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About the complexity of adult onset Still’s disease… and advances still required for its management
© The Author(s). 2017
Received: 9 December 2016
Accepted: 9 December 2016
Published: 6 January 2017
Adult onset Still’s disease (AOSD) is a rare inflammatory disorder that remains poorly understood. Its pathophysiology is yet to be completely elucidated, but is known to consist mainly on a cytokine cascade, responsible for the systemic manifestations. AOSD diagnosis is usually difficult and delayed, with physicians having to rule out several other conditions, including cancer or infectious diseases. Prognosis is heterogeneous and difficult to establish, ranging from benign outcome to chronic destructive polyarthritis and/or life-threatening events. In addition, treatment remains to be codified, especially considering the development of new drugs. In this commentary, we attempt to elucidate the complexity of AOSD and to highlight the need of working on prognostic tools for this disorder. We also discuss the numerous advances that would be useful for patients in the daily management of this disease.
Please see related article: http://0-bmcmedicine.biomedcentral.com.brum.beds.ac.uk/articles/10.1186/s12916-016-0738-8.
More than 100 years after its first clinical description, adult onset Still’s disease (AOSD) remains challenging to diagnose and treat, and an understanding of its pathophysiology is far from being achieved . Even if the road ahead remains long and difficult, the study conducted by Ruscitti et al.  on the prognostic tools of AOSD represents a new step towards the better management of the disease. Their study, one of the largest published to date, provides confirmation of the impact of Pouchot’s ‘systemic score’ on AOSD prognosis. Indeed, these results are of significant importance considering that patient management is limited by disease complexity at the diagnosis, prognosis and therapeutic levels.
AOSD is a rare inflammatory disorder, the diagnosis of which is usually complex and delayed. Indeed, clinical presentation is heterogeneous and the main clinical features (spiking fever, joint involvement, skin rash and blood neutrophilia), as well as other minor ones (pharyngitis, lymph node or spleen enlargement, seritis, myalgia, hepatitis and abdominal pain), are unspecific . In addition, histological confirmation and relevant biomarkers are lacking in this entity (notably, determination of glycosylated ferritin level is deceiving). Therefore, diagnosis is based on criteria (Yamaguchi’s or Fautrel’s) developed for classification rather than daily practice [3, 4]. In fact, AOSD has a diagnosis of exclusion and physicians have to rule out several other striking conditions (autoimmune, infectious or malignant diseases) through a complex diagnosis procedure. Conversely, in some cases, malignancies or infections have also been reported as triggering factors for AOSD, making the understanding of clinical presentation even more complex . Disease complexity also lies in the pathophysiological mechanisms leading to a cytokine cascade (typically Th1) through an abnormal response of innate immune cells (especially macrophages) following the activation of Toll-like receptors .
Another complexity level is the highly variable prognosis, which ranges from a limited and benign outcome to chronic destructive polyarthritis and/or life-threatening involvement such as visceral complications (heart, kidney, lung or central nervous system), thrombotic microangiopathy or macrophage activation syndrome (MAS; also called reactive hemophagocytic lymphohistiocytosis) [1, 5–8]. Although exceptional, fatal events have been linked to AOSD-related complications and infections. Additionally, current treatments (i.e. NSAIDs, glucocorticoids and immunosuppressive drugs and biotherapies, in some cases) may also be deleterious, particularly in the long-term. Of note, the classification [5, 9, 10] distinguishing monocyclic, polycyclic and chronic AOSD is not useful for patient management, since it does not integrate severity and a functional and/or vital related prognosis. More precisely, it remains difficult to predict outcome at diagnosis and, consequently, drawing management guidelines presents a major challenge.
Clearly, joint involvement at diagnosis may affect functional prognosis through destructions resembling those of rheumatoid arthritis , while systemic manifestations can impair vital prognosis  (‘dichotomous view’ of AOSD ). A fever higher than 39.5 °C mainly occurs in systemic AOSD, whereas a leukocyte count higher than 30,000/mm3 and systemic inflammation markers are correlated with relapses . Increased serum ferritin levels are associated with disease activity and chronic or recurrent forms of AOSD [7, 12–14]. In 1991, from a study on 62 patients, Pouchot et al.  proposed a ‘systemic score’ reaching up to 12 points, and assigning one point to each of the following manifestations: fever, skin rash, pleuritis, pneumonia, pericarditis, liver involvement, spleen involvement, lymphadenopathy, leucocytosis > 15,000/mm3, sore throat, myalgia, and abdominal pain. This score is easy to calculate, but remains to be validated in further studies.
In their article recently published in BMC Medicine, Ruscitti et al.  report that Pouchot’s ‘systemic score’  successfully predicts a poor outcome in AOSD. More precisely, a ‘systemic score’ higher than 6 (discriminating cut-off ≥ 7) and the presence of any complication (MAS, kidney failure or myocarditis) at diagnosis are associated with mortality. Ruscitti et al.  observed MAS in 13 out of 100 patients recruited in the last 16 years, which is consistent with values in previous studies (10–15%) [8, 15]. However, death occurred in 10 patients, which is extremely high and unexepected. In AOSD, MAS is classically associated with persistent and/or refractory diseases and has been known to impair vital prognosis, but not at this level. For example, a recent Korean study identified 21 MAS among 109 AOSD patients and only two patients died , which is consistent with other published studies [8, 16]. In another recent study in Japan, the MAS-related mortality rate was approximately 20% among AOSD patients . Therefore, the high mortality rate reported by Ruscitti et al.  undoubtedly has an important weight on the results, especially for the prognostic score, but also simply reflects on the potential severity of AOSD. Finally, since MAS is in reality a life-threatening event, this should not modify our perception of these findings.
We hope that physicians will now be interested in Pouchot’s score and that further studies will simply confirm it as a prognostic tool. The discriminating cut-off predictive of death should also be evaluated and even precised. From this point of view, the study by Ruscitti et al.  represents an interesting step in the understanding of AOSD clinical presentation. Interestingly, these findings are in line with the ‘dichotomous view’ of AOSD  and could be helpful for the therapeutic decision between glucocorticoids alone or combined with immunosuppressive drugs/biologics as first-line treatment.
The final issue raised by this study concerns the methodology, whose improvement is crucial for clinical research on AOSD in the near future. In this rare inflammatory disorder, international or national (as that by Ruscitti et al. ) collaborative studies would provide the critical mass for pertinent statistical analyses and validation through evidence-based medicine.
As often observed, prognostic and therapeutic advances will probably arise from a better understanding of clinical phenotypes and pathophysiological mechanisms, and from a ‘dismemberment’ of AOSD into several entities, analogous to what ensued following the discovery of biomarkers, such as anti-neutrophil cytoplasm antibodies, on the spectrum of ‘polyarteritis nodosa’ and other vasculitides. The concept of AOSD as a disorder clinically meeting Yamaguchi’s criteria probably covers several entities with distinct pathophysiological processes but certain common inflammatory actors. Will the advances on inflammasome and cytokines help during the following years? Since AOSD is at the frontier of autoimmune and autoinflammatory disorders, the answer is ‘yes, probably’. In the end, what do the two forms of AOSD, namely systemic monophasic AOSD with high inflammation state at onset and complete recovery after several months versus chronic AOSD with systemic onset and chronic destructive sero-negative polyarthritis, have in common? The answer remains: ‘only our perplexity and ignorance…’
PG analyzed and commented recent studies on the subject. PG and ALQ equally contributed to the writing of this manuscript. Both authors read and approved the final manuscript.
ALQ is MD, PhD, and Professor of Internal Medicine at Montpellier’s University. ALQ is also the head of the department of “Internal Medicine – Multi-Organic Diseases” in Montpellier’s teaching hospital. This department is a local referral centre for rare autoimmune diseases in adult patients. PG is MD, PhD, and Associate Professor in the same university and department. ALQ and PG are both working on autoimmune and/or inflammatory diseases, in particular systemic vasculitides, systemic sclerosis and adult-onset Still’s disease.
PG is a medical expert for LFB (Laboratoire Français du Biofractionnement) and has received fees from Abbvie, Boehringrt Ingelheim France, Pfizer, and Roche in the last five years. ALQ declares that they have no competing interest.
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- Maria ATJ, Le Quellec A, Jorgensen C, Touitou I, Rivière S, Guilpain P. Adult onset Still’s disease (AOSD) in the era of biologic therapies: dichotomous view for cytokine and clinical expressions. Autoimmun Rev. 2014;13:1149–59.View ArticlePubMedGoogle Scholar
- Ruscitti P, Cipriani P, Masedu F, Iacono D, Ciccia F, Liakouli V, Guggino G, Carubbi F, Berardicurti O, Di Benedetto P, Valenti M, Triolo G, Valentini G, Giacomelli R. Adult onset Still’s disease: evaluation of prognostic tools and validation of the systemic score, by analysis of 100 cases from three centers. BMC Med. 2016;14:194.View ArticlePubMedPubMed CentralGoogle Scholar
- Yamaguchi M, Ohta A, Tsunematsu T, Kasukawa R, Mizushima Y, Kashiwagi H, et al. Preliminary criteria for classification of adult Still’s disease. J Rheumatol. 1992;19:424–30.PubMedGoogle Scholar
- Fautrel B, Zing E, Golmard J-L, Le Moel G, Bissery A, Rioux C, et al. Proposal for a new set of classification criteria for adult-onset still disease. Medicine (Baltimore). 2002;81:194–200.View ArticleGoogle Scholar
- Pouchot J, Sampalis JS, Beaudet F, Carette S, Décary F, Salusinsky-Sternbach M, et al. Adult Still’s disease: manifestations, disease course, and outcome in 62 patients. Medicine (Baltimore). 1991;70:118–36.View ArticleGoogle Scholar
- Reginato AJ, Schumacher HR, Baker DG, O’Connor CR, Ferreiros J. Adult onset Still’s disease: experience in 23 patients and literature review with emphasis on organ failure. Semin Arthritis Rheum. 1987;17:39–57.View ArticlePubMedGoogle Scholar
- Sampalis JS, Esdaile JM, Medsger TA, Partridge AJ, Yeadon C, Senécal JL, et al. A controlled study of the long-term prognosis of adult Still’s disease. Am J Med. 1995;98:384–8.View ArticlePubMedGoogle Scholar
- Arlet J-B, Le THD, Marinho A, Amoura Z, Wechsler B, Papo T, et al. Reactive haemophagocytic syndrome in adult-onset Still’s disease: a report of six patients and a review of the literature. Ann Rheum Dis. 2006;65:1596–601.View ArticlePubMedPubMed CentralGoogle Scholar
- Cush JJ, Medsger TA, Christy WC, Herbert DC, Cooperstein LA. Adult-onset Still’s disease. Clinical course and outcome. Arthritis Rheum. 1987;30:186–94.View ArticlePubMedGoogle Scholar
- Wouters JM, van de Putte LB. Adult-onset Still’s disease; clinical and laboratory features, treatment and progress of 45 cases. Q J Med. 1986;61:1055–65.PubMedGoogle Scholar
- Medsger TA, Christy WC. Carpal arthritis with ankylosis in late onset Still’s disease. Arthritis Rheum. 1976;19:232–42.View ArticlePubMedGoogle Scholar
- Kong X-D, Xu D, Zhang W, Zhao Y, Zeng X, Zhang F. Clinical features and prognosis in adult-onset Still’s disease: a study of 104 cases. Clin Rheumatol. 2010;29:1015–9.View ArticlePubMedGoogle Scholar
- Zeng T, Zou Y-Q, Wu M-F, Yang C-D. Clinical features and prognosis of adult-onset still’s disease: 61 cases from China. J Rheumatol. 2009;36:1026–31.View ArticlePubMedGoogle Scholar
- Lee S-W, Park Y-B, Song J-S, Lee S-K. The mid-range of the adjusted level of ferritin can predict the chronic course in patients with adult onset Still’s disease. J Rheumatol. 2009;36:156–62.PubMedGoogle Scholar
- Bae C-B, Jung J-Y, Kim H-A, Suh C-H. Reactive hemophagocytic syndrome in adult-onset Still disease: clinical features, predictive factors, and prognosis in 21 patients. Medicine (Baltimore). 2015;94:e451.View ArticleGoogle Scholar
- Fukaya S, Yasuda S, Hashimoto T, Oku K, Kataoka H, Horita T, et al. Clinical features of haemophagocytic syndrome in patients with systemic autoimmune diseases: analysis of 30 cases. Rheumatology. 2008;47:1686–91.View ArticlePubMedGoogle Scholar
- Kumakura S, Murakawa Y. Clinical characteristics and treatment outcomes of autoimmune-associated hemophagocytic syndrome in adults. Arthritis Rheumatol. 2014;66:2297–307.View ArticlePubMedPubMed CentralGoogle Scholar