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DOI 10.1016/j.bbrc.2015.02.018

Медицинская библиотека · Biochemical and biophysical research communications · 2015

Plasma and urinary glycosaminoglycans in the course of juvenile idiopathic arthritis.

Winsz-Szczotka Katarzyna, Kuźnik-Trocha Kornelia, Komosińska-Vassev Katarzyna, Wisowski Grzegorz, Gruenpeter Anna, Lachór-Motyka Iwona, Żegleń Bogusław, Lemski Wojciech, Olczyk Krystyna

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

OBJECTIVES

The aim of the study was to perform analyses of plasma and urinary glycosaminoglycan isolated from juvenile idiopathic arthritis (JIA).

METHODS,

RESULTS

Chondroitin/dermatan sulfate (CS/DS), heparan sulfate/heparin (HS/H) and hyaluronic acid (HA) were evaluated in samples obtained from JIA patients before and after treatment. Electrophoretic analysis of GAGs identified the presence of CS, DS and HS/H in plasma of healthy subjects and JIA patients. CS were the predominant plasma GAGs constituent in all investigated subject. The plasma CS level in untreated patients was significantly decreased. Therapy resulted in an increase in this glycan level. However, plasma CS concentration still remained higher than in controls. Increased levels of DS and HA in untreated JIA patients were recorded. Anti-inflammatory treatment led to normalization of these parameters concentrations. Plasma and urinary concentrations of HS/H were similar in all groups of individuals. Urinary CS/DS and HA were decreased only in untreated patients.

CONCLUSIONS

The data presented indicate that changes in plasma and urinary glycosaminoglycan occur in the course of JIA. There are probably the expression of both local articular cartilage matrix and systemic changes in connective tissue remodeling.

Для цитирования: Winsz-Szczotka Katarzyna, Kuźnik-Trocha Kornelia, Komosińska-Vassev Katarzyna, Wisowski Grzegorz, Gruenpeter Anna, Lachór-Motyka Iwona, Żegleń Bogusław, Lemski Wojciech, Olczyk Krystyna. Plasma and urinary glycosaminoglycans in the course of juvenile idiopathic arthritis.. Biochemical and biophysical research communications. 2015. DOI: 10.1016/j.bbrc.2015.02.018.

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