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首页> 外文期刊>Clinical Endocrinology >Lipid-lowering therapy does not affect the postprandial drop in high density lipoprotein-cholesterol (HDL-c) plasma levels in obese men with metabolic syndrome: a randomized double blind crossover trial.
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Lipid-lowering therapy does not affect the postprandial drop in high density lipoprotein-cholesterol (HDL-c) plasma levels in obese men with metabolic syndrome: a randomized double blind crossover trial.

机译:降脂治疗不会影响代谢综合征肥胖男性的餐后高密度脂蛋白胆固醇(HDL-c)血浆水平下降:一项随机双盲交叉试验。

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摘要

Introduction The postprandial lipid metabolism in metabolic syndrome patients is disturbed and may add to the increased cardiovascular risk in these patients. It is not known whether postprandial high density lipoprotein-cholesterol (HDL-c) metabolism is also affected and whether this can be influenced by statin and/or ezetimibe treatment. Methods Prospective, randomized, double blind, crossover trial comparing simvastatin 80 mg with simvastatin/ezetimibe 10 mg/10 mg treatment for 6 weeks on postprandial HDL-c metabolism in 15, nonsmoking, male, obese metabolic syndrome patients (Adult Treatment Panel III, ATPIII). Only study medication was allowed. HDL-c concentrations, cholesteryl ester transfer (CET), CET protein (CETP) mass and adiponectin were measured before and after oral fat loading. ClinicalTrials.gov NCT00189085. Results Plasma HDL-c levels remained stable during continuous fasting following an overnight fast. Pre-fat load HDL-c concentrations without treatment, after simvastatin and simvastatin/ezetimibe treatment were 1.15 +/- 0.04, 1.16 +/- 0.05 and 1.11 +/- 0.04 mmol/l. Fat load induced a 11% drop in HDL-c plasma levels; 1.02 +/- 0.05 mmol/l (P < 0.001) which was not affected by either therapy. Triglyceride levels during fat load were similar after both treatments. Total CET increased from 9.73 +/- 0.70 to 12.20 +/- 0.67 nmol/ml/h (P = 0.004). Four hours after fat loading CETP mass was increased while adiponectin levels were decreased, irrespective of treatment. Discussion HDL-c levels decrease as CET increases after fat loading in obese metabolic syndrome patients. This is not influenced by either simvastatin or simvastatin/ezetimibe treatment. After fat loading, CETP mass and CET increased, and adiponectin decreased pointing towards a potential role for intra-abdominal fat. Decreased postprandial HDL-c levels may contribute to the increased cardiovascular risk in metabolic syndrome patients on top of already low HDL-c levels.
机译:简介代谢综合征患者的餐后脂质代谢紊乱,可能增加这些患者的心血管风险。尚不清楚餐后高密度脂蛋白胆固醇(HDL-c)的代谢是否也会受到影响,他汀类药物和/或依泽替米贝治疗是否会影响这种代谢。方法采用前瞻性,随机,双盲,交叉试验,对15名非吸烟,男性,肥胖代谢综合征患者的餐后HDL-c代谢进行比较,比较辛伐他汀80 mg与辛伐他汀/依泽替米贝10 mg / 10 mg治疗6周的情况(成人治疗小组III, ATPIII)。只允许研究药物。在口服脂肪之前和之后测量HDL-c浓度,胆固醇酯转移(CET),CET蛋白(CETP)质量和脂联素。 ClinicalTrials.gov NCT00189085。结果禁食过夜后,连续禁食期间血浆HDL-c水平保持稳定。辛伐他汀和辛伐他汀/依泽替米贝治疗后未经处理的脂肪前HDL-c浓度为1.15 +/- 0.04、1.16 +/- 0.05和1.11 +/- 0.04 mmol / l。脂肪负荷导致HDL-c血浆水平下降11%; 1.02 +/- 0.05 mmol / l(P <0.001),不受任何一种疗法的影响。两种治疗后脂肪负荷期间的甘油三酸酯水平相似。总CET从9.73 +/- 0.70增加到12.20 +/- 0.67 nmol / ml / h(P = 0.004)。与治疗无关,脂肪负荷后四小时,CETP质量增加,而脂联素水平降低。讨论在肥胖代谢综合征患者中,脂肪负荷后HDL-c水平随着CET的增加而降低。这不受辛伐他汀或辛伐他汀/依泽替米贝治疗的影响。脂肪加载后,CETP质量和CET增加,脂联素减少,表明腹内脂肪具有潜在作用。除了已经很低的HDL-c水平外,餐后HDL-c水平的降低可能导致代谢综合征患者的心血管风险增加。

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