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Inflammatory biomarkers and oxidative stress measurements in patients with systemic lupus erythematosus with or without metabolic syndrome.

机译:系统性红斑狼疮伴或不伴代谢综合征的患者的炎症生物标志物和氧化应激测量。

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The aims of the present study were to report the frequency of metabolic syndrome in systemic lupus erythematosus (SLE); to verify differences in inflammatory biomarkers and oxidative stress in SLE patients with or without metabolic syndrome; and to assess which metabolic syndrome components are associated with oxidative stress and disease activity. The study included 58 SLE patients and 105 controls. SLE patients were divided in two groups, with and without metabolic syndrome. 41.4% patients met the criteria for metabolic syndrome compared with 10.5% controls. Patients with SLE and metabolic syndrome had significantly raised serum uric acid, C-reactive protein (CRP), lipid hydroperoxides, and protein oxidation when compared with patients with SLE without metabolic syndrome. Lipid hydroperoxides were correlated with CRP, whereas protein oxidation was associated with waist circumference and uric acid. There was a positive association between serum C3 and C4 and glucose and between C3 and CRP. SLE disease activity index (SLEDAI) scores were positively correlated with body mass index (BMI) and waist circumference (WC). In conclusion, SLE patients have a high prevalence of metabolic syndrome and this syndrome directly contributes to increase inflammatory status and oxidative stress. Inflammatory processes, being overweight/obese, and uric acid may favor oxidative stress increases in patients with SLE and metabolic syndrome. C3 and C4 may have a positive acute-phase protein behavior in patients with SLE.
机译:本研究的目的是报告系统性红斑狼疮(SLE)代谢综合征的发生率。验证患有或不患有代谢综合征的SLE患者的炎症生物标志物和氧化应激的差异;并评估哪些代谢综合征成分与氧化应激和疾病活动有关。该研究包括58位SLE患者和105位对照。 SLE患者分为两组,有无代谢综合征。 41.4%的患者符合代谢综合征的标准,而对照组为10.5%。与没有代谢综合征的SLE患者相比,患有SLE和代谢综合征的患者血清尿酸,C反应蛋白(CRP),脂质过氧化氢和蛋白质氧化显着升高。脂质氢过氧化物与CRP相关,而蛋白质氧化与腰围和尿酸相关。血清C3和C4与葡萄糖之间以及C3与CRP之间存在正相关。 SLE疾病活动指数(SLEDAI)得分与体重指数(BMI)和腰围(WC)正相关。总之,SLE患者的代谢综合征患病率很高,该综合征直接导致炎症状态和氧化应激的增加。 SLE和代谢综合症患者的超重/肥胖和尿酸炎症过程可能会促进氧化应激的增加。 SLE患者中C3和C4可能具有积极的急性期蛋白行为。

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