Ferritin in Adult-Onset Still's Disease: Just a Useful Innocent Bystander?

Background. Adult-Onset Still's Disease (AOSD) is an immune-mediated systemic disease with quotidian-spiking fever, rash, and inflammatory arthritis. Hyperferritinemia is a prominent feature, often used for screening. Methods. The key terms "ferritin" and "hyperferritinemia"...

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Main Authors: Bella Mehta (Author), Petros Efthimiou (Author)
Format: Book
Published: Hindawi Limited, 2012-01-01T00:00:00Z.
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100 1 0 |a Bella Mehta  |e author 
700 1 0 |a Petros Efthimiou  |e author 
245 0 0 |a Ferritin in Adult-Onset Still's Disease: Just a Useful Innocent Bystander? 
260 |b Hindawi Limited,   |c 2012-01-01T00:00:00Z. 
500 |a 2090-8040 
500 |a 2042-0099 
500 |a 10.1155/2012/298405 
520 |a Background. Adult-Onset Still's Disease (AOSD) is an immune-mediated systemic disease with quotidian-spiking fever, rash, and inflammatory arthritis. Hyperferritinemia is a prominent feature, often used for screening. Methods. The key terms "ferritin" and "hyperferritinemia" were used to search PubMed and Medline and were cross-referenced with "Still's Disease." Results. Hyperferritinemia, although nonspecific, is particularly prevalent in AOSD. While most clinicians associate ferritin with iron metabolism, this is mostly true for the H isoform and not for the L isoform that tends to increase dramatically in hyperferritenemia. In these situations, hyperferritinemia is not associated with iron metabolism and may even mask an underlying iron deficiency. We review, in systematic fashion, the current basic science and clinical literature regarding the regulation of ferritin and its use in the diagnosis and management of AOSD. Conclusion. Serum hyperferritinemia in AOSD has been described for 2 decades, although its mechanism has not yet been completely elucidated. Regulation by proinflammatory cytokines such as interleukin (IL)-1b, IL-6, IL-18, MCSF, and INF-α provides a link to the disease pathogenesis and may explain rapid resolution of hyperferritinemia after targeted treatment and inhibition of key cytokines. 
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690 |a Pathology 
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786 0 |n International Journal of Inflammation, Vol 2012 (2012) 
787 0 |n http://dx.doi.org/10.1155/2012/298405 
787 0 |n https://doaj.org/toc/2090-8040 
787 0 |n https://doaj.org/toc/2042-0099 
856 4 1 |u https://doaj.org/article/f08a9793d06b4ef9a2bd5ae4152b854d  |z Connect to this object online.