HDL biology
Review names CETP inhibition as an emerging strategy for HDL-targeted cardiovascular drug development (Nat Rev Drug Discov 2005)
Original title: HDL as a target in the treatment of atherosclerotic cardiovascular disease
This review argues that statins' LDL-lowering benefit has limits, motivating growing interest in HDL cholesterol as an additional cardiovascular drug target. It examines the mechanisms underlying HDL's protective effect and surveys several emerging strategies for raising HDL cholesterol to treat cardiovascular disease: nuclear receptor modulation, inhibition of cholesteryl ester transfer protein, and infusion of apolipoprotein/phospholipid complexes. CETP inhibition is presented as one of the small number of named pharmacological approaches to HDL-raising therapy under active development at the time.
Original abstract
Lipid abnormalities are among the key risk factors for cardiovascular disease. Indeed, lipid-modifying drugs - in particular, the statins, which primarily lower plasma levels of low-density lipoprotein (LDL) cholesterol - considerably reduce the risk of cardiovascular events, leading to their widespread use. Nevertheless, it seems that there might be limits to the degree of benefit that can be achieved by lowering LDL-cholesterol levels alone, which has led to increased interest in targeting other lipid-related risk factors for cardiovascular disease, such as low levels of high-density lipoprotein (HDL) cholesterol. In this article, we first consider the mechanisms that underlie the protective effect of HDL cholesterol, and then discuss several strategies that have recently emerged to increase levels of HDL cholesterol to treat cardiovascular disease, including nuclear receptor modulation, inhibition of cholesteryl ester transfer protein and infusion of apolipoprotein/phospholipid complexes.
HDL biologymechanismspharmacology
Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 19 August 2026. Methods.