The class
Review questions whether elevated HDL cholesterol truly protects against cardiovascular disease (J Clin Endocrinol Metab 2024)
Original title: Does Elevated High-Density Lipoprotein Cholesterol Protect Against Cardiovascular Disease?
This review examines the evolving understanding of HDL cholesterol (HDL-C) and cardiovascular risk. It notes that therapeutic efforts to raise HDL-C with niacin, fibrates, or cholesteryl ester transfer protein (CETP) inhibitors have not reduced atherosclerotic cardiovascular disease (ASCVD) events compared with placebo in statin-treated patients, and that Mendelian randomisation studies suggest HDL-C is unlikely to be a direct causal factor in ASCVD risk. The authors highlight epidemiologic evidence of a nonlinear, U-shaped relationship between HDL-C and subclinical atherosclerosis, with very high HDL-C (80 mg per dL or more in men, 100 mg per dL or more in women) paradoxically associated with higher all-cause and ASCVD mortality. The review argues these findings warrant reframing HDL-C's role in cardiovascular risk assessment and clinical calculators.
Original abstract
High-density lipoprotein (HDL) contributes to reverse cholesterol transport, which is 1 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 with 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 nonlinear 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. Here, 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.
Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 19 August 2026. Methods.