AI Article Synopsis

  • Diagnosing adult-onset Still disease (AOSD) is difficult due to unclear symptoms and lack of specific blood tests, leading this study to assess the diagnostic value of clinical signs and high serum ferritin levels in patients.
  • The research involved examining patients aged over 18 with serum ferritin above 1000 ng/mL at two medical centers from 2003 to 2019, ultimately identifying 36 AOSD cases and 144 matched controls for comparison.
  • The study found that joint pain (arthralgia/arthritis) was the most reliable indicator for diagnosing AOSD, outperforming serum ferritin levels, which varied in effectiveness, supporting the idea that

Article Abstract

The diagnosis of adult-onset Still disease (AOSD) is challenging with ambiguous clinical presentation and no specific serological markers. We aim to evaluate the diagnostic utility of clinical, laboratory and serum ferritin features in established AOSD patients. We included all patients >18 years who were admitted to 2 tertiary medical centers (2003-2019) with serum ferritin above 1000 ng/mL. AOSD patients and non-AOSD controls were matched in 1:4 ratio for age and sex. The primary outcomes were sensitivity, specificity, positive/negative likelihood ratio and area under the curve (AUC) using clinical and laboratory characteristics based on the Yamaguchi classification criteria, in addition to serum ferritin. We identified 2658 patients with serum ferritin above 1000 ng/m, of whom 36 diagnosed with AOSD and 144 non-AOSD matched controls. Presence of arthralgia/arthritis showed the highest sensitivity (0.74), specificity (0.93), positive likelihood ratio (10.69), negative likelihood ratio (0.27) and AUC (0.83, 95% confidence interval 0.74-0.92) to the diagnosis of AOSD. On the other hand, serum ferritin showed variation and poorer results, depends on the chosen ferritin cutoff. Joint involvement showed the best diagnostic utility to establish the diagnosis of AOSD. Although clinicians use often elevated ferritin levels as an anchor to AOSD, the final diagnosis should be based on thorough clinical evaluation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410682PMC
http://dx.doi.org/10.1097/MD.0000000000030152DOI Listing

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