Quo Vadis after AEGIS: New Opportunities for Therapies Targeted at Reverse Cholesterol Transport?

被引:0
作者
Lan, Nick S. R. [1 ,2 ]
Watts, Gerald F. [1 ,3 ,4 ]
机构
[1] Univ Western Australia, Med Sch, Perth, Australia
[2] Fiona Stanley Hosp, Dept Cardiol, Perth, Australia
[3] Royal Perth Hosp, Dept Internal Med, Perth, Australia
[4] Royal Perth Hosp, Dept Cardiol, Perth, Australia
关键词
Cardiovascular diseases; Coronary artery disease; Dyslipidaemia; Lipid-lowering therapy; Risk factors; Cholesterol; HIGH-DENSITY-LIPOPROTEIN; APOLIPOPROTEIN-A-I; TRANSFER PROTEIN-INHIBITION; CORONARY-HEART-DISEASE; CARDIOVASCULAR EVENTS; HDL CHOLESTEROL; FAMILIAL HYPERCHOLESTEROLEMIA; MIMETIC CER-001; ATHEROSCLEROSIS; RISK;
D O I
10.1007/s11883-025-01281-3
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Purpose of ReviewHigh-density lipoprotein (HDL) is integral to reverse cholesterol transport (RCT), a process considered to protect against atherosclerotic cardiovascular disease (ASCVD). We summarise findings from the recent AEGIS-II trial and discuss new opportunities for HDL therapeutics targeted at RCT.Recent FindingsMendelian randomisation studies have suggested a causal association between the functional properties of HDL and ASCVD. However, the AEGIS-II trial of CSL112, an apolipoprotein A-I therapy that enhances cholesterol efflux, did not meet its primary endpoint. Exploratory analyses demonstrated that CSL112 significantly reduced ASCVD events among participants with a baseline low-density lipoprotein (LDL)-cholesterol >= 100 mg/dL, suggesting that RCT may depend on LDL-cholesterol levels.SummaryThe role of HDL therapeutics in patients with familial hypercholesterolaemia, inherited low HDL-cholesterol and impaired HDL function, especially with inadequately controlled LDL-cholesterol, merits further investigation. The treatment of patients with monogenic defects in HDL metabolism remains a significant gap in care that needs further research.
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页数:12
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