HDL cholesterol and ASCVD risk stratification: A debate

被引:47
作者
Barter, Philip [1 ]
Genest, Jacques [2 ]
机构
[1] Univ New South Wales Kensington, Sch Med Sci, Lipid Res Grp, Kensington, NSW, Australia
[2] McGill Univ, Hlth Ctr, Royal Victoria Hosp Montreal, Montreal, PQ H4A 3J1, Canada
关键词
HIGH-DENSITY-LIPOPROTEIN; APOLIPOPROTEIN-A-I; CORONARY-HEART-DISEASE; ESTER TRANSFER PROTEIN; CARDIOVASCULAR OUTCOMES; INDUCED ATHEROSCLEROSIS; EFFLUX CAPACITY; CETP ACTIVITY; METABOLISM; MORTALITY;
D O I
10.1016/j.atherosclerosis.2019.01.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This debate is designed to review the usefulness of the cholesterol mass within high-density lipoproteins (HDL-C) to predict the risk of atherosclerotic cardiovascular disease (ASCVD). Pro: There is much current confusion regarding the role of high density lipoproteins (HDLs) in atherosclerotic cardiovascular disease (ASCVD). While it is an established fact that the concentration of HDL cholesterol is a robust, independent, inverse predictor of the risk of having an ASCVD event, recent studies have questioned whether HDLs actually protect against ASCVD. But this in no way challenges that fact that the concentration of HDL cholesterol is a powerful tool to be used in risk stratification of ASCVD. Con: The measurement of HDL-C in the 1970 heralded a new area of promising and exciting research in cardiovascular disease. The measurement of HDL-C has been part of cardiovascular risk stratification for the past three decades. HDL have pleotropic beneficial effects on the arterial vasculature and promote the removal of excess cholesterol from lipid laden macrophages. These effects are only weakly Arelated with HDL-C levels. While HDL-C is associated with atherosclerotic cardiovascular disease, the epidemiological relationship falters at the extremes of measurement. Mendelian randomization does not support a link of causality and to date, attempts to raise HDL-C pharmacologically have not yielded the expected outcomes. The time has come to consider abandoning HDL-C for cardiovascular risk prediction and clinical decision making and to double efforts to develop better biomarkers of HDL function.
引用
收藏
页码:7 / 12
页数:6
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