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HDL-cholesterol: is it really good? Differences between apoA-I and HDL.

机译:HDL-胆固醇:真的很好吗? apoA-I和HDL之间的差异。

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摘要

Since the very first report showing the regression of established atherosclerotic lesions by means of high-density lipoprotein cholesterol (HDL-C) plasma fraction, much information has been generated about the protective role of HDL-C in atherosclerosis. Nonetheless, this positive point of view about HDL has been nearly surpassed since modern informations concerning torcetrapib have appeared. Disappointment was palpable when its pivotal morbidity-and-mortality clinical trial, ILLUMINATE, was abruptly stopped due to excess mortality amongst the group randomized to receive torcetrapib. In this work we will try to put things in perspective. Lowering low-density lipoprotein cholesterol (LDL-C) levels with statins is a proven strategy for reducing the cardiovascular disease (CVD) risk. Despite the impressive benefits of statins, there remain a significant proportion of treated patients in which cardiovascular events are not prevented. Low HDL-C levels are an important independent risk factor for CVD. There is a need to develop suitable therapies to reduce this residual risk through HDL-C related mechanisms. Therefore, we will first review HDL-C pathways and we will subsequently state the new pharmacological approaches to HDL-C metabolism.
机译:自从第一个报告显示通过高密度脂蛋白胆固醇(HDL-C)血浆组分消退已建立的动脉粥样硬化病变以来,已经产生了许多有关HDL-C在动脉粥样硬化中的保护作用的信息。然而,自从有关torcetrapib的现代信息出现以来,关于HDL的积极观点已几乎被超越。当其关键的发病率和死亡率临床试验ILLUMINATE因死亡率过高而突然终止时,令人感到失望。在这项工作中,我们将尝试着眼于事物。他汀类药物降低低密度脂蛋白胆固醇(LDL-C)水平是降低心血管疾病(CVD)风险的行之有效的策略。尽管他汀类药物具有令人印象深刻的好处,但仍有很大一部分接受治疗的患者无法预防心血管事件。低HDL-C水平是CVD的重要独立危险因素。需要开发合适的疗法以通过HDL-C相关机制降低这种残余风险。因此,我们将首先回顾HDL-C途径,然后我们将阐述HDL-C代谢的新药理学方法。

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