Lan Nick S R, Watts Gerald F
Medical School, The University of Western Australia.
Department of Cardiology, Fiona Stanley Hospital.
Curr Opin Endocrinol Diabetes Obes. 2025 Apr 1;32(2):66-74. doi: 10.1097/MED.0000000000000879. Epub 2024 Aug 2.
The causal role of high-density lipoprotein (HDL) in atherosclerotic cardiovascular disease (CVD) remains debated. Considering recent evidence, the purpose of this review is to a provide a focused update and new perspectives on HDL and CVD.
A Mendelian randomization study demonstrated an increased risk of CVD when HDL-cholesterol was predominantly transported in larger HDL particles and a decreased risk of CVD when HDL-cholesterol was predominantly transported in smaller HDL particles. Moreover, another Mendelian randomization study demonstrated that concentration and content of medium HDL particles is associated with CVD. A Mendelian randomization study that utilized stratified analyses demonstrated that individuals with HDL-cholesterol 50 mg/dl or less were at increased risk of CVD. Lastly, the AEGIS-II trial demonstrated that CSL112, a human apolipoprotein A-I that increases cholesterol efflux, did not significantly reduce cardiovascular events in patients at very high risk. Exploratory analyses showed that patients treated with CSL112 had numerically lower rates of cardiovascular events.
Qualitative markers of HDL may be causally related to CVD. There is a need for ongoing research into HDL therapeutics that promote the biological properties of HDL. The optimal cohort or disease state that will benefit from these therapies needs to be identified.
高密度脂蛋白(HDL)在动脉粥样硬化性心血管疾病(CVD)中的因果作用仍存在争议。鉴于最近的证据,本综述的目的是提供关于HDL与CVD的重点更新内容及新观点。
一项孟德尔随机化研究表明,当HDL胆固醇主要在较大的HDL颗粒中运输时,CVD风险增加;而当HDL胆固醇主要在较小的HDL颗粒中运输时,CVD风险降低。此外,另一项孟德尔随机化研究表明,中等大小HDL颗粒的浓度和含量与CVD有关。一项采用分层分析的孟德尔随机化研究表明,HDL胆固醇水平为50mg/dl或更低的个体患CVD的风险增加。最后,AEGIS-II试验表明,CSL112(一种可增加胆固醇流出的人载脂蛋白A-I)在极高风险患者中并未显著降低心血管事件。探索性分析显示,接受CSL112治疗的患者心血管事件发生率在数值上较低。
HDL的定性标志物可能与CVD存在因果关系。需要对促进HDL生物学特性的HDL治疗方法进行持续研究。需要确定能从这些治疗中获益的最佳队列或疾病状态。