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Weight reduction can decrease circulating soluble lectin-like oxidized low-density lipoprotein receptor–1 levels in overweight middle-aged men

机译:减轻体重可以降低超重中年男性的循环可溶性可溶性凝集素样氧化型低密度脂蛋白受体–1水平

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摘要

Circulating soluble lectin-like oxidized low-density lipoprotein receptor–1 (sLOX-1) has been reported to be associated with acute coronary syndrome, but its association with obesity has not been elucidated.In this study, we examined whether weight reduction would reduce the serum levels of sLOX-1 in a 12-week weight reduction intervention. Thirty-eight overweight middle-aged men were enrolled in the study, and 32 completed the intervention. The serum level of sLOX-1 was measured using a chemiluminescent enzyme-linked immunoassay. After the intervention program, bodyweight and the serum level of sLOX-1 decreased significantly (−7.5% ± 4.8% and −72.1% ± 35.9%, respectively). Changes in serum levels of sLOX-1 were positively correlated with changes in body weight ( r = 0.54, P = .003), body mass index (r = 0.57, P = .001), body fat mass (r = 0.57, P = .002), total cholesterol (r = 0.41, P = .03), subcutaneous fat area (r = 0.50, P = .007), high-sensitivity C-reactive protein (r = 0.56, P = .002), leptin (r = 0.47, P = .01), and tumor necrosis factor–α (r = 0.32, P = .09); but no correlations were observed with fasting glycemic-related factors (blood glucose, hemoglobin A1c, and insulin). Changes in body mass index and high-sensitivity C-reactive protein were selected as significant predictors of sLOX-1 changes by multiple regression analyses. These results suggest that LOX-1 induction may be related to adipocyte metabolism, inflammation, and immune response associated with obesity.
机译:据报道,循环性可溶性凝集素样氧化型低密度脂蛋白受体-1(sLOX-1)与急性冠状动脉综合征相关,但尚不清楚与肥胖的相关性。在这项研究中,我们研究了减轻体重是否会减轻体重在为期12周的减重干预措施中检测sLOX-1的血清水平。该研究招募了38名超重中年男性,其中32名完成了干预。 sLOX-1的血清水平使用化学发光酶联免疫法测定。干预计划后,sLOX-1的体重和血清水平显着下降(分别为-7.5%±4.8%和-72.1%±35.9%)。血清sLOX-1水平的变化与体重(r = 0.54,P = .003),体重指数(r = 0.57,P = .001),体脂质量(r = 0.57,P)呈正相关。 = .002),总胆固醇(r = 0.41,P = .03),皮下脂肪区(r = 0.50,P = .007),高敏感性C反应蛋白(r = 0.56,P = .002),瘦素(r = 0.47,P = 0.01)和肿瘤坏死因子-α(r = 0.32,P = .09);但未观察到与空腹血糖相关因素(血糖,血红蛋白A1c和胰岛素)的相关性。通过多次回归分析,选择体重指数和高敏C反应蛋白的变化作为sLOX-1变化的重要预测指标。这些结果表明,LOX-1的诱导可能与肥胖相关的脂肪细胞代谢,炎症和免疫反应有关。

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