C. K. & Yoo, B. Clinical features and prognosis in 82 patients with adult-onset still’s disease. Clin. Exp. Rheumatol. 32, 28–33 (2014).
Mitrovic, S. & Fautrel, B. Systemic juvenile idiopathic arthritis and adult-onset Still’s disease are the same disease and should now be designated by the same unique name, Still’s disease. Joint Bone Spine 92, 105872 (2025).
Fautrel, B. et al. Diagnostic value of ferritin and glycosylated ferritin in adult onset still’s disease. J. Rheumatol. 28, 322–329 (2001).
Nguyen, K. H. & Weisman, M. H. Severe sore throat as a presenting symptom of adult onset Still’s disease: A case series and review of the literature. J. Rheumatol. 24, 592–597 (1997).
Cush, J. J., Medsger, T. A., Christy, W. C., Herbert, D. C. & Cooperstein, L. A. Adult-onset Still’s disease. Clinical course and outcome. Arthritis Rheum. 30, 186–194 (1987).
Kay, J. & Upchurch, K. S. ACR/EULAR 2010 rheumatoid arthritis classification criteria. Rheumatol. (Oxford). 51 (Suppl 6), vi5–9 (2012).
Gabriel, S. E. The epidemiology of rheumatoid arthritis. Rheum. Dis. Clin. North Am. 27, 269–281 (2001).
Van Hoovels, L. et al. Multicentre study to improve clinical interpretation of rheumatoid factor and anti-citrullinated protein/peptide antibodies test results. RMD Open. 8, e002099 (2022).
Curtis, J. R. et al. A comparison of patient characteristics and outcomes in selected European and U.S. Rheumatoid arthritis registries. Semin Arthritis Rheum. 40, 2–14e1 (2010).
Courvoisier, D. S. et al. The impact of seropositivity on the effectiveness of biologic anti-rheumatic agents: Results from a collaboration of 16 registries. Rheumatology (Oxford) 60, 820–828 (2021).
Paalanen, K. et al. Does early seronegative arthritis develop into rheumatoid arthritis? A 10-year observational study. Clin. Exp. Rheumatol. 37, 37–43 (2019).
Wouters, J. M. & van de Putte, L. B. Adult-onset Still’s disease; clinical and laboratory features, treatment and progress of 45 cases. Q. J. Med. 61, 1055–1065 (1986).
Ichida, H. et al. Clinical manifestations of adult-onset Still’s disease presenting with erosive arthritis: Association with low levels of ferritin and interleukin-18. Arthritis Care Res. (Hoboken) 66, 642–646 (2014).
Neau, P.-A. et al. The spectrum of Still’s disease: A comparative analysis of phenotypic forms in a cohort of 238 patients. J. Clin. Med. 11, 6703 (2022).
Fautrel, B. et al. Proposal for a new set of classification criteria for adult-onset still disease. Medicine (Baltimore) 81, 194–200 (2002).
Yamaguchi, M. et al. Preliminary criteria for classification of adult still’s disease. J. Rheumatol. 19, 424–430 (1992).
Sokolova, M. V., Schett, G. & Steffen, U. Autoantibodies in rheumatoid arthritis: Historical background and novel findings. Clin. Rev. Allergy Immunol. 63, 138–151 (2022).
Kolarz, B., Podgorska, D. & Podgorski, R. Insights of rheumatoid arthritis biomarkers. Biomarkers 26, 185–195 (2021).
Bugatti, S. & Montecucco, C. Seronegative rheumatoid arthritis: Neglected in clinical trials, a giant in clinical practice. Joint Bone Spine 92, 105800 (2025).
Volkov, M., van Schie, K. A. & van der Woude, D. Autoantibodies and B cells: The ABC of rheumatoid arthritis pathophysiology. Immunol. Rev. 294, 148–163 (2020).
Sidiras, P. et al. Human carbamylome description identifies carbamylated α2-macroglobulin and hemopexin as two novel autoantigens in early rheumatoid arthritis. Rheumatology (Oxford) 61, 2826–2834 (2022).
Berardicurti, O. et al. Dissecting the clinical heterogeneity of adult-onset Still’s disease: Results from a multi-dimensional characterization and stratification. Rheumatology (Oxford) 60, 4844–4849 (2021).
Ruscitti, P. et al. Derivation and validation of four patient clusters in still’s disease, results from GIRRCS AOSD-study group and AIDA network still disease registry. RMD Open. 9, e003419 (2023).
Kim, H.-A., Sung, J.-M. & Suh, C.-H. Therapeutic responses and prognosis in adult-onset Still’s disease. Rheumatol. Int. 32, 1291–1298 (2012).
Lin, D. et al. Seronegative rheumatic arthritis has milder inflammation and bone erosion in an ultrasound study of disease-modifying anti-rheumatic drugs (DMARDs)-naïve Chinese cohort. Ann. Transl. Med. 10, 661 (2022).
Carbonell-Bobadilla, N. et al. Patients with seronegative rheumatoid arthritis have a different phenotype than seropositive patients: A clinical and ultrasound study. Front. Med. 9, 978351 (2022).
Kamiya, H. & Panlaqui, O. M. Systematic review and meta-analysis of the risk of rheumatoid arthritis-associated interstitial lung disease related to anti-cyclic citrullinated peptide (CCP) antibody. BMJ Open 11, e040465 (2021).
Caimmi, C., Crowson, C. S., Smith, W. M., Matteson, E. L. & Makol, A. Clinical correlates, outcomes, and predictors of inflammatory ocular disease associated with rheumatoid arthritis in the biologic era. J. Rheumatol. 45, 595–603 (2018).
Koslow, M. et al. Rheumatoid pulmonary nodules: Clinical and imaging features compared with malignancy. Eur. Radiol. 29, 1684–1692 (2019).
Barra, L. et al. Prognosis of seronegative patients in a large prospective cohort of patients with early inflammatory arthritis. J. Rheumatol. 41, 2361–2369 (2014).
Aletaha, D. et al. Rheumatoid arthritis classification criteria: an American College of Rheumatology/European League Against Rheumatism collaborative initiative. Arthritis Rheum 62, 2569–2581 (2010). (2010).
Boeters, D. M., Gaujoux-Viala, C., Constantin, A. & van der Helm-van Mil, A. H. M. The 2010 ACR/EULAR criteria are not sufficiently accurate in the early identification of autoantibody-negative rheumatoid arthritis: Results from the Leiden-EAC and ESPOIR cohorts. Semin Arthritis Rheum. 47, 170–174 (2017).
Perera, J., Delrosso, C. A., Nerviani, A. & Pitzalis, C. Clinical phenotypes, serological biomarkers, and synovial features defining seropositive and seronegative rheumatoid arthritis: A literature review. Cells 13, 743 (2024).
Nordberg, L. B. et al. Comparing the disease course of patients with seronegative and seropositive rheumatoid arthritis fulfilling the 2010 ACR/EULAR classification criteria in a treat-to-target setting: 2-year data from the ARCTIC trial. RMD Open 4, e000752 (2018).
Sokolove, J. et al. Impact of baseline anti-cyclic citrullinated peptide-2 antibody concentration on efficacy outcomes following treatment with subcutaneous abatacept or adalimumab: 2-year results from the AMPLE trial. Ann. Rheum. Dis. 75, 709–714 (2016).
Greenwood, M. et al. Methotrexate reduces withdrawal rates of TNF inhibitors due to ineffectiveness in rheumatoid arthritis but only in patients who are seropositive. Ann. Rheum. Dis. 79, 1516–1517 (2020).
Cohen, S. B. et al. A multicentre, double blind, randomised, placebo controlled trial of anakinra (Kineret), a recombinant interleukin 1 receptor antagonist, in patients with rheumatoid arthritis treated with background methotrexate. Ann. Rheum. Dis. 63, 1062–1068 (2004).
Puéchal, X. et al. Tocilizumab in refractory adult Still’s disease. Arthritis Care Res. (Hoboken) 63, 155–159 (2011).
Genovese, M. C. et al. Interleukin-6 receptor inhibition with tocilizumab reduces disease activity in rheumatoid arthritis with inadequate response to disease-modifying antirheumatic drugs: The tocilizumab in combination with traditional disease-modifying antirheumatic drug therapy study. Arthritis Rheum. 58, 2968–2980 (2008).
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
Authors and Affiliations
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
Ethics declarations
Competing interests
The authors declare no competing interests.
Additional information
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
About this article
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
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-026-40493-8