Biochemical markers of oxidative stress in patients with inflammatory bowel diseases

G. Mierzwa, J. Budzyński, D. Kupczyk, B. Augustyńska
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Abstract

Introduction: Inflammatory bowel disease (IBD) is a group of diseases of unexplained aetiology, charac - terized by periods of remissions and exacerbations. Reactive oxygen species (ROS) as far as disorders of balance between levels of prooxidants and antioxidants may also participate in the occurrence of IBD. The aim of the present study was an assessment of the antioxidative barrier of the organism in patients with inflammatory bowel disease. Material and methods: The study group consisted of 99 patients (80 with IBD as a study group and 19 healthy as a control group) from Jan Biziel University Hospital in Bydgoszcz, Poland. Venous blood was the material for biochemical analysis: HT, GSH, GPX p , GPX RBC , GST, GR, SOD-1, MDA, NO 2/NO 3-and CP. Results: There were statistically significant differences in oxidative stress parameters observed between the study group and the control group, especially concerning HT, GSH, GPX RBC , GST, SOD-1, MDA and NO 2/NO 3. Discussion: The assumption that increased activity of antioxidative compounds may constitute a defence against the influence of oxidative stress may be true. Their decreased activity may participate in lowering an organism’s abilities to defend against oxidative stress and cause the development of free radical diseases. Further studies into targeted preventive strategies are needed. Conclusions: Prooxidative factors play an essential role in the pathogenesis of IBD. Due to the still un - known etiopathology of IBD, research on imbalances between pro-oxidants and antioxidants should be continued in larger groups of patients.
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炎症性肠病患者氧化应激的生化标志物
简介:炎症性肠病(IBD)是一组病因不明的疾病,其特点是有缓解期和加重期。活性氧(ROS)以及促氧化剂和抗氧化剂水平失衡也可能参与IBD的发生。本研究的目的是评估炎症性肠病患者机体的抗氧化屏障。材料和方法:研究组包括来自波兰比得哥什的Jan Biziel大学医院的99例患者(80例IBD患者作为研究组,19例健康患者作为对照组)。静脉血作为生化分析的材料:HT、GSH、GPX p、GPX RBC、GST、GR、SOD-1、MDA、NO 2/NO 3、CP。结果:研究组与对照组氧化应激参数差异有统计学意义,尤其是HT、GSH、GPX RBC、GST、SOD-1、MDA、NO 2/NO 3。讨论:抗氧化化合物活性增加可能构成抵抗氧化应激影响的假设可能是正确的。它们的活性降低可能参与降低生物体抵御氧化应激的能力,并导致自由基疾病的发展。需要进一步研究有针对性的预防战略。结论:促氧化因子在IBD发病过程中起重要作用。由于IBD的病因尚不清楚,对促氧化剂和抗氧化剂之间失衡的研究应在更大的患者群体中继续进行。
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