Department of Internal Medicine, Division of Cardiology, University of Texas Southwestern Medical Center, Dallas (A. Rohatgi).
Department of Pediatrics, Section Molecular Genetics, University Medical Center Groningen, University of Groningen, The Netherlands (M.W.).
Circulation. 2021 Jun 8;143(23):2293-2309. doi: 10.1161/CIRCULATIONAHA.120.044221. Epub 2021 Jun 7.
Low high-density lipoprotein cholesterol (HDL-C) characterizes an atherogenic dyslipidemia that reflects adverse lifestyle choices, impaired metabolism, and increased cardiovascular risk. Low HDL-C is also associated with increased risk of inflammatory disorders, malignancy, diabetes, and other diseases. This epidemiologic evidence has not translated to raising HDL-C as a viable therapeutic target, partly because HDL-C does not reflect high-density lipoprotein (HDL) function. Mendelian randomization analyses that have found no evidence of a causal relationship between HDL-C levels and cardiovascular risk have decreased interest in increasing HDL-C levels as a therapeutic target. HDLs comprise distinct subpopulations of particles of varying size, charge, and composition that have several dynamic and context-dependent functions, especially with respect to acute and chronic inflammatory states. These functions include reverse cholesterol transport, inhibition of inflammation and oxidation, and antidiabetic properties. HDLs can be anti-inflammatory (which may protect against atherosclerosis and diabetes) and proinflammatory (which may help clear pathogens in sepsis). The molecular regulation of HDLs is complex, as evidenced by their association with multiple proteins, as well as bioactive lipids and noncoding RNAs. Clinical investigations of HDL biomarkers (HDL-C, HDL particle number, and apolipoprotein A through I) have revealed nonlinear relationships with cardiovascular outcomes, differential relationships by sex and ethnicity, and differential patterns with coronary versus noncoronary events. Novel HDL markers may also have relevance for heart failure, cancer, and diabetes. HDL function markers (namely, cholesterol efflux capacity) are associated with coronary disease, but they remain research tools. Therapeutics that manipulate aspects of HDL metabolism remain the holy grail. None has proven to be successful, but most have targeted HDL-C, not metrics of HDL function. Future therapeutic strategies should focus on optimizing HDL function in the right patients at the optimal time in their disease course. We provide a framework to help the research and clinical communities, as well as funding agencies and stakeholders, obtain insights into current thinking on these topics, and what we predict will be an exciting future for research and development on HDLs.
低高密度脂蛋白胆固醇(HDL-C)是一种致动脉粥样硬化的血脂异常,反映了不良的生活方式选择、代谢受损和心血管风险增加。低 HDL-C 也与炎症性疾病、恶性肿瘤、糖尿病和其他疾病的风险增加有关。这种流行病学证据并没有转化为提高 HDL-C 作为一个可行的治疗靶点,部分原因是 HDL-C 不能反映高密度脂蛋白(HDL)的功能。孟德尔随机分析发现,HDL-C 水平与心血管风险之间没有因果关系的证据,降低了人们对提高 HDL-C 水平作为治疗靶点的兴趣。HDLs 由不同大小、电荷和组成的颗粒组成,具有多种动态和依赖于上下文的功能,特别是在急性和慢性炎症状态下。这些功能包括胆固醇逆转运、抑制炎症和氧化以及抗糖尿病作用。HDLs 可以是抗炎的(这可能有助于预防动脉粥样硬化和糖尿病)和促炎的(这可能有助于清除败血症中的病原体)。HDLs 的分子调控很复杂,这体现在它们与多种蛋白质以及生物活性脂质和非编码 RNA 的关联上。对 HDL 生物标志物(HDL-C、HDL 颗粒数和载脂蛋白 A 至 I)的临床研究揭示了与心血管结局的非线性关系、性别和种族的差异关系以及与冠状动脉与非冠状动脉事件的差异模式。新型 HDL 标志物也可能与心力衰竭、癌症和糖尿病有关。HDL 功能标志物(即胆固醇流出能力)与冠心病相关,但它们仍然是研究工具。操纵 HDL 代谢的治疗方法仍然是圣杯。没有一种方法被证明是成功的,但大多数方法都针对 HDL-C,而不是 HDL 功能的指标。未来的治疗策略应侧重于在正确的患者、在其疾病过程的最佳时间优化 HDL 功能。我们提供了一个框架,帮助研究和临床社区以及资助机构和利益相关者了解这些主题的当前思路,以及我们预测的 HDL 研究和开发的令人兴奋的未来。