University of Patras, School of Medicine, Department of Pharmacology, Rio Achaias, TK 26500, Greece.
University of Patras, School of Medicine, Department of Pharmacology, Rio Achaias, TK 26500, Greece; European University Cyprus, Department of Life Sciences, School of Sciences, Nicosia, Cyprus.
Vascul Pharmacol. 2021 Dec;141:106928. doi: 10.1016/j.vph.2021.106928. Epub 2021 Oct 22.
Epidemiological studies during the last five years suggest that a relation between high density lipoprotein cholesterol (HDL-C) levels and the risk for cardiovascular disease (CVD) does exist but follows rather a "U-shaped" curve with an optimal range of HDL-C concentration between 40 and 70 mg/dl for men and 50-70 mg/dl for women. Moreover, as research in the field of lipoproteins progresses it becomes increasingly apparent that HDL particles possess different attributes and depending on their structural and functional characteristics, they may be "antiatherogenic" or "proatherogenic". In light of this information, it is highly doubtful that the choice of experimental drugs and the design of respective clinical trials that put the HDL-C raising hypothesis at test, were the most suitable. Here, we compile the existing literature on HDL, providing a critical up-to-date view that focuses on key data from the biochemistry, epidemiology and pharmacology of HDL, including data from clinical trials. We also discuss the most up-to-date information on the contribution of HDL structure and function to the prevention of atherosclerosis. We conclude by summarizing important differences between mouse models and humans, that may explain why pharmacological successes in mice turn out to be failures in humans.
在过去五年的流行病学研究表明,高密度脂蛋白胆固醇(HDL-C)水平与心血管疾病(CVD)风险之间确实存在关系,但遵循的是“U 型”曲线,男性的最佳 HDL-C 浓度范围为 40-70mg/dl,女性为 50-70mg/dl。此外,随着脂蛋白领域的研究进展,越来越明显的是,HDL 颗粒具有不同的特性,根据其结构和功能特性,它们可能具有“抗动脉粥样硬化”或“促动脉粥样硬化”作用。有鉴于此,人们高度怀疑选择实验药物和设计各自的临床试验来检验 HDL-C 升高假说是否最合适。在这里,我们编译了现有的关于 HDL 的文献,提供了一个批判性的最新观点,重点关注 HDL 的生物化学、流行病学和药理学的关键数据,包括临床试验的数据。我们还讨论了 HDL 结构和功能对预防动脉粥样硬化的最新信息。最后,我们总结了小鼠模型和人类之间的重要差异,这些差异可能解释了为什么在小鼠中药物治疗的成功在人类中却失败了。