Volume 58, Issue 12 pp. 3924-3931
Childhood Arthritis

S100A12 is a novel molecular marker differentiating systemic-onset juvenile idiopathic arthritis from other causes of fever of unknown origin

Helmut Wittkowski

Helmut Wittkowski

University Hospital Muenster, and University of Muenster, Muenster, Germany

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Michael Frosch

Michael Frosch

University Hospital Muenster, and University of Muenster, Muenster, Germany

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Nico Wulffraat

Nico Wulffraat

Wilhelmina Children's Hospital, and University Medical Centre, Utrecht, The Netherlands

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Raphaela Goldbach-Mansky

Raphaela Goldbach-Mansky

National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland

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Tilmann Kallinich

Tilmann Kallinich

Charité Children's Hospital, Berlin, Germany

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Jasmin Kuemmerle-Deschner

Jasmin Kuemmerle-Deschner

University Children's Hospital, and University of Tuebingen, Tuebingen, Germany

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Michael C. Frühwald

Michael C. Frühwald

University Hospital Muenster, and University of Muenster, Muenster, Germany

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Sandra Dassmann

Sandra Dassmann

University Hospital Muenster, and University of Muenster, Muenster, Germany

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Tuyet-Hang Pham

Tuyet-Hang Pham

National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland

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Johannes Roth

Corresponding Author

Johannes Roth

University Hospital Muenster, and University of Muenster, Muenster, Germany

Dr. Roth has applied for a patent for a method of diagnosing inflammatory diseases using calgranulin C (US patent application 10/504299).

Department of Pediatrics, University of Muenster, Albert-Schweitzer-Strasse 33, D-48149 Muenster, GermanySearch for more papers by this author
Dirk Foell

Dirk Foell

University Hospital Muenster, and University of Muenster, Muenster, Germany

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First published: 26 November 2008
Citations: 171

Abstract

Objective

Fever of unknown origin (FUO) in children presents a diagnostic challenge. The differential diagnosis includes systemic-onset juvenile idiopathic arthritis (JIA), an autoinflammatory syndrome associated with activation of phagocytic cells that, at presentation, is difficult to differentiate from severe systemic infections. The aim of this study was to investigate whether serum concentrations of the phagocytic proinflammatory protein S100A12 may help in deciding whether to treat patients with FUO with antibiotics or immunosuppressive agents.

Methods

Serum samples were obtained from 45 healthy control subjects and from 240 patients (60 with systemic-onset JIA, 17 with familial Mediterranean fever [FMF], 18 with neonatal-onset multisystem inflammatory disease [NOMID], 17 with Muckle-Wells syndrome [MWS], 40 with acute lymphoblastic leukemia [ALL], 5 with acute myeloblastic leukemia [AML], and 83 with systemic infections). All samples were collected at the time of presentation, before the initiation of any treatment, and concentrations of S100A12 were determined by enzyme-linked immunosorbent assay.

Results

The mean ± 95% confidence interval serum levels of S100A12 were as follows: in patients with JIA, 7,190 ± 2,690 ng/ml; in patients with FMF, 6,720 ± 4,960 ng/ml; in patients with NOMID, 720 ± 450 ng/ml; in patients with MWS, 150 ± 60 ng/ml; in patients with infections, 470 ± 160 ng/ml; in patients with ALL, 130 ± 80 ng/ml; in patients with AML, 45 ± 60 ng/ml; in healthy control subjects, 50 ± 10 ng/ml. The sensitivity and specificity of S100A12 to distinguish between systemic-onset JIA and infections were 66% and 94%, respectively.

Conclusion

S100A12, a marker of granulocyte activation, is highly overexpressed in patients with systemic-onset JIA or FMF, which may point to as-yet unknown common inflammatory mechanisms in these diseases. The measurement of S100A12 serum levels may provide a valuable diagnostic tool in the evaluation of FUO.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.

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