New Therapeutic Approaches to the Treatment of Dyslipidemia

被引:62
作者
Rader, Daniel J. [1 ,2 ,3 ]
机构
[1] Univ Penn, Perelman Sch Med, Dept Genet, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Dept Med, Philadelphia, PA 19104 USA
[3] Univ Penn, Perelman Sch Med, Inst Translat Med & Therapeut, Philadelphia, PA 19104 USA
关键词
HIGH-DENSITY-LIPOPROTEIN; CORONARY-HEART-DISEASE; HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA; CHOLESTEROL EFFLUX CAPACITY; PLACEBO-CONTROLLED TRIAL; ESTER TRANSFER PROTEIN; RANDOMIZED CONTROLLED-TRIAL; SUBTILISIN/KEXIN TYPE 9; OF-FUNCTION MUTATIONS; APOLIPOPROTEIN-A-I;
D O I
10.1016/j.cmet.2016.01.005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dyslipidemia is a risk factor for atherosclerotic cardiovascular disease (ASCVD). Abundant data indicate that low-density lipoproteins (LDL) are causal for ASCVD; a new class of LDL-lowering medicines, the PCSK9 inhibitors, will address much unmet medical need. Human genetics suggest that triglyceride-rich lipoproteins (TRL) are pro-atherogenic and have pointed to a number of protein regulators of lipoprotein lipase activity that are candidates for therapeutic targeting. Finally, high-density lipoprotein (HDL) cholesterol does not appear to be causally associated with protection from ASCVD, reinforced by the failure of three CETP inhibitors in CV outcome trials, but HDL function remains of interest.
引用
收藏
页码:405 / 412
页数:8
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