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CRP and sCD25 help distinguish between adult-onset Still's disease and HLH.
Beckett, Madelaine; Spaner, Caroline; Goubran, Mariam; Wade, John; Avina-Zubieta, Juan Antonio; Setiadi, Audi; Tucker, Lori; Shojania, Kam; Au, Sheila; Mattman, Andre; Lee, Agnes Y Y; Fajgenbaum, David C; Chen, Luke Y C.
Afiliação
  • Beckett M; Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Spaner C; Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Goubran M; Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
  • Wade J; Division of Rheumatology, Department of Medicine, University of British Columbia, Vancouver, Canada.
  • Avina-Zubieta JA; Division of Rheumatology, Department of Medicine, University of British Columbia, Vancouver, Canada.
  • Setiadi A; Department of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.
  • Tucker L; Division of Hematopathology, British Columbia Children's Hospital, Vancouver, Canada.
  • Shojania K; Division of Pediatric Rheumatology, Department of Pediatrics, BC Children's Hospital, University of British Columbia, Vancouver, Canada.
  • Au S; Division of Rheumatology, Department of Medicine, University of British Columbia, Vancouver, Canada.
  • Mattman A; Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada.
  • Lee AYY; Division of Hematopathology, British Columbia Children's Hospital, Vancouver, Canada.
  • Fajgenbaum DC; Department of Pathology and Laboratory Medicine, St. Paul's Hospital, Vancouver, Canada.
  • Chen LYC; Division of Hematology, Department of Medicine, University of British Columbia, Vancouver, Canada.
Eur J Haematol ; 113(5): 576-583, 2024 Nov.
Article em En | MEDLINE | ID: mdl-38984483
ABSTRACT

OBJECTIVE:

Adult-onset Still's disease (AOSD) and secondary hemophagocytic lymphohistiocytosis (sHLH) are both hyperferritinemic cytokine storm syndromes that can be difficult to distinguish from each other in hospitalized patients. The objective of this study was to compare the inflammatory markers ferritin, D-dimer, C-reactive protein (CRP), and soluble CD25 (sCD25) in patients with AOSD and sHLH. These four markers were chosen as they are widely available and represent different aspects of inflammatory diseases macrophage activation (ferritin); endothelialopathy (D-dimer); interleukin-1/interleukin-6/tumour necrosis factor elevation (CRP) and T cell activation (sCD25).

METHODS:

This was a single-center retrospective study. Patients diagnosed by the Hematology service at Vancouver General Hospital for AOSD or sHLH from 2009 to 2023 were included.

RESULTS:

There were 16 AOSD and 44 sHLH patients identified. Ferritin was lower in AOSD than HLH (median 11 360 µg/L vs. 29 020 µg/L, p = .01) while D-dimer was not significantly different (median 5310 mg/L FEU vs. 7000 mg/L FEU, p = .3). CRP was higher (median 168 mg/L vs. 71 mg/L, p <.01) and sCD25 was lower (median 2220 vs. 7280 U/mL, p = .004) in AOSD compared to HLH. The combined ROC curve using CRP >130 mg/L and sCD25< 3900 U/mL to distinguish AOSD from HLH had an area under the curve (AUC) of 0.94 (95% confidence interval 0.93-0.97) with sensitivity 91% and specificity 93%.

CONCLUSIONS:

These findings suggest that simple, widely available laboratory tests such as CRP and sCD25 can help clinicians distinguish AOSD from HLH in acutely ill adults with extreme hyperferritinemia. Larger studies examining a wider range of clinically available inflammatory biomarkers in a more diverse set of cytokine storm syndromes are warranted.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína C-Reativa / Biomarcadores / Doença de Still de Início Tardio / Linfo-Histiocitose Hemofagocítica / Subunidade alfa de Receptor de Interleucina-2 Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína C-Reativa / Biomarcadores / Doença de Still de Início Tardio / Linfo-Histiocitose Hemofagocítica / Subunidade alfa de Receptor de Interleucina-2 Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article