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高胆固醇血症患者血浆中胆固醇酯转移加速。

Accelerated cholesteryl ester transfer in plasma of patients with hypercholesterolemia.

作者信息

Bagdade J D, Ritter M C, Subbaiah P V

机构信息

Department of Medicine, Rush Medical College, Chicago, Illinois 60612.

出版信息

J Clin Invest. 1991 Apr;87(4):1259-65. doi: 10.1172/JCI115127.

Abstract

To discern the mechanism(s) that underlie abnormal cholesteryl ester transfer (CET) in patients with hypercholesterolemia, we have studied this dysfunctional step in reverse cholesterol transport in 13 subjects with genetically heterogeneous forms of hypercholesterolemia (HC). In all HC patients, the mass of CE transferred in whole plasma from HDL to VLDL and LDL increased rapidly initially and was significantly greater than in controls at 1, 2, and 4 h (P less than 0.005). To further characterize this disturbance, we performed a series of recombination experiments. Combining HC d less than 1.063 containing acceptor VLDL + LDL with the d greater than 1.063 fraction from controls containing donor HDL + CE-transfer protein (CETP) and not the converse combination showed the same characteristics of accelerated CET noted with intact HC plasma, indicating that abnormal transfer was associated with the HC acceptor lipoproteins. When HC VLDL and its subfractions and LDL were isolated separately and then combined with control d greater than 1.063 fractions, accelerated CET was only associated with VLDL1. Consistent with an acceleration of the neutral lipid transfer reaction occurring between HDL and VLDL1 in HC in vivo, we found that the triglyceride/CE ratio was decreased in HC VLDL1 (P less than 0.001), and increased in HDL (P less than 0.25). CETP mass was significantly increased in HC plasma (HC 2.3 +/- 4 micrograms/ml vs. control 1.3 +/- 0.3 micrograms/ml; mean +/- SD; P less than 0.025). This series of observations demonstrate that CET is accelerated in the plasma of HC patients, and this disturbance results from dysfunction of the VLDL1 subfraction rather than an elevation of CETP levels. Since an abnormality of this type in vivo can lead to the accumulation of potentially atherogenic CE-enriched apoB-containing lipoproteins in plasma, it may be an additional previously unrecognized factor that increases cardiovascular risk in HC patients.

摘要

为了探究高胆固醇血症患者胆固醇酯转运(CET)异常的潜在机制,我们对13例具有基因异质性高胆固醇血症(HC)的受试者进行了逆向胆固醇转运中这一功能失调步骤的研究。在所有HC患者中,从高密度脂蛋白(HDL)转移至极低密度脂蛋白(VLDL)和低密度脂蛋白(LDL)的全血浆中胆固醇酯(CE)的量最初迅速增加,且在1小时、2小时和4小时时显著高于对照组(P<0.005)。为了进一步明确这种紊乱情况,我们进行了一系列重组实验。将密度小于1.063的含受体VLDL + LDL的HC与密度大于1.063的含供体HDL + 胆固醇酯转运蛋白(CETP)的对照组组分相结合,而非相反的组合,显示出与完整HC血浆中相同的CET加速特征,表明异常转运与HC受体脂蛋白有关。当分别分离出HC的VLDL及其亚组分和LDL,然后与密度大于1.063的对照组组分相结合时,CET加速仅与VLDL1相关。与体内HC中HDL和VLDL1之间发生的中性脂质转移反应加速一致,我们发现HC的VLDL1中甘油三酯/胆固醇酯比值降低(P<0.001),而HDL中该比值升高(P<0.25)。HC血浆中CETP质量显著增加(HC为2.3±4微克/毫升,对照组为1.3±0.3微克/毫升;均值±标准差;P<0.025)。这一系列观察结果表明,HC患者血浆中的CET加速,且这种紊乱是由VLDL1亚组分功能失调引起的,而非CETP水平升高所致。由于体内这种类型的异常可导致血浆中潜在致动脉粥样硬化的富含CE的载脂蛋白B的脂蛋白积累,它可能是增加HC患者心血管风险的一个此前未被认识的额外因素。

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