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青少年特发性关节炎中聚集蛋白聚糖周转的实验室指标

Laboratory Indicators of Aggrecan Turnover in Juvenile Idiopathic Arthritis.

作者信息

Winsz-Szczotka Katarzyna, Kuźnik-Trocha Kornelia, Komosińska-Vassev Katarzyna, Jura-Półtorak Agnieszka, Olczyk Krystyna

机构信息

Department of Clinical Chemistry and Laboratory Diagnostics, Faculty of Pharmacy with the Division of Laboratory Medicine, Medical University of Silesia, Ulica Jedności 8, 41-200 Sosnowiec, Poland.

出版信息

Dis Markers. 2016;2016:7157169. doi: 10.1155/2016/7157169. Epub 2016 Jan 27.

Abstract

OBJECTIVES

Evaluation of chondroitin sulfate (CS), as an early marker of aggrecan degradation, and chondroitin sulfate 846 epitope (CS846), as a biomarker of CS synthesis, is an attempt at answering the question whether the therapy used in juvenile idiopathic arthritis (JIA) patients contributes to the normalization of biochemical changes in aggrecan.

METHODS AND RESULTS

Serum levels of CS and CS846 as well as catalase (CT), superoxide dismutase (SOD), and glutathione peroxidase (GPx) activities in erythrocyte were assessed in patients before and after treatment. In the course of JIA, aggrecan metabolism is disturbed, which is reflected by a decrease (p < 0.001) in CS serum level and an increase (p < 0.05) in CS846 concentration. Furthermore, increased (p < 0.001) activities of CT, SOD, and GPx in untreated JIA patients were recorded. The anti-inflammatory treatment resulted in the normalization of CS846 level and SOD and GPx activities. In untreated patients, we have revealed a significant correlation between serum CS and CS846, CT, CRP, ESR, MMP-3, and ADAMTS-4, respectively, as well as between CS846 and CT, GPx, CRP, ESR, and TGF-β1, respectively.

CONCLUSION

The observed changes of CS and CS846 in JIA patients indicate a further need of the therapy continuation aimed at protecting a patient from a possible disability.

摘要

目的

评估硫酸软骨素(CS)作为聚集蛋白聚糖降解的早期标志物,以及硫酸软骨素846表位(CS846)作为CS合成的生物标志物,旨在回答青少年特发性关节炎(JIA)患者所采用的治疗方法是否有助于聚集蛋白聚糖生化变化正常化这一问题。

方法与结果

在治疗前后对患者血清中CS和CS846的水平以及红细胞中过氧化氢酶(CT)、超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GPx)的活性进行评估。在JIA病程中,聚集蛋白聚糖代谢受到干扰,这表现为CS血清水平降低(p < 0.001)以及CS846浓度升高(p < 0.05)。此外,未治疗的JIA患者CT、SOD和GPx的活性增加(p < 0.001)。抗炎治疗使CS846水平以及SOD和GPx的活性恢复正常。在未治疗的患者中,我们分别发现血清CS与CS846、CT、CRP、ESR、MMP - 3和ADAMTS - 4之间,以及CS846与CT、GPx、CRP、ESR和TGF -β1之间存在显著相关性。

结论

JIA患者中观察到的CS和CS846变化表明,进一步需要持续进行治疗,以防止患者可能出现残疾。

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