Związek wysokiego osoczowego stężenia progranuliny ze stężeniem glikozoaminoglikanów, jako biochemicznych wskaźników proteolityczo-prooksydacyjnej modyfikacji agrekanu, w przebiegu młodzieńczego idiopatycznego zapalenia stawów

ORYGINALNY ARTYKUŁ

Związek wysokiego osoczowego stężenia progranuliny ze stężeniem glikozoaminoglikanów, jako biochemicznych wskaźników proteolityczo-prooksydacyjnej modyfikacji agrekanu, w przebiegu młodzieńczego idiopatycznego zapalenia stawów

Katarzyna Winsz-Szczotka 1 , Kornelia Kuźnik-Trocha 1 , Katarzyna Komosińska-Vassev 1 , Wojciech Lemski 1 , Krystyna Olczyk 1

1. Department of Clinical Chemistry and Laboratory Diagnostics, Faculty of Pharmacy with the Division of Laboratory Medicine in Sosnowiec, Medical University of Silesia, Sosnowiec, Poland

Opublikowany: 2018-10-25
DOI: 10.5604/01.3001.0012.6949
GICID: 01.3001.0012.6949
Dostępne wersje językowe: pl en
Wydanie: Postepy Hig Med Dosw 2018; 72 : 906-912

 

Abstrakt

Aim: Progranulin (PGRN) plays an important role in cartilage metabolism. The disturbed interaction between PGRN and glycosaminoglycans (GAGs), as biochemical indicators of aggrecan modification, may contribute to articular damage observed in the course of juvenile idiopathic arthritis (JIA). Hence, the aim of this study was to assess quantitatively the level of progranulin in children with JIA as well as to evaluate the correlation between PGRN and GAGs, MMP-3 (matrix metalloproteinase 3), ADAMTS-4 (a disintegrin and metalloproteinase with thrombospondin motifs 4) as well as the total oxidative status (TOS) and the total antioxidative status (TAS). We have also evaluated interactions between PGRN and inflammatory and anemia indicators, i.e. C-reactive protein (CRP), and hemoglobin (Hb), respectively. Material/Methods: The PRGN level was measured using the immunoenzymatic method, in blind tested coded plasma samples, obtained from both JIA patients before and after treatment and from healthy children. Results: Increased (p<0.001) plasma progranulin in JIA patients before treatment was observed. Therapy resulted in a decrease in the PRGN level. However, the plasma PRGN level still remained higher (p<0.05) than in the controls. In both groups of patients, we have revealed an insignificant correlation between plasma PGRN and GAGs levels. Moreover, a significant correlation between plasma PGRN level and MMP-3, ADAMTS-4, TOS, TAS, CRP and Hb levels, was stated in untreated JIA patients. Conclusions: The obtained results may indicate that PGRN has antioxidative properties in the course of JIA, but do not confirm the protective roles of this glycoprotein in respect to the destructive effects of proteolytic factors.

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