Does Elevated High-Density Lipoprotein Cholesterol Protect Against Cardiovascular Disease?

动脉粥样硬化性心血管疾病 内科学 孟德尔随机化 医学 内分泌学 血脂异常 胆固醇转移蛋白 胆固醇 脂蛋白 高密度脂蛋白 疾病 生物 生物化学 遗传变异 基因型 基因
作者
Alexander C. Razavi,Vardhmaan Jain,Gowtham R. Grandhi,Parth Patel,Angelos Karagiannis,Nidhi Patel,Devinder S. Dhindsa,Chang Liu,Shivang Desai,Zakaria Almuwaqqat,Yan V. Sun,Viola Vaccarino,Arshed A. Quyyumi,Laurence Sperling,Anurag Mehta
出处
期刊:The Journal of Clinical Endocrinology and Metabolism [The Endocrine Society]
被引量:2
标识
DOI:10.1210/clinem/dgad406
摘要

High-density lipoprotein (HDL) contributes to reverse cholesterol transport, which is one of the main explanations for the described inverse association between HDL-cholesterol (HDL-C) and atherosclerotic cardiovascular disease (ASCVD) risk. However, efforts to therapeutically raise HDL-C levels with niacin, fibrates, or cholesteryl ester transfer protein inhibitors have not demonstrated a reduction in ASCVD events when compared to placebo among individuals treated with statins. Furthermore, mendelian randomization studies suggest that HDL-C is unlikely to be a direct biologic variable impacting ASCVD risk. More recently, observations from well-conducted epidemiologic studies have indicated a non-linear U-shaped relationship between HDL-C and subclinical atherosclerosis, and that very high HDL-C (≥80 mg/dL in men, ≥ 100 mg/dL in women) is paradoxically associated with higher all-cause and ASCVD-related mortality. These observations suggest that HDL-C is not a universal protective factor for atherosclerosis. Thus, there are several opportunities for reframing the contribution of HDL-C to ASCVD risk and related clinical calculators. Herein, we examine our growing understanding of HDL-C and its role in ASCVD risk assessment, treatment, and prevention. We discuss the biological functions of HDL-C and its normative values in relation to demographics and lifestyle markers. We then summarize original studies that observed a protective association between HDL-C and ASCVD risk and more recent evidence indicating an elevated ASCVD risk at very high HDL-C levels. Through this process, we advance the discussion regarding the future role of HDL-C in ASCVD risk assessment and identify knowledge gaps pertaining to the precise role of HDL-C in atherosclerosis and clinical ASCVD.
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