LDL oxidation in patients with severe carotid atherosclerosis. A study of in vitro and in vivo oxidation markers.

E Maggi, R Chiesa, G Melissano, R Castellano, D Astore, A Grossi, G Finardi, G Bellomo
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Abstract

Among the various risk factors involved in the development and progression of carotid atherosclerosis, the oxidation of LDL has been proposed to play a relevant role. LDL oxidation has been investigated in 94 patients with severe carotid atherosclerosis undergoing elective carotid artery endarterectomy and in 42 matched control subjects. LDL oxidation was evaluated in all patients as (1) the susceptibility to in vitro oxidation, (2) vitamin E concentration and its efficiency in LDL, and (3) the presence of autoantibodies against oxidatively modified lipoprotein to monitor the occurrence of the oxidative processes taking place in vivo. No difference was detected between control subjects and patients concerning vitamin E concentration and the kinetics of conjugated diene formation in isolated LDL exposed to CuSO4. However, vitamin E efficiency was lower (9.6 +/- 4.2 versus 30.2 +/- 7.6 min/nmol vitamin E) and the duration of the vitamin E-independent lag phase was longer (105.5 +/- 16.5 versus 58 +/- 11.8 minutes) in the patient group. Autoantibodies against oxidatively modified lipoproteins were measured with an ELISA method using native LDL, Cu(2+)-oxidized LDL (oxLDL), or malondialdehyde-derivatized LDL (MDA-LDL) as antigens. To monitor cross-reactivity of the antibodies detected with other oxidatively modified proteins, human serum albumin (HSA) and MDA-derivatized HSA (MDA-HSA) were also employed. The antibody titer was calculated as the ratio of antibodies against modified versus native proteins.(ABSTRACT TRUNCATED AT 250 WORDS)

重度颈动脉粥样硬化患者LDL氧化。体外和体内氧化标志物的研究。
在参与颈动脉粥样硬化发生发展的多种危险因素中,LDL氧化已被认为发挥了相关作用。在94名接受选择性颈动脉内膜切除术的严重颈动脉粥样硬化患者和42名匹配的对照组中研究了LDL氧化。对所有患者的LDL氧化进行评估,包括(1)对体外氧化的敏感性,(2)维生素E浓度及其在LDL中的效率,以及(3)抗氧化修饰脂蛋白自身抗体的存在,以监测体内氧化过程的发生。在暴露于CuSO4的分离LDL中维生素E浓度和共轭二烯形成动力学方面,对照组和患者之间没有发现差异。然而,患者组维生素E效率较低(9.6 +/- 4.2 vs 30.2 +/- 7.6 min/nmol维生素E),维生素E独立滞后期持续时间较长(105.5 +/- 16.5 vs 58 +/- 11.8分钟)。采用ELISA法检测抗氧化修饰脂蛋白的自身抗体,采用天然LDL、Cu(2+)氧化LDL (oxLDL)或丙二醛衍生LDL (MDA-LDL)作为抗原。为了监测检测到的抗体与其他氧化修饰蛋白的交叉反应性,还采用了人血清白蛋白(HSA)和mda衍生的HSA (MDA-HSA)。抗体滴度计算为针对修饰蛋白和天然蛋白的抗体的比率。(摘要删节250字)
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