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Serum profile of transferrin isoforms in juvenile idiopathic arthritis: a preliminary study
Ewa Gruszewska1, Magdalena Sienkiewicz2, Paweł Abramowicz3
1Department of Biochemical Diagnostics, Medical University of Bialystok, Waszyngtona 15A Street, 15-269, Białystok, Poland. gr_ewa@interia.pl.
Insights
Juvenile idiopathic arthritis (JIA) alters serum transferrin glycosylation, with lower tetrasialotransferrin and higher pentasialotransferrin levels observed in patients. These changes may offer clinical utility for JIA assessment.
Area of Science:
- Biochemistry
- Immunology
- Pediatrics
Background:
- Protein glycosylation changes are noted in adult rheumatic diseases, but data on pediatric rheumatic conditions are limited.
- Juvenile idiopathic arthritis (JIA) is a common pediatric rheumatic disease with complex pathogenesis.
- Transferrin, a key serum glycoprotein, undergoes glycosylation that can be altered in various disease states.
Purpose of the Study:
- To investigate the impact of juvenile idiopathic arthritis (JIA) on the serum glycosylation profile of transferrin isoforms.
- To assess potential correlations between transferrin isoform levels and disease activity or disability in JIA patients.
Main Methods:
- Serum samples from 25 active JIA patients and 22 healthy controls were analyzed.
- Capillary electrophoresis using the MINICAP system was employed to quantify transferrin isoforms.
- Disease activity was assessed using JADAS 27, and disability via VAS and CHAQ scores.
Main Results:
- JIA patients exhibited significantly lower tetrasialotransferrin (median 82.6%) and higher pentasialotransferrin (median 14%) levels compared to controls.
- No significant correlations were found between transferrin isoform levels and JIA disease activity scores (JADAS 27) or disability measures (VAS, CHAQ).
- Erythrocyte sedimentation rate and CRP levels showed positive correlations with disialotransferrin and pentasialotransferrin, and negative correlations with trisialotransferrin and tetrasialotransferrin.
Conclusions:
- This preliminary study reveals distinct shifts in the transferrin isoform profile in patients with JIA.
- Measurements of tetrasialotransferrin and pentasialotransferrin may hold potential clinical utility in JIA.
- Further large-scale prospective studies are warranted to validate these findings and explore their clinical applications.
Abstract:
It is reported that alterations in protein glycosylation are present in adult rheumatic diseases; however, the data related to pediatric rheumatic conditions are very scarce. The aim of this study was to assess the effect of juvenile idiopathic arthritis (JIA) on the serum glycosylation profile of transferrin isoforms. Twenty-five patients with different clinical forms of an active JIA and 22 healthy controls were studied. Serum samples were analyzed by capillary electrophoresis on MINICAP electrophoretic system (Sebia, France) to determine the levels of transferrin isoforms. In patients with JIA, tetrasialotransferrin (median 82.6%; range 68.8-99.5) concentration was lower (P = 0.032), and pentasialotransferrin (median 14%; range 0.5-31.2) was higher (P = 0.020) in comparison to controls (median 84.45; range 79.8-87.4; median 11.55; range 9.7-16.1, respectively). No significant correlations between concentration of transferrin isoforms and disease activity score (JADAS 27) or the degree of disability (VAS and CHAQ) were found. Erythrocyte sedimentation rate and CRP levels correlated positively with disialotransferrin (R = 0.493, P = 0.017; R = 0.850, P < 0.001, respectively) and pentasialotransferrin (R = 0.533, P = 0.006; R = 0.491, P = 0.045, respectively), and negatively with trisialotransferrin (R = - 0.546, P = 0.007; R = - 0.515, P = 0.049, respectively) and tetrasialotransferrin (R = - 0.436, P = 0.029; R = - 0.504, P = 0.039, respectively). This preliminary study shows the shifts in transferrin isoforms profile among patients with JIA. Our data indicate a potential clinical utility of the transferrin isoforms measurement, especially tetrasialotransferrin and pentasialotransferrin. Further prospective studies on larger groups of patients should be conducted to validate the results.
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