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Antioxidant profile in patients with complex regional pain syndrome type I

机译:I型复杂性局部疼痛综合征患者的抗氧化特性

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Objective: Complex regional pain syndrome (CRPS) type I is one of the most important problems with regard to physical medicine and rehabilitation. CRPS may cause not only higher therapeutic costs but also greater work time loss. The mechanism and pathogenesis of CRPS still remains unknown. Some findings indicating oxidative stress have been reported. This study was carried out to determine the role of oxidative stress in patients with CRPS. Materials and methods: Twenty patients (13 women and seven men) with CRPS and 20 age- and sex-matched healthy controls were enrolled in this study. Complex regional pain syndrome was diagnosed according to the modified International Association for the Study of Pain (IASP) criteria. We evaluated demographic, clinical and laboratory characteristics of the patients. Antioxidant enzymatic activities consisting of serum superoxide dismutase (SOD), glutathion peroxidase (GPX) and glutathione S-transferase (GST) activities were measured using appropriate methods and compared with healthy controls. Results: The mean age of the patients was 39.5 years and the mean duration of symptoms was 5.5 months. Complex regional pain syndrome devoleped after a traumatic event in 90% of patients. In 10% of patients there were no traumatic events. SOD, GPX and GST levels were significantly higher in patients with CRPS than healthy controls (P = 0.012, P = 0.036 and P = 0.016, respectively). Conclusion: Our findings suggest a possible role of oxidative stress in the pathogenesis of CRPS.
机译:目的:I型复杂区域性疼痛综合征(CRPS)是物理医学和康复领域最重要的问题之一。 CRPS不仅会导致更高的治疗费用,而且会导致更大的工作时间损失。 CRPS的机制和发病机制仍然未知。已经报道了一些表明氧化应激的发现。进行这项研究来确定氧化应激在CRPS患者中的作用。材料和方法:这项研究招募了20名CRPS患者(13名女性和7名男性)和20名年龄和性别相匹配的健康对照。根据修改后的国际疼痛研究协会(IASP)标准诊断出复杂的区域性疼痛综合征。我们评估了患者的人口统计学,临床和实验室特征。使用适当的方法测量了由血清超氧化物歧化酶(SOD),谷胱甘肽过氧化物酶(GPX)和谷胱甘肽S-转移酶(GST)活性组成的抗氧化酶活性,并与健康对照进行了比较。结果:患者的平均年龄为39.5岁,平均症状持续时间为5.5个月。 90%的患者在创伤事件后消失了复杂的局部疼痛综合征。在10%的患者中没有创伤事件。 CRPS患者的SOD,GPX和GST水平显着高于健康对照组(分别为P = 0.012,P = 0.036和P = 0.016)。结论:我们的发现提示氧化应激可能在CRPS的发病机理中发挥作用。

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