Pathogenesis, disease course, and prognosis of adult-onset Still's disease: an update and review / 中华医学杂志(英文版)
Chinese Medical Journal
;
(24): 2856-2864, 2019.
Artigo
em Inglês
| WPRIM
| ID: wpr-781733
ABSTRACT
OBJECTIVE@#Adult-onset Still's disease (AOSD) is a rare but clinically well-known polygenic systemic autoinflammatory disease. In this review, we aim to present frontiers in the pathogenesis, clinical features, diagnosis, biomarkers, disease course, prognosis, and treatment in AOSD.@*DATA SOURCES@#We retrieved information from the PubMed database up to July 2019, using various search terms and relevant words, including AOSD and Still's disease.@*STUDY SELECTION@#We included data from peer-reviewed journals. Both basic and clinical studies were selected.@*RESULTS@#Pathogenesis of AOSD involves genetic background, infectious triggers, and immunopathogenesis, mainly the activation of macrophages and neutrophils followed by a cytokine storm. Diagnosis and prognosis evaluation of AOSD is still challenging; therefore, there is an urgent need to identify better biomarkers. Biologic agents, including interleukin (IL)-1β, IL-6, and tumor necrosis factor-α antagonists in the treatment of AOSD, have good prospect.@*CONCLUSION@#This review highlights the advances in pathogenesis, potential biomarkers, disease course, and treatment in AOSD.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Tipo de estudo:
Estudo de etiologia
/
Estudo prognóstico
Idioma:
Inglês
Revista:
Chinese Medical Journal
Ano de publicação:
2019
Tipo de documento:
Artigo
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