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首页> 外文期刊>Endocrine journal >Annual change in plasma xanthine oxidoreductase activity is associated with changes in liver enzymes and body weight
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Annual change in plasma xanthine oxidoreductase activity is associated with changes in liver enzymes and body weight

机译:血浆黄嘌呤氧化还原酶活性的年变化与肝酶和体重的变化有关

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Xanthine oxidoreductase (XOR), an enzyme of uric acid formation from hypoxanthine and xanthine, is recognized as a source of oxidative stress. Plasma activity of XOR has been reported to be a biomarker of metabolic disorders associated with obesity, liver dysfunction, insulin resistance, hyperuricemia and adipokines. We investigated longitudinal change in plasma XOR activity, which was determined by using mass spectrometry and liquid chromatography to detect [13C2, 15N2]-uric acid using [13C2, 15N2]-xanthine as a substrate, in 511 subjects (male/female: 244/267) of the Tanno-Sobetsu Study in the years 2016 and 2017. Plasma XOR activity in a basal state was significantly higher in men than in women, but no significant sex difference was observed in annual change in plasma XOR activity. Annual change in plasma activity of XOR was positively correlated with changes in each parameter, including body weight (r = 0.203, p 0.001), body mass index, diastolic blood pressure, aspartate transaminase (AST) (r = 0.772, p 0.001), alanine transaminase (r = 0.647, p 0.001), γ-glutamyl transpeptidase, total cholesterol, triglycerides, uric acid, fasting glucose and HbA1c. Multivariate regression analysis demonstrated that change in AST and that in body weight were independent predictors of change in plasma XOR activity after adjustment of age, sex and changes in each variable with a significant correlation without multicollinearity. In conclusion, annual change in plasma XOR activity is independently associated with changes in liver enzymes and body weight in a general population. Improvement of liver function and reduction of body weight would decrease plasma XOR activity and its related oxidative stress as a therapeutic strategy.
机译:黄嘌呤氧化还原酶(XOR)是一种从缺氧和黄嘌呤形成的尿酸形成的酶,被认为是氧化应激的源。据报道,XOR的血浆活性是与肥胖,肝功能障碍,胰岛素抵抗,高尿酸血症和脂肪因子相关的代谢障碍的生物标志物。我们研究了血浆XOR活性的纵向变化,其通过使用质谱和液相色谱法测定使用[13C2,15N2] - 黄嘌呤作为底物作为底物检测[13C2,15N2] - 尿酸,在511个受试者中(雄性/女性:244 / 267)2016年和2017年的Tanno-Sobetsu研究。男性的血浆XOR活性比女性显着高,但在血浆XOR活动的年度变化中没有观察到显着性差异。 XOR血浆活性的年变化与每个参数的变化呈正相关,包括体重(r = 0.203,p <0.001),体重指数,舒张压,天冬氨酸转氨酶(AST)(r = 0.772,p <0.001 ),丙氨酸转氨酶(R = 0.647,P <0.001),γ-谷氨酸转琥珀酶,总胆固醇,甘油三酯,尿酸,空腹葡萄糖和HBA1C。多元回归分析证明,AST的变化以及体重中的变化是在调整年龄,性别和调整后的血浆XOR活性变化的独立预测因子,每变量的变化具有显着的相关性而无需多含量。总之,血浆XOR活性的年变化与一般人群的肝酶和体重的变化独立相关。肝功能的改善和体重还原会降低血浆XOR活性及其相关的氧化应力作为治疗策略。

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