首页> 外文期刊>Free radical research >Oxidative stress biomarkers in the serum and plasma of patients with non-alcoholic fatty liver disease (NAFLD). Can plasma AGE be a marker of NAFLD? Oxidative stress biomarkers in NAFLD patients
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Oxidative stress biomarkers in the serum and plasma of patients with non-alcoholic fatty liver disease (NAFLD). Can plasma AGE be a marker of NAFLD? Oxidative stress biomarkers in NAFLD patients

机译:非酒精脂肪肝病(NAFLD)血清和血浆血清和血浆中的氧化应激生物标志物。 血浆年龄可以是nafld的标志吗? NAFLD患者的氧化应激生物标志物

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Still little is known about the redox abnormalities in patients with non-alcoholic fatty liver disease (NAFLD). The purpose of the study was to find the relationship between enzymatic and non-enzymatic antioxidants, redox homeostasis and oxidative damage in 67-patients with NAFLD. The study population was divided into patients with non-alcoholic fatty liver (early NAFLD, n = 29) and patients with non-alcoholic steatohepatitis (advanced NAFLD, n = 38). Redox biomarkers: enzymatic antioxidants (Cu - Zn-superoxide dismutase (SOD), catalase (CAT), glutathi-one peroxidase (GPx), glutathione reductase (GR)); non-enzymatic antioxidants and redox status (reduced glutathione (GSH), total antioxidant capacity (TAC)); and oxidative damage products (total oxidant status (TOS), advanced glycation end products (AGE), malondialdehyde (MDA), and DNA/RNA oxidative damage) were determined in the serum/plasma samples. The activity of SOD, GPx, GR and levels of GSH, TOS, AGE, MDA, and DNA/RNA oxidative damage were significantly elevated in early NAFLD and advanced NAFLD group compared to controls (p<.001). There was a positive correlation between AGE, TAC and ALT activity (R = 0.34, p = .04; R = 0.36, p = .03, respectively) in advanced NAFLD group. Interestingly, ROC analysis for AGE showed good discriminatory ratio for patients with minimal steatosis (BARD score 0-1) vs. moderate steatosis (BARD score 2-4), AUC = 0.76. Plasma AGE can be a potential non-invasive biomarker differentiating NAFLD patients.
机译:关于非酒精性脂肪肝疾病(NAFLD)患者的氧化还原异常仍然很少。该研究的目的是寻找酶促和非酶促抗氧化剂,氧化还原稳态和67例NAFLD患者氧化损伤之间的关系。该研究人群分为非酒精性脂肪肝(早期NAFLD,N = 29)的患者和非酒精性脱脂性患者(晚期NAFLD,N = 38)。氧化还原生物标志物:酶促抗氧化剂(Cu - Zn-超氧化物歧化酶(SOD),过氧化氢酶(猫),谷胱甘肽 - 一度过氧化物酶(GPX),谷胱甘肽还原酶(GR));非酶促抗氧化剂和氧化还原状态(降低谷胱甘肽(GSH),总抗氧化容量(TAC));和氧化损伤产品(总氧化剂状态(TOS),先进的糖化末端产物(年龄),血清/血浆样品中测定丙炔醛(MDA)和DNA / RNA氧化损伤)。与对照相比,早期NAFLD和先进的NAFLD组早期,GSH,TOS,AGE,MDA和DNA / RNA氧化损伤的SOD,GPX,GR和DNA / RNA氧化损伤的活性显着升高(P <.001)。年龄,TAC和ALT活动之间存在正相关(r = 0.34,p = .04; r = 0.36,p = .03)在高级NAFLD组中。有趣的是,ROC AGE分析对于最小的脂肪变性(BARD得分0-1)与中度脂肪变性(BARD得分2-4),AUC = 0.76,患者对年龄的歧视性比例良好。血浆年龄可以是潜在的非侵入性生物标志物,区分NAFLD患者。

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