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90K immunostimulatory glycoprotein in children with juvenile idiopathic arthritis
Cristina Cecamore1, Manuela Marsili1, Roberta Salvatore1
1a Department of Pediatrics , University of Chieti , Chieti , Italy.
Insights
Levels of 90K glycoprotein are elevated in children with juvenile idiopathic arthritis (JIA) and decrease with etanercept treatment. This suggests 90K may play a role in JIA pathogenesis.
Area of Science:
- Biochemistry
- Immunology
- Pediatric Rheumatology
Background:
- Juvenile idiopathic arthritis (JIA) is a chronic autoimmune disease affecting children.
- Biomarkers are crucial for understanding disease activity and treatment response in JIA.
- 90K glycoprotein is a potential biomarker whose role in JIA requires further investigation.
Purpose of the Study:
- To determine if circulating 90K glycoprotein levels are elevated in children with JIA.
- To compare 90K levels across different JIA disease stages and healthy controls.
- To assess changes in 90K levels following treatment with etanercept, an anti-tumor necrosis factor (TNF) drug.
Main Methods:
- Assessed 90K glycoprotein, C-reactive protein, ESR, and JADAS in 71 children (23 new JIA, 23 active JIA, 25 controls).
- Evaluated patients eligible for anti-TNF therapy with a 6- and 12-month follow-up after etanercept treatment.
- Measured other relevant markers including TNF, antinuclear antibodies, and rheumatoid factor.
Main Results:
- Significantly higher 90K glycoprotein levels were observed in children with JIA at onset compared to established JIA and controls (p < .001).
- Following 12 months of etanercept treatment, 90K levels significantly decreased at 6 months (p = .001) and further declined at 12 months (p < .001).
- Baseline 90K levels were 157.7 μg/ml in new JIA, 90.0 μg/ml in treated JIA, and 58.0 μg/ml in controls.
Conclusions:
- Circulating 90K glycoprotein levels are elevated in children with JIA, indicating a potential pathogenetic role.
- Etanercept therapy over 12 months effectively reduces 90K glycoprotein levels in JIA patients.
- 90K glycoprotein shows promise as a biomarker for disease activity and treatment response in JIA.
Objectives:
To assess whether circulating levels of 90K glycoprotein are increased in children with juvenile idiopathic arthritis (JIA) at different stages of the disease, compared to healthy controls and to evaluate potential over time changes in its concentrations following treatment with the antitumor-necrosis factor (TNF) drug etanercept.
Methods:
90K glycoprotein, C-reactive protein, erythrocyte sedimentation rate, TNF, antinuclear antibodies, rheumatoid factor and the Juvenile Arthritis Disease Activity Score were assessed in 71 children: 23 with newly diagnosed JIA, 23 with established and active JIA and 25 healthy controls. Patients, eligible for anti-TNF treatment, underwent a similar clinical/laboratory assessment after 6- and 12-month etanercept therapy.
Results:
At baseline, significant differences were found in 90K levels between the three study groups: JIA at onset (157.7 [131.4-241.5] μg/ml), JIA on treatment (90.0 [68.8-120.2] μg/ml) and control group (58.0 [44.5-79.0] μg/ml), (p for trend <.001), with the JIA at onset group showing the highest values. In the JIA on treatment group, following one-year etanercept treatment, a significant reduction in 90K was detected already at 6 months (74.3 [56.0-104.1] μg/ml p = .001) and a further decline was observed at 12 months (49.3 [46.0-67.6] μg/ml p < .001).
Conclusion:
Our study showed that 90K glycoprotein levels are increased in JIA children compared to healthy controls, suggesting a potential pathogenetic role in the JIA. Besides, 12 months of therapy with etanercept can reduce 90K levels.
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