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Predictors of Effectiveness of Anakinra in Systemic Juvenile Idiopathic Arthritis
Benedetta Saccomanno1,2, Jessica Tibaldi1,2, Francesca Minoia1,2
1From the Università degli Studi di Genova, and the Istituto Giannina Gaslini, Genoa; Fondazione Institute for Research and Health Care (IRCCS) Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy; Instituto de Criança - Faculty of Medicine of the University of São Paulo (FMUSP), São Paulo, Brazil.
Insights
Predictors of treatment success for anakinra in children with systemic-onset juvenile idiopathic arthritis (sJIA) include shorter disease duration and higher ferritin levels. Early interleukin-1 (IL-1) inhibition may benefit specific patient profiles.
Area of Science:
- Pediatric Rheumatology
- Immunology
- Pharmacology
Background:
- Systemic-onset juvenile idiopathic arthritis (sJIA) is a severe autoimmune disease.
- Interleukin-1 (IL-1) inhibitors like anakinra offer therapeutic options for sJIA.
- Predicting response to anakinra is crucial for optimizing treatment strategies.
Purpose of the Study:
- To identify predictors of therapeutic response to anakinra in pediatric patients with sJIA.
- To delineate the clinical profile of children likely to benefit from IL-1 blockade.
Main Methods:
- Retrospective review of clinical charts for sJIA patients treated with anakinra (2004-2017).
- Analysis of demographic, clinical, and laboratory variables as potential predictors.
- Assessment of anakinra effectiveness at 1 year, defining complete clinical response (CCR).
Main Results:
- Of 62 sJIA patients, 39% achieved CCR at 1 year.
- Multivariable analysis identified shorter disease duration, lower active joint count, higher ferritin, and greater systemic activity as predictors of CCR.
- The predictive model demonstrated an area under the curve of 0.83.
Conclusions:
- Shorter disease duration, fewer active joints, higher ferritin, and more active systemic disease predict anakinra response in sJIA.
- Findings support early IL-1 inhibition for select sJIA patients.
- Further research is needed to identify biomarkers for IL-1 and IL-6 antagonist response.
Objective:
To seek predictors of therapeutic response to the interleukin (IL)-1 inhibitor anakinra in children with systemic-onset juvenile idiopathic arthritis (sJIA).
Methods:
The clinical charts of all patients with sJIA who were newly treated with anakinra at our center between 2004 and 2017 were reviewed retrospectively. Predictors included baseline demographic, clinical, and laboratory variables as well as previous or concomitant therapies. The effectiveness of anakinra was assessed at 1 year after treatment start. Complete clinical response (CCR) was defined as absence of fever, physician's global assessment ≤ 1, count of active joints ≤ 1, negative C-reactive protein, and ≥ 75% reduction of corticosteroid dose. According to the intention-to-treat principle, patients who had anakinra discontinued before 1 year for any reasons other than disease remission were classified as nonresponders. Statistics included univariate and multivariable analyses.
Results:
Of the 62 patients included in the study, 24 (39%) met the criteria for CCR at 1 year, whereas 38 (61%) did not. On multivariable analysis, independent correlations with achievement of CCR were identified for shorter disease duration, lower active joint count, higher ferritin level, and greater activity of systemic manifestations. The area under the curve of the model was 0.83.
Conclusion:
Our findings help to delineate the clinical profile of patients with sJIA who are more likely to benefit from IL-1 blockade. They also underscore the need for studies aimed at examining the therapeutic role of early IL-1 inhibition and to identify biomarkers predicting response to either IL-1 or IL-6 antagonists.
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