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Serum advanced glycation end products (AGEs) are associated with insulin resistance

机译:血清晚期糖基化终末产物(AGEs)与胰岛素抵抗相关

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Background: In addition to the important role of advanced glycation end products (AGEs) in the pathogenesis of diabetic vascular complications, recent data suggest that advanced glycation end products can also impair insulin action in vitro. We have investigated whether circulating advanced glycation end products are associated with insulin resistance in human subjects independent of metabolic parameters. Methods: Two hundred and seven healthy non-obese non-diabetic subjects (97 male, 110 female) were recruited from the community. Serum levels of advanced glycation end products, adiponectin, malondialdehyde and high sensitivity C-reactive protein were assayed. Insulin resistance was determined by the homeostasis model assessment index (HOMA-IR). Results: Male subjects had significantly higher body mass index, waist circumference and lower adiponectin level than female subjects and were more insulin resistant. Serum advanced glycation end products (3.67 ± 1.15 unit/mL versus 3.23 ± 1.15, p < 0.05) and malondialdehyde levels (p < 0.05) were also higher in male than in female subjects. Serum advanced glycation end products correlated with HOMA-IR in both male (r = 0.32, p = 0.004) and female subjects (r = 0.28, p = 0.003). Serum adiponectin inversely correlated with HOMA-IR in female (r = - 0.38, p < 0.001) but not in male subjects. On multiple regression analysis, serum AGEs remained an independent determinant of HOMA-IR even after adjusting for age, gender, body mass index, waist, smoking, adiponectin and markers of oxidative stress and inflammation. Conclusions: Formation and accumulation of advanced glycation end products progress during normal ageing. We have demonstrated that the circulating level of advanced glycation end products is associated with insulin resistance even in non-obese, non-diabetic subjects independent of adiponectin.
机译:背景:除了高级糖基化终末产物(AGEs)在糖尿病血管并发症的发病机理中的重要作用外,最新数据表明,高级糖基化终末产物还可在体外损害胰岛素的作用。我们已经研究了循环高级糖基化终产物是否与人类受试者的胰岛素抵抗相关,而与代谢参数无关。方法:从社区招募了207名健康的非肥胖非糖尿病受试者(男97例,女110例)。测定了晚期糖基化终产物,脂联素,丙二醛和高灵敏度C反应蛋白的血清水平。通过稳态模型评估指数(HOMA-IR)确定胰岛素抵抗。结果:男性受试者的体重指数,腰围和脂联素水平明显高于女性受试者,并且胰岛素抵抗性更高。男性的血清晚期糖基化终产物(3.67±1.15单位/ mL对3.23±1.15,p <0.05)和丙二醛水平(p <0.05)也高于女性。男性(r = 0.32,p = 0.004)和女性(r = 0.28,p = 0.003)的血清晚期糖基化终产物均与HOMA-IR相关。女性血清脂联素与HOMA-IR呈负相关(r =-0.38,p <0.001),而男性受试者则没有。在多元回归分析中,即使在调整了年龄,性别,体重指数,腰围,吸烟,脂联素以及氧化应激和炎症指标后,血清AGEs仍然是HOMA-IR的独立决定因素。结论:正常糖化过程中高级糖基化终产物的形成和积累得以发展。我们已经证明,即使在独立于脂联素的非肥胖,非糖尿病受试者中,晚期糖基化终产物的循环水平也与胰岛素抵抗相关。

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