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NOX2-generated oxidative stress is associated with severity of ultrasound liver steatosis in patients with non-alcoholic fatty liver disease

机译:非酒精性脂肪肝患者中NOX2产生的氧化应激与超声肝脂肪变性的严重程度有关

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Background Chronic oxidative stress is one of the key mechanisms responsible for disease progression in non-alcoholic fatty liver disease. However, so far, few studies reported increased circulating levels of oxidative stress markers in patients with non-alcoholic fatty liver and no study has been performed with newer markers of systemic oxidative stress. The aim was to assess the relationship between urinary 8-iso-prostaglandin F2α and serum soluble NOX2-derived peptide and the severity of liver steatosis in subjects with non-alcoholic fatty liver. Methods The study was performed in 264 consecutive patients referred for suspected metabolic disease. Steatosis was defined according to Hamaguchi ultrasonographic criteria. Oxidative stress was assessed by urinary 8-iso- prostaglandin F2α and serum soluble NOX2-derived peptide levels. Results Patients with non-alcoholic fatty liver had higher (p? Conclusions We demonstrated increased markers of oxidative stress in subjects with non-alcoholic fatty liver. Urinary 8-iso-PGF2α and serum soluble NOX2-derived peptide levels were independent from obesity, diabetes and metabolic syndrome and increased with the severity of liver steatosis at ultrasound.
机译:背景技术慢性氧化应激是导致非酒精性脂肪肝疾病进展的关键机制之一。然而,到目前为止,很少有研究报道非酒精性脂肪肝患者的氧化应激标志物的循环水平增加,并且还没有使用较新的系统性氧化应激标志物进行研究。目的是评估非酒精性脂肪肝患者尿中8-异前列腺素F2α和血清可溶性NOX2衍生肽与肝脂肪变性严重程度之间的关系。方法本研究在264名被怀疑患有代谢疾病的连续患者中进行。根据Hamaguchi超声检查标准定义脂肪变性。通过尿中的8-异前列腺素F2α和血清可溶性NOX2衍生的肽水平评估了氧化应激。结果非酒精性脂肪肝患者的血脂水平较高(p?结论)我们证明了非酒精性脂肪肝患者的氧化应激指标增加。尿中的8-iso-PGF2α和血清可溶性NOX2衍生的肽水平与肥胖,糖尿病无关代谢综合征,并随着超声检查肝脏脂肪变性的严重程度增加。

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